2024 INFORMATION QUANTA

What did I teach you about long ago about how polar bears and penguins repel cold temperatures so they can live in polar water? How did they do it?  Why do we struggle with it??   What do they both eat, and where do they both live?  What is special about that environment?  Is there something special about these animals compared to us?  Do you sense an entanglement yet with these concepts? A food guru will struggle to see the gorgeous threads nature provides living quantum systems. A mitochondriac will begin to see something different.

DO NOT COMPLY WITH CONVENTIONAL WISDOM OR LOGIC BECAUSE AT THE QUANTUM LEVEL, THE TRUTH WILL EVADE YOU.

The invisible threads nature weaves into electron and proton spin are the strongest ties in the quilt of our lives.   Today, this installation from the QUILT is about the foundations of thermodynamics in living systems.  How these new concepts link to the quantum spin states of electrons and protons in mitochondria is critical to get correct before we can see nature’s wisdom manifest in tissues.

The aftermarket data of the COVID-19 vaccines show this to us all now, but few people see this lesson.  You must do so at the dawn of 2024.

People normally understand the law of increasing entropy as the tendency for things to get messier as time evolves. Still, the truth is stranger than fiction because it often makes no sense when you do not have all the data about the system in question. Still, science and mathematics now report that entropy actually leads to order in nature.  Dr. Mike Levin is looking under this specific rock constantly in his lab.  When he gets to this level, he’ll begin to understand how regeneration and morphogenesis operate using subatomic particles and light.

The philosopher steeped in epistemology will say, “Uncle Jack, why is this idea you are presenting to us at the beginning of 2024 not a thermodynamic paradox?”

Nature organizes living quantum systems using nothing but entropy.

Order in biology always emerges from DISORDER.

At its core, nature is asymmetric because of its atomic design.

The experiment I did above shows you this effect in real time.  What allows them to assume this pattern?  Is it a chemical bond?  Is it a hydrogen bond?  Is it electrostatics?  Is it some quantum effect?  No, it is none of those things.  The pattern emergence comes from the entropy I introduced into the system through the crafty knife cuts I put on all the pieces as I put them in the pan.

What is in the pan?  The organization of matter in the geometry of time and space gives matter a morphogenesis, an appearance.  What if I told you that altering the spin state of atoms creates order?  Would you believe it?

Many phenomena in self-organizing systems are interpreted in the centralized literature as navigation in a morphological space.

The concept of morphological space can describe the range of physical forms a species can exhibit in Nature.  The chaos in light can self-organize the things in matter to create a form.  In this way, light frequency is information.  Once light hits matter, it can be transformed into sound, which can be used to transform matter.

By navigating this space, the organism changes shape over time. Both morphogenesis and damage repair processes can be thought of as navigating this morphological space toward the stable adult form of the organism. Magnetism is a key way life gains its size and shape.  Free radicals are magnetic.  Most proteins in us act like semiconductors and are paramagnetic.  This means they are drawn to magnetic fields.  These small pieces of matter are like algorithms with instructions to rebuild the form.  The damage becomes impossible to heal for the organism if it is at a point in the morphological space outside the basin of attraction of the stable configuration.

Sonic Hedgehog and Vitamin A begin the regeneration process in almost all phyla.  They are also critical in morphogenesis.

The simplest example of self-organization is called the Ising Model in physics.

This model confounds food gurus.  The model acts as follows:  Mother Nature is informing the food gurus and biochemists that every day, she eats a bowl of the alphabet soup of atomic spins from the environment, and this causes her to shit out better questions than any modern centralized guru could propose.  What she is doing below the cell level is beyond their ability to fathom because of how they see the world.   

But what exactly is the Ising model?

Originally it was conceived as a simple explanation for magnetization effects in matter, the Ising model explores the interplay between interacting spins. When in proximity, these spins tend to align with each other, leading to an interaction energy denoted by H=−Js1⋅s2H=−Js1​⋅s2​.

When something becomes magnetized, spins are aligned, and the atomic lattice consumes energy; this gives it its form.  The addition of energy can change this form.  Light energy and temperature energy do this to cells in a circadian fashion.

What happens when lots of spins interact all at once in matter? Well, it depends on how they interact: The Ising Model comes in many different flavors that begin to help us understand how order comes from chaos.  Watch this video to understand how this operates in nature below your ability to sense it.  This is why Nature is hard to understand for food gurus and biochemists.  Mother Nature acts to levitate and fall asleep inside our atomic structure to drive what tissues are capable of.

VIDEO OF HOW THIS IDEA CHANGES HOW THINGS APPEAR

VIDEO 2 is for the deep physics geeks.

In my opinion, why do all cells release ELF-UV?

UV light magnetizes matter easily to alter its spin state.  Many organic syntheses are substantially accelerated and decelerated or made possible in the first place by exposure to UV radiation.  Mother Nature knew this 3.6 billion years ago.  She used IR/heat in mitochondria to favor the spin choice of H+ over deuterium in certain locations in cells, and she allowed cells to release ELF-UV collected from sunlight to control both redox and detox action within cells because purple light harnessed from the sun knows how to clean up after itself with a small mess.

The Functional medicine food guru doctors have no idea this is how the process works because if they did, they would never offer sham detox/chelation programs to patients. The smart move is to put patients in sunlight, allow them to absorb UVA and UVB in a coupled thermodynamic fashion, and bury those frequencies in the topologic insulators inside cells.

SUMMARY

You must learn the lesson of how we got to the idea that the spins of the subatomic world and how light can change them, and the charge of atoms can drive regeneration and morphogenesis programs in us.

Democritus is the key hero in the story.  He is mostly remembered today for formulating an atomic theory of the cosmos.  Much of his work has not survived.  What remained are anecdotes attributed to his ideas.  This idea is beautiful because quantum mechanics has not yet been broadly applied to biology.

One of Democritus’ arguments supporting atomism was that atoms naturally explain the sharp phase boundaries observed in materials, as we see when ice melts to water or water turns to steam. His idea was that small changes in atomic-scale properties would lead to big changes in the aggregate behavior. This defines the butterfly effect of Lorenz. Others believed that matter is inherently continuous, not atomic and that the large-scale properties of matter are not reducible to basic atomic properties.

While the laws of chemical bonding made it clear to nineteenth-century chemists that atoms were real, the debate continued well into the early twentieth century among physicists. Atomists, notably James Clerk Maxwell and Ludwig Boltzmann, applied Hamilton’s formulation of Newton’s laws to large systems and found that the statistical behavior of the atoms correctly describes room-temperature gases. However, classical statistical mechanics did not account for all the properties of liquids, solids, or gases at low temperatures.

Once modern quantum mechanics was formulated in the early 20th century, atomism was no longer in conflict with real experiments in the lab, but this still did not lead to a universal acceptance of statistical mechanics, which went far beyond atomism.

Josiah Willard Gibbs had given science a complete formalism to reproduce the laws of thermodynamics from the laws of mechanics. However, many faulty arguments have survived from the 19th century, when statistical mechanics was considered dubious by the paradigm of thought in power. The lapses in intuition mostly stemmed from the fact that the limit of an infinite statistical system has many zero-one laws which are absent in finite systems: an infinitesimal change in a parameter can lead to big differences in the overall aggregate behavior, as Democritus expected.

This enigma remains today in the self-organization of cells that defines how chaos becomes order when small things in cells begin to exert their effect, on the whole, to define what the cell is capable of physiologically.  This is the edge of modern developmental biology on January 1, 2024.

THE YEAR IN CIRCADIAN REVIEW………..2023 key papers

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A day in your life on Earth is just a collection of hours, but a life to a person is a collection of memories that build a coherent wisdom.  It requires you to be awake during the day and asleep when the sun is absent.  This rule is axiomatic for diurnal mammals.  The final blog of 2023 brings you the best papers to illuminate the ideas in this opening paragraph.

Why is melanopsin/retinol key to understanding all human disease? In physics, time in itself, absolutely, does not exist; it is always relative to some observer or some object because of how light builds it. Without a clock I say ‘I do not know the time’. You do not. This is why evolution built one in the SCN and uses melanopsin and retinol to control the peripheral clock genes to drive renovation. The SCN clock must run fast than the melanopsin mechanism to make sense of the chaos around us.

The implications of this statement are far reaching. Without matter time itself is unknowable. Time is a function of matter; and matter therefore is the clock that makes infinity real. This is why the time crystals in you are coded for DNA. If you ask me, the brain, in fact all neuroectoderm was innovated by evolution to tell time. I think it is the single most important function of the nervous system.

Time is a function of how entropy flows and entropy flows according to how heat flows in a system. Mitochondria create heat when they are irradiated by light. Clocks become more accurate the higher periodicity they have. Daily & seasonal light alters the circadian periodicity of clock genes. The diurnal changes of sunlight from sunrise to sunset change the amount of water made in your mitochondria. Sunlight creates water.

Biology is so difficult to explain without understanding what light is doing at the subcellular level. What an impressive cycling process like a multifunction relay signaling flow switch multiplied to reduce. Wouldn’t it be so much easier to just use numbers. Then everyone would get it crystal clear even the fifth grader.

1. Sato and Sato said in their July 2023 paper that “the circadian regulation of metabolism for health and disease, “dominates” metabolic homeostasis =  light trumps food.  Imagine that.

https://academic.oup.com/endo/article-abstract/164/7/bqad086/7186648

2. Light disrupts clock gene BMAL1.  CLOCK and BMAL1 are positive regulators of circadian gene expression, and PER and CRY are the negative regulators that operate under day and night cycles.

And in a curious feed-forward mechanism, CLOCK and BMAL1 enhance SIRT1 expression… genetic deletion of any of these players induces insulin resistance.  Indoor life under manufactured light decrease SIRT 1 causing insulin resistance.  No food needed.  Do you hear that?

Did you know in in 2023 we found out that the very same core clock gene, Bmal1,that impaired glucose absorption in the intestine in mice also happens in humans?  No food needed.  Just bad light can do it.  This goes on to affect systemic glucose homeostasis.  Imagine that.  https://academic.oup.com/endo/article/163/9/bqac119/6651710

3.  SIRT 1 lowers with INDOOR living.

Why is this a big deal?

NAD+ is one of the more immediate players in cytochrome 1 that is a huge driver of circadian biology in humans.  It is the coenzyme called nicotinamide adenine dinucleotide (NAD+). It participates in a variety of redox reactions in the matrix that help generate DDW.  Solar exposure and fasting work with light frequencies to slow ECT flow and this can increase the intracellular NAD/NADH ratio if the light environment is dominated by sunlight.  It won’t do this with artificial light.  It lowers NAD+.  This is what sets off a cascade of circadian events that can destroy tissues because they involve epigenetics and the regulation of growth and metabolism of man.  LIGHT DOES THIS.  NOT FOOD OR FUELS.

SUN + fasting -> NAD+ -> SIRT1 -> BMAL1/CLOCK -> NAMPT -> NAD+

NAD+ major effect is to activate the sirtuins as the reaction above shows.  This is a family of deacetylase enzymes.  When you understand what UV and IR light are doing to a matrix, you can see why fasting could potentially be seen as a circadian reset biohack.  It won’t work in fake light when ALAN is present.

SIRT1 also activates PGC1a in liver (Rehan et al., 2014), which enhances fatty acid oxidation, at a time when HUMANS require it during sleep in the absence of ALL light at night.   https://www.frontiersin.org/articles/10.3389/fnmol.2018.00496/full

4. Centralized scientism relies on mice studies to create beliefs they hold to be truthful as part of the dogma.  Did you know despite the importance of the mouse in centralized research, the levels of circulating gonadal steroids across the estrous cycle are not established with any temporal precision?  True.  The observations made in the study once again prove the decentralized axiom that you can never learn the truth from lab mice without light controls.  Why?  The paper provided the first detailed assessment of fluctuating gonadal steroid and reproductive hormone levels across the mouse estrous cycle and it indicated that species differences exist between mice and other spontaneously ovulating mammalian species.  Imagine that.  https://academic.oup.com/endo/article/164/6/bqad070/7159815

5. Many textbooks on biochemistry and endocrinology will tell you growth hormone is released during slow wave sleep.  It is simply not true.  POMC controls it in the medial basal hypothalamus.

GH-releasing hormone (GHRH) and somatotropin release-inhibiting factor (SRIF; somatostatin). GHRH stimulates GH release whereas SRIF inhibits GH. Human males exhibit life long ‘pulsatile’ secretion versus female’s who exhibit a ‘continuous’ secretion from their somatotrophs.  One sex continuously makes endogenous UV light biophontons in the hypothalamus and one does not.   UV light stimulates POMC translation and cleavage.

  • Slow waves (SWs) are thought essential for sleep-dependent recovery processes.
  • Their amplitude, incidence, frequency and slope reflect synaptic strength.
  • Their regulation has been postulated to be independent of circadian phase by centralized dogma.
  • We now have data below that all characteristics of SWs depend on circadian phase control of the SCN

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503801/

When melanin is degraded by hypoxia it becomes norepinephrine and dopamine.   Norepinephrine decreases GH secretion by increasing the release of somatostatin. This central effect, due to the activation of α1-adrenergic receptors, has been demonstrated in mammals.

Dopaminergic agonists have been shown to increase GH release, as well as to decrease hypoglycemia-, levodopa-, and arginine-induced increases in GH release. Because dopamine can increase both GHRH and somatostatin release, it appears that this balance can change under different physiological conditions.  Light stress is critical here.

The dorsal longitudinal fasciculus (QE #47) is found within the dorsal brainstem tegmentum. It passes through the periaqueductal gray matter and contains both ascending and descending fibers.

The ascending fibers pass from the reticular formation (sleep center) passing to the hypothalamus thus transmitting information related to the viscera. In turn, the descending portion arises also from the hypothalamus and passes to a variety of brain areas responsible for processing pain, cardiorespiratory functions and the autonomic system. Finally, the efferent fibers will also terminate on the preganglionic fibers of the autonomic nervous system.

https://academic.oup.com/jes/article/6/11/bvac146/6702162

6.  Kids with high risk type 2 diabetes should have their urine assessed for circadian dysruption.  When melanin degrades internally more catecholamines are made and this will be filtered through the kidneys.  Urinary catecholamines are a great marker endogenous melanin destruction.

https://academic.oup.com/jes/article/7/2/bvac190/6889558

7. Why is shift work always associated with metabolic issues in humans?  Experimental circadian misalignment data have shown minimal effects on steroidogenesis at the adrenal gland level.    The same was not true of the sex steroids.  This is why gonadal cancers occur so often in shift workers. This dichotomy also predisposes night-shift workers to metabolic ill health. The decentralized clinician should always look at  the adrenal steroid cascade, including cortisol and the main adrenal androgen 11-ketostosterone.  Why?  It should always be evaluated during the biological morning in the case of shift workers because testosterone and estrogen, are highly dependent on the shift-work schedule.  https://academic.oup.com/jes/article/6/12/bvac153/6731224

PCOS is characterized by a constellation of interrelated reproductive abnormalities, including disordered gonadotropin secretion, increased androgen production, chronic anovulation, and polycystic ovarian morphology. It is frequently associated with insulin resistance and obesity. These reproductive and metabolic derangements cause major morbidities across the lifespan, including anovulatory infertility and type 2 diabetes (T2D).  Most centralized textbooks report PCOS has no known cause.  Shift work and light and night are the main offender.  The paper above explains why it happens.  No more mystery for PCOS ladies.  Turn the lights off after sunset and avoid all nnEMFs.  In Endocrine Reviews this year, authors Dapas and Dunaif discussed these insights

8.  Type 1 diabetic women teach us a lot about how light controls female oocyte behavior.

Often modern women living with type 1 diabetes complain of changes in glucose values according to the different phases of menstruation. This has been confirmed in several studies showing that the glycemic pattern varies according to the different phases of menstrual cycle in most women with T1D.  Why?  Did you know that menstuation links to NO and blood glucose variations in the capillary bed?

The moon used to control the reproductuve cycle in humans.  Artificial light from fire onward effectively extinguished this link in modern women.  Can we still experience the real effect in a disease model?  Yes.  Type 1 diabetic women show the effect because they have no light controls.  Normal non diabetic women experience a transient pregnenolone steal syndrome to stimulate ovulation.  This is how a light stress event every month was used by biology to control fertility timing.

Lunar cycles modulate the estrus cycle of many mammals because the moon can and does reflect blue light from the sun at night to the Earth as it goes through its revolutions monthly around Earth.  That is why they influence woman’s hormone cycles assuming she is properly connected to Earth, sun and the lunar cycles. MOST ladies aren’t properly coupled, therefore, their hormone effects are muted and lowered in modern females. This is why estrus has vanished in modern humans and proof it still has influence can be seen when women get together and live together their cycle will all become coupled oscillator again, just like molecular resonance theory predicts. When the negative and positive feedback loop in the circadian mechanism is uncoupled from one another the result is the extinction of both sides of the coupled system. This extinction effect manifests in the pregnenolone steal syndrome.  Look at the link of T1D to latitude below.

In high latitudes cold stimulates increasing blood glucose over time.

In T1D women glucose levels rise linearly throughout the menstrual cycle, reaching a maximum in the late luteal phase. Then a sharp decrease was seen for most participants at the beginning of menstrual bleeding.  This links light blood glucose to the lunar cycle because of how light varies.

T1D human females and corals teach us how important light is to fecundity.  Remember fecundity in humans is controlled by the leptin melanocortin pathways.

Among all, probably the most spectacular and documented event orchestrated by animals according to the lunar cycle is certainly the mass spawning of corals. Like inside a shaken snow globe, once every year, the barrier reef explodes of eggs and sperms, few days after Full Moon, during late spring/summer nights, a phenomenon even visible from space. Unfortunately, reef corals are losing this critical reproductive synchrony, due to the anthropogenic impact of artificial light at night. This phenomenon threatens several species, not only corals but entire reef communities.  This is why modern infertility in humans is increasing as well.

Starting with the beginning of the last century, a multitude of scientific studies have documented that the lunar cycle times behaviors and physiology in many organisms. It is plausible that even the first life forms adapted to the different rhythms controlled by the moon. Consistently, many marine species exhibit lunar rhythms, and also the number of documented “lunar-rhythmic” terrestrial species is increasing.

Organisms follow diverse lunar geophysical/astronomical rhythms, which differ significantly in terms of period length: from hours (circalunidian and circatidal rhythms) to days (circasemilunar and circalunar cycles). Evidence for internal circatital and circalunar oscillators exists for a range of species based on past behavioral studies, but those species with well-documented behaviorally free-running lunar rhythms are not typically used for molecular studies.

Thus, the underlying molecular mechanisms are largely obscure: light reflection from of the moon varies with every day to increase blood glucose.

Lunar rhythms of light, dark, and gravitation changes cause alteration in the human transcriptome, proteome, and physiology. The proxy for these effects is seen in the hormonal variation of humans.

Most women who have circadian control experience a menstrual cycle that is connected to every new moon. And the 4 phases of the menstrual cycle seem to correspond to the 4 phases of the moon (new moon: menstruations, first quarter: follicular, full moon: ovulation and last quarter: lutheal).  https://academic.oup.com/jcem/article/107/10/2793/6648857

9.  Papers are now out showing how POMC cleavage and light cause type 2 diabetes and lead to sleep apnea.  It turns out that the steeper your diurnal cortisol slope is, it will be associated with a smaller and higher midnight cortisol levels.  As this POMC effect occurs you will see a greater risk of developing type 2 diabetes in people.  As this occurs the clinician should expect comorbid rise of hypertension and obstructive sleep apnea.  This is all due to light effects on POMC translation.  It shows you why type diabetics are created by modern light choices.  https://academic.oup.com/jcem/article/108/9/e679/7109980

10.  Neurosurgeons deal with patients with Cushing disease due to pituitary tumors.  In my 30 year career one thing I always saw in every case I dealt with was a loss of the pulsatile effects of cortisol secretion in those with a tumor.  Because of this I knew light was behind the growth of the tumor.  Now we have a paper showing you my instincts were correct.  ACTH variability is suppressed in patient with Cushing disease, and that remission of the pulsatile release of cortisol is associated with restoration of this variability.  Seeing AM and PM light helps these people recover this ability tremendously and this is why seeing the sunrise and sunset matter in POMC biology.  https://academic.oup.com/jcem/article/108/11/2812/7187942

MY 2023 CHRISTMAS LIST FOR MY TRIBE

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In this list, you will get my insight into how I treat several diseases, like autism, long covid, and cancers.

I hope you carefully watch the video above before progressing.

Winning and nature have much in common

• Winning isn’t loyal to you

• Winning doesn’t care about you •

Winning doesn’t care  how sore you are

• Winning doesn’t care  how hard you work

• Winning doesn’t care how much sleep you get, either

But this should hit you like a punch in the face from Iron Mike Tyson if you are a mitochondriac.

Are you willing to sprint when the distance is unknown because nature requires you to live by her light laws and not the ones mandated by man?

Are you willing to dig deep to discover the truth about where diseases come from, or will you be a comfortably lazy centralized human buying the story of centralized paradigms?

The annual traditions continue but with a new twist.  Everyone knows about the 12 days of Christmas as a carol.  This year, I will use the song to create a list of the DUMMIES in your life.  If you want them to be wiser than they have been, this list is for you.

1.  On the first day of Christmas, you will receive “the gift of information” from me this year. The 12 days of Christmas begin with the gift of “CHARGE.” Did you know “charge” is conserved by nature?  Quantum mechanics tells us this. Uncle Jack, is this why Astra Zeneca and JNJ jabs were associated with more clots than myocarditis in Pfizer and Moderna jabs?  Yep. The liquid nanoparticles (LNP) charge was different in each jab.

The LNP of each jab has a unique “charge” density. It can have a neutral charge, positive charge (+), or negative charge (-).   The RNA and DNA have a negative charge (-). The ionizable lipids have a positive charge (+).

How do impurities from plasmids and SV 40 cause damage?  They alter the charge, too.  Inside the  positively charged lipids inside an RNA/LNP covalently bond w/ DNA plasmids, allowing positively charged lipids to “hitch a ride” into the nucleus with the DNA (as an adduct) of cells, impacting histones (and causing frameshift mutations and aggressive cancer):

For those who think this implausible, you are wrong.  This is an interesting study related to charge changes in brain cancer. “The observed alterations in biochemical profiles upon incubation with the Pfizer/BioNT in the specific organelles of the glial cells are similar to those we observe for brain cancer vs grade of aggressiveness.” HYPERLINK

Impurities in Positively Charged Lipids in the LNP can MUTATE mRNA in LNP (Packer et al., 2021), potentially mutating other nucleic acids (RNA, DNA) that could lead to: -Point mutation -Aberrant Protein (toxic) -Noncoding (can be oncogenic) -Misfold that protein/aggregation.

Any RNA impacted would not express protein properly. Could cause cellular toxicity and immunogenicity. Reaction with nucleic acids can lead to gene mutation/carcinogenesis. An aberrant protein can have altered amino acid sequences, folding patterns, and functional properties.  Partial Translation or Misfolding: truncated proteins or proteins with missing functional domains can lead to disease and oncogenesis.  This could impact human RNA/DNA if it comes in contact. Positively charged lipids may enter the nucleus if contaminated with DNA. HYPERLINK

Electrons are negatively charged protons, and deuterium is positively charged.   Charge density actually determines where in the body it goes and what it does.   This is basic redox chemistry at work in your tissues. It’s why I see so many clots in brains irradiated by blue light RF and microwaves from tech devices some humans abuse.

Bonus gift on day one:  did you know nnEMF alters charge in different octaves of the electromagnetic spectrum?  Guess which one neutralizes charge best?  Visible spectrum octave. Imagine that. Might this be why Corona = sun is linked to the family of viruses tied to this shit storm created by Fauci et al. In Wuhan and Ukraine bioweapon labs?

Evil done with good intent is bottomless.

SO WHAT DID FAUCI et al. ORGANIZE IN WUHAN AND UKRAINE?

Anything with an altered negative charge in humans usually appears first in the lungs, then blood, and then the brain. Ask any ER doctor what the progression of death march for clots in Emergency rooms post mandate. Answer you’ll get:  first, we saw Pulmonary Embolisms, then we saw clots in weird vessels, and now we see 7-13 brain bleeds a week like this one below in a 43-year-old vegan bodybuilder.

This is the epidemiological window of how altered redox changes in mammals with variable mitochondrial capacity in organs. It is the quantum mechanics of charge loss at a tissue level because charge is a physical trait that is conserved by Nature.

2.  On the second day of Christmas, my true love gave to me, a circumpolar flight.   How does charge work on planes?

What other things do humans do that alter charge fast and do similar things?  Ever taken a circumpolar flight through a proton shower and seen an aurora?  Yep. Ask Carrie Fisher how that worked out.  There are lessons everywhere in Nature if your mind is open. Remember, the fruit doesn’t magically appear immediately when you plant seeds. So it is with health and disease.

Hey, can you ground well when you fly?  NOPE.   Grounding is how we transfer charge from the sun to Earth and into us.  We must have melanin, water, and other batteries in us to hold the charge.  You will learn about them below.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378297/

3. Whether we realize it or not, we carry in our mouths the legacy of our evolution under the power of Mother Nature. Our teeth are like living fossils that can be studied and compared to those of our ancestors to teach us how we became human.   You may not know that transitioning from yesterday’s ignorance, misapprehension, and superstition to today’s enlightened and nerve-deadened protocols has been a long, slow, and very painful process for me.

I want to share a story relayed to me by an ENT specialist.

Lindsey Hanes burst into tears at the wheel of her black Dodge Caravan when she left her son’s doctor appointment. It was ugly crying that many people saw in the parking lot. Heaving sobs. Through raindrops on her car window, she glanced back at the medical building she’d just exited. That therapist in the ENT office had been her last hope to address her son Micah’s sleep and breathing problems. Her sweet, cheerful baby had transformed into a withdrawn, ornery, uncooperative 5-year-old. As a registered “nighttime ICU nurse,”   The picture below really explains Micah’s real problem.

Hanes felt convinced that sleep deprivation lay at the root of his problems. He snored, tossed and turned at night, and woke up with bags under his eyes. At age 4, Micah underwent a sleep study and received a diagnosis of apnea — intermittent waking due to a blocked airway. The ENT surgeon she just left removed Micah’s tonsils and adenoids, and the operation seemed to work initially: Fluid no longer collected in his ears, previously a recurring problem. But a year later, he still snored — a possible sign of continued airway obstruction. It was back to the ear-nose-throat doctor, who ruled out apnea after a second sleep study. The ENT offered no other ideas. Desperate, Hanes tracked down the only myofunctional therapist in her state trained in teaching tongue and lip exercises that might reshape Micah’s mouth muscles. Maybe that would facilitate better breathing and sleep.

Micah behaved wildly in the appointment, jumping all over the chair and hiding behind Hanes. He refused to let the therapist look in his mouth, no matter how she coaxed or tried to engage his interest. By the end of the appointment, Hanes felt sweaty and exhausted, a familiar experience. She apologized profusely to the therapist, who declined to charge the family. Hanes trudged back to her car with Micah, where she dissolved into sobs. The Hanes family felt they had reached the limits of established centralized medical practice and found no cure for Micah’s sleep and breathing problems. So Hanes did what any modern parent would: she turned to Dr. Google. She discovered a whole community of decentralized researchers and Dr. Ungar’s work there.

On the third day of Christmas, we go out and buy the dummies in our life, the book “In Evolution’s Bite.”  It is written by the noted paleoanthropologist Peter Ungar.  Ungar is a personal friend of one of my classmates from dental school.  It was because of this classmate Uncle Jack wised up about fluoride, flossing, and tooth brushing.  All these ideas are superfluous under the power of sunlight and redox charge.  Why?  Ungar found thousands of ancient skulls with perfect dentitions without access to dentists, modern dentistry, and fluoridation.  It appears the ancients did not need an orthodontist either because every skull he found had a perfect class one occlusion.

WHAT HAVE CENTRALIZED PARADIGMS TAUGHT ME ABOUT MODERN LIFE AND TEETH?

For example, did you know that:
*Among the toothache remedies favored by Pierre Fauchard, the father of dentistry, was rinsing the mouth liberally with one’s own urine.
*George Washington never had wooden teeth. However, his chronic dental problems may have impacted the outcome of the American Revolution.
*Soldiers in the Civil War needed at least two opposing front teeth to rip open powder envelopes. Some men called up for induction had their front teeth extracted to avoid service.
*Teeth were harvested from as many as fifty thousand corpses after the Battle of Waterloo, a huge crop later used for dentures and transplants that became known as “Waterloo Teeth.”

Modern life is a big difference, specifically in how we live in light.  How do we know this lesson?  Egyptologists have studied the rich who lived 5000 years ago, and the slaves who lived outside in the sun and built the pyramids had perfect skulls like Ungar’s specimens, but the pharaohs who lived in temples with fire did not.  They had all the diseases modern man has.  CT scans of the mummies have confirmed this.  This might offend your beliefs.  That is good.  This is why it is on the dummy list.  I gave this very talk to the NY State Dental Society in 2013, and none of them could believe what I told you here on the third day of Christmas.

In his book, Ungar brought together cutting-edge advances in understanding human evolution for the first time with new approaches to uncovering natural clues from fossil teeth and human skulls. The result is a remarkable investigation into how teeth―their shape, chemistry, and wear―reveal how we came to be. Traveling the four corners of the globe and combining scientific breakthroughs with vivid narratives, Evolution’s Bite presents a unique dental perspective on our astonishing human development.  Teeth are neuroectodermal derivatives linked to POMC and melanin biology.  Imagine that.  No wonder the teeth respond to the energy and information in the sun.  Human teeth also fluoresce.  There are no coincidences in Nature, just lessons to stack.  Recall that melanin is made from alpha MSH, a cleavage product of POMC.

POMC is a human gene only translated when endogenous or exogenous UV is present.  Melanin has a unique ability to conduct charges simultaneously, both electronically & ionically.  When it is heated by mitochondrial metabolism, it becomes a better electronic conductor of light energy.  So, when a mother works in an ICU at night, this reduces the amount of endogenous UV light she can generate, and this loss can shrink the child’ skull, dentition, and brain in ways most cannot fathom.  Do you think nighttime ICU nurses see a lot of sun in the daytime?  Or are they sleeping when the sun is out so they can go to their job the next night?  See how this thing called NATURE works?

Charge is quantized in Nature, and it is also conserved in Nature.  POMC creates melanin from UV light so charges can be added to living tissue.  This is why Micah and millions of humans have the problems they do.  It also explains why his mom, an ICU nurse, cannot understand it.  Her education level was fully centralized.

Over the last 250 years, our skulls have morphed in dangerous and troubling ways because of our choices around light.  Our Skulls Are Out-Evolving Us because of the light we abuse to see and to eat.  Eating food out of season and eating processed food can also shrink your skull & jaws.  The same thing happened to Neanderthals when they got to the 51st latitude and began to live in caves.  Homosapiens replaced them.  Who and what are going to replace today’s dummies?  I submit to you that is what autism is really all about.  Cognitive de-evolution is here and prominent.  Re-read Patreon #45 in my Quantum Engineering series with a more serious perspective on this illuminating topic.

Last point on dentistry.  The oral microbiome folks could and should teach the gut microbiome folks a decentralized lesson in charge transfer.  No matter where the microbiome is, it should be considered a SUN in that tissue.  People forget that Fritz Popp found that prokaryotes emit 5000 times more light than eukaryotes.  This fact always told me that the skin, gut, vaginal, or oral microbiome has specific spectra of light that work with the non-visual photoreceptors used in that tissue need to transfer charges to do the physiological job of the tissues in question.

Consider the oral microbiome response to light.

Dental plaque is a biofilm that develops naturally on teeth. It consists of aggregates of 500 to 600 different bacterial taxa embedded in a matrix of bacterial and salivary origin polymers. In healthy subjects, dental plaque remains stable for prolonged periods of time because of a dynamic balance among the resident members of its microbial community. Disease arises when the microbial homeostasis within the plaque breaks down because of disruption of the habitat’s ecology.  As the microbiome changes, so does the light the prokaryotes emit.   In periodontal disease, there is a shift in the composition of subgingival plaque’s microflora that colonizes tooth surfaces and epithelial cells in the periodontal pocket to a more proteolytic gram-negative anaerobic community, including the pigmented rods in the genera Porphyromonas and Prevotella.  These bacteria change the charge density signal of the tissue.  As a result, black-pigmented anaerobes such as Porphyromonas gingivalis, Prevotella intermedia, and Prevotella nigrescens manifest in the periodontal pocket and have been implicated as pathogens associated with the initiation and progression of periodontitis.

Periodontal disease proceeds cardiovascular disease in humans.

When dental plaque samples from human subjects were irradiated with light, P. melaninogenica showed the highest susceptibility to light, followed by P. nigrescens, P. intermedia, and P. gingivalis. All of the Prevotellaspecies showed similar patterns of susceptibility to light, with growth inhibition ratios ranging between 2.1 (4.2 J/cm2) and 3.4 (21 J/cm2). The growth of P. gingivalis was inhibited 1.4 (4.2 J/cm2) to 1.9 (21 J/cm2) times.   This is an instructive lesson on how light sculpts life in your mouth.

This data on light frequency and dose are in accordance with those obtained in a previous study in which exposure of human subgingival plaque samples to red light at 633 nm led to 60 and 40% elimination of Prevotellaspecies and P. gingivalis, respectively.  The sun is 43% red in the IR-A range.

Red light from the sun or a manmade light can alter the oral microbiome. The data shows not all light is the same.  Each part of the visible spectrum has its own charge density ability.  People need to understand the microbiome provides the hierarchy of light for the tissue in question.  The hierarchy goes from wellness to disease.  Hence, bacteria act inside of us just as the sun does to living things on Earth.  It powers the local environment to action.  If it is unwell, light emission suffers, and so will the redox state of the tissue in question.  We clearly see that in periodontal disease.  This microbiome change is a predictor of future cardiac and peripheral arterial disease.  The light from one bad star in the mouth can ruin the biology in another world, the cardiovascular system.

The interesting point is that UV light is devasting to bacteria, and the dose needed to sculpt the microbiome is small.  Red light, however, is massively underpowered, giving a different effect in the hierarchy.  Within the red bands, the energy fluence delivered to the species was 360 J/cm2 since the red light corresponded to the long-wavelength absorption maximum of porphyrins. The same study demonstrated a reduction in the number of CFUs of other anaerobic and aerobic dental plaque microorganisms by 50% due to their exposure to red light in this study.

Some of the non-black-pigmented oral microbiome species use chemicals mimicking chlorophyll and hemoglobin porphyrins.  They contain porphyrins and/or other cell pigments, which can explain their susceptibility to light.

This data suggests that visible light could be used prophylactically to stabilize the normal microbial composition of plaque by suppressing potentially pathogenic BPB. Compared with other forms of periodontal therapy (scaling, mouthwashes, surgery), this form of treatment would offer many advantages: it is painless, rapid, and devoid of drug toxicity; it has no effect on taste; and it is selective in its effect.  Dentistry can and should be decentralized as well.  Let your Dummies know this.

4.  RED LIGHT DOES NOT EQUAL SUNLIGHT BECAUSE IT HAS A DIFFERENT CHARGE DENSITY.

Stop buying all the red light panel sellers telling you they are the same.  They aren’t.  This is why I do not tell you which red light is best because nothing is better than the sun.  Only 43% of the sun is red.  Is the McCullough protocol for Spike protein degradation as good as sunlight is?  NOPE.

5.  ON THE 5th DAY OF CHRISTMAS, YOU BETTER GET THE five GOLDEN RINGS I gave you here——->  https://optimalklubs.com/kruse-for-dummies-general/

These are the basics of how charge density operates in your mitochondria.  If you do not listen to it and give it to your Dummy list, you’ve failed in 2023 being decentralized.

6.  On the sixth day of Christmas, my true love gave to me……. a lesson on transition metal decentralized wisdom.   Does titanium or other heavy metals change the charge density of your tissues?  What do you know of this?  Did you know that TiO2 is being added to foodstuffs? For example, pastries, confectioneries, baked goods, toothpaste, dairy goods, cosmetics, and prescription drug coatings.  I use dentition cleaning products with baking soda and salt; they work great. You can add coconut oil if you like.  Even those organic brands hide it in their branding.  Remember, marketing is legalized lying.

Those are the most common ways people get it, but are there other ways?

Sunscreen, makeup, and medical devices.  Wait, what did you just say?  Every joint replacement,  spine surgery with implants, cardiac stents,  and most drugs and supplements carries the risk of altered charge density from Titanium. Nothing makes you bulletproof but the sun!  Did you know that melanin gets rid of heavy metals?

I hope you know that UV light from the sun creates alpha MSH from POMC to make melanin.  I also hope you remember I told you in 2023 that melanin is destroyed when tissues are hypoxic.  I hope you know that all nnEMFs outside the visible light spectrum CREATE TISSUE-LEVEL hypoxia (above pic).

Titanium is a transition metal on the periodic table……and all transition metals are dramatically attractive to microwave radiation.  This is how stars become supernovas when they begin to burn atom number 26 as a fuel source.  The red giant then blows up, which is how we get atoms above atom number 26 on the periodic table.  Nature is a furnace of creation.  She uses the electromagnetic spectrum to do it.  The same things can kill ya’ too.  Wait……what, Uncle Jack, what the hell does that mean?  Oh, you forgot what I told ya’ in 2018?

What does the EU think about Titanium?

https://efsa.onlinelibrary.wiley.com/doi/epdf/10.2903/j.efsa.2021.6585

I cannot wait until people find out what they have been doing around candy, which is going on much longer with sunscreen.

Sunscreens have massive amounts of Titanium dioxide in them, a DNA-damaging chemical. Did your experts know that?

Do they know how it links to the Melanin story? Or the melanoma story in my blogs?

For example, CereVe marketing tools tell us, “Choosing a sunscreen with gentle yet effective ingredients for all skin types—including babies’ skin and sensitive skin—is a key step in protecting your skin against sun damage. Mineral-based sunscreens commonly contain titanium dioxide (along with zinc oxide) because of this ingredient’s ability to reflect and scatter damaging UVA and UVB rays off the skin’s surface.

CeraVe offers an array of mineral sunscreens containing titanium dioxide, including hydrating sunscreen lotions for your face and body, formulas specially designed for babies, and water-resistant sunscreen sticks for touch-ups on the go. Every CeraVe SPF sunscreen product is non-greasy, helps prevent sunburn, and contains three essential ceramides to help restore the skin’s protective barrier and lock in moisture.”

Skittles, Starburst, and thousands of other sweet treats marketed to children contain titanium dioxide – an additive European food safety regulators say is no longer safe for human consumption. Yet the U.S. hasn’t reassessed the potential threats in over 50 years.  It seems like the same story around the jabs now with the FDA, right?

Titanium dioxide is used in popular candies and other processed foods to give a smooth texture or to work as a white colorant. SUNSCREENS ARE ALL WHITE GUESS WHY? White semiconductors reflect all forms of the sun. This is why melanin is black because it absorbs the frequencies of light to use it and protect cells.

The titanium and zinc pigments used in sunscreen and candy can brighten other colors, making the food more vibrant and appealing, but the additive has no nutritional benefit and harms DNA. Imagine that. Candy and sunscreen have a lot in common.

For years, some scientists have raised concerns about the potential toxicity of titanium dioxide. Its use in the U.S. continues because of regulatory folly by the Food and Drug Administration, which allows problematic ingredients to remain undetected and unreviewed. The FDA last examined the risks of the additive in 1966, but research in recent years shows there are possible health harms from titanium dioxide that warrant a fresh look from the agency.

CENTRALIZED SCIENCE IS FOS, folks.  I posted about this years ago, but y’all have short memories.  Take the Skittles out of the stockings now.

It is not just candy keto meat heads.  Do they put titanium dioxide on the outside of French cheese (like- camembert and Brie) to keep it white? YIKES

7.  On the 7th day of Christmas, your true love wants to talk about the non-visual photoreceptors in you.  Light alters the non-visual photoreceptor system because it changes the charge density of things.  This is why UV light bleaches your Sunbrella furniture.  It needs to be treated with UV-protective chemicals.  This is why blue light toxicity also drives high LDL cholesterol and low HDL levels as well. Many things blamed on poor nutrition are based on poor light environments. We have to stop blaming food for what light causes. B12 and cholesterol are two biomolecules used in the human non-visual photoreceptor cascade in cells.

More on the Christmas Dummy list: Centralized healthcare’s ignorance of the basics of this Tweet thread has led to incalculable errors for public health. I mentioned this to @RickRubin & @hubermanlab when we spoke about Dr. Changs’ belief it made 50% of what is in the textbooks obsolete. I said this on 3/4/23, so it’s been on the dummy list for a long time. It was one of the year’s biggest hits, but dummies missed it. I am telling you, 99.9% is hot garbage. Why? The number one opsin in mammals is MELANOPSIN, the human blue light detector, & we no longer live under the sun. We live in the light that killed Steve Jobs!

We live inside under LED light that destroys this non-visual photoreceptive circuit. People want to blame glucose and insulin, yet when you look at your blood, you see a loss of charge. Does Nature make mistakes, or has centralized medicine ignored many facts they should have been asking questions about? When deuterium is let into the matrix, this is what redox shifts all biochemical pathways the longevity experts THINK never change. Does this alter the charge, my dummies? This is why none of them understand how mTOR and UCP-2 work with 380nm light generated inside of us.

Those proteins embedded in the lipid rafts or connected to them by the tensegrity system change how they respond to charge and light. Why does NO fall as we age? Because modern humans live under an alien light. Why do APO proteins and LpA look like a problem to the Peter Attias of the world? Because none of his patients in NYC or San Diego live in sunlight. If they did, their LDL cholesterol would be low, and their HDL would be high, and he would not write a new book (@billgifford alert) telling everyone to take a statin because it is a GOOD plan for longevity. This message is DEAD WRONG. Send that to your dummy list on day three of Christmas! Stop making dummies popular and rich this Christmas!

B12 is a visual photoreceptor in humans. Bad blue light actually atrophies the CNS and PNS and makes your skin pale by degrading melanin. This is why MS and ALS are made worse by the blue light hazard.  The same thing is true for autism and brain gliomas.

Did you know B12 has another quantum function?  B12 limits the production of Nitric oxide in tissues.  It lowers the NO level to quench the effect of UVA sunlight.  What happens if you are vegan or vegetarian or a tech abuser and you do not have the right amount of B12?  It means your tissues won’t have the right amount of NO either.  UVA light heats tissues up, especially at the skin’s surface.  Did you know that heated-up skin and subcutaneous tissues make wake less likely to dissolve gases like NO, so they act longer on the tissue level to oxygenate them?  This is a reason people in the sun have higher tissue O2 levels.  It is why their blood has a higher venous saturation of oxygen, and it was the basis of how I realized my dying friend Jeremy Thomley was able to breathe through his skin by living on a Christmas tree farm in Hattiesburg, MS confounding all the centralized doctors at UAB medical center.

Without the right amount of NO, will your capillary beds be filled with the right amount of blood for that tissue?  Nope.  Might that cause hypoxia and lower other batteries, capacitors, or charge density carriers in your cells to lead to disease?  YEP.

Cobalamins also affects another battery that holds electromagnetic charge called the MTHFR system.  Methionine is part of the story you will learn about on the 11th day of Christmas below.

Blue light & nnEMF are net catabolic for your tissues, all loaded with several non-visual photoreceptors; moreover,  light radiation destroys them.  If melanin is not present, the destruction is even more rapid.  Why?  Melanin protects us from stray electromagnetic radiation.   Could mixing EMF with a Big Pharma toxin lead to a rapid death because of these lessons?  What did I tell people in LA in 2015?

There are a lot of Dummies who need this wisdom.  I made all these predictions way before COVID hit.  You can see the effect of vaccines when they are mixed with nnEMF because all vaccines are mitochondrial toxins.  And mitochondrial toxins ruin our tans outside and inside of our bodies.  This leads to a discharged battery and disease.  If your batteries already suck because you live in a city with 14 million other dummies, you can die fast from a flu shot.

WHAT IS THE NUMBER ONE nnEMF AFFLICTING HUMANS TODAY?

Blue light is.

This is why Anjan Katta’s new daylight computer is critical to buy for the dummies on your Dummy list. It is anabolic for the brain.  It stops human brain breakdown. The rhythm or color palate used in nature can be found in a molecule’s absorption and emission spectra.  I told Ray Peat this over a decade ago, and he ignored it at his tribe’s peril.  You should not, or you too will wind up a smoothed-brained Peatatarian.  I lit many of them on fire in August of 2023.  You might hear something about that in March of 2024.  The only supplement for my tribe is FSS.  See the cites below.

On the seventh day of Christmas, Uncle Jack said to me, why do I need Anjan Katta’s Daylight Computer? The answer is in his screen tech design. Wake up and go in the sun with it, and you’ll alter your charge like Nature built ya’. This is Christmas for Dummies Day! It’s a gift for people who thought they had everything and don’t. If someone had bought this for Steve Jobs, he’d likely still be alive. It is the gift of time given to your dummy list.

Start with every parent who babysits their kids with a phone or an iPad. There are at least half a billion of those dummies in your continent.

8. On the eighth day of Christmas, I hope some of you gift the Patreon wisdom to 5 dummies on your list. Or the smart dummies on your list, just pay five bucks a month for my Patreon insight and give them the gift of good thinking.  I promise to add charge density to the life for five bucks a month or 60 bucks a year.  You can join them up here at patreon.com/DrJackKruse

To get them addicted to decentralized thinking, give them this sample appetizer I made for this list on day eight.  https://threadreaderapp.com/thread/1735132650464051530.html

It will teach them to use time wisely.

Do you use time wisely? Do you prioritize your choices by weighing the value of information and wisdom against the cost of choice and decision?   Life is always wrapped in opportunity cost.   Decentralized medicine is both science and art in a unique package blended by perspectives of how the world is affected by Nature. Looked at from this vantage point, a good decentralized artist knows he has less time than ideas, and this pushes him to act, create, and share the ideas born in his craft. Time is too precious to waste.   The job of Nature is always to deepen the mystery for the artist. The artist’s job is to find the inspiration of Nature and reflect it in your creation and wisdom.

9. On the 9th day of Christmas, some reality comes to the tribe.  Increasing your charge density comes with a cost in a tissue.  This is why Nature compartmentalized its mitochondria in tissues.  Not all tissues have the same redox capability.  The brain and heart have the most.  The bone and immune systems have the next most.  This is why Sodium & potassium concentration is so critical in certain tissues and not in others.  K+ in the endolymphatic sac.  Sodium in the brain and Calcium in the heart are key examples.  The amount of UV light absorption correlates with this charging ability.  I taught the world that in the Vermont 2018 talk.  You can find that talk and the slide here on Patreon as an ala carte purchase.

With respect to the density of the electrolyte in a battery, If a high-density electrolyte is put in a battery, the capacity will increase to a certain extent. However, increasing density also means that the battery life is shorter.  That means redox collapse can happen.  Uncle Jack, can you give us an example?

Let us discuss the skin.  When you get overexposure to the skin and exceed your charge density capability, the sign that it happens is that you will itch in your skin, and your melanin upregulation will be slowed.  A sunburn should not itch as it develops.  If it does, it is evidence of a topological change in the skin.  We see this in many cases of atopy, dermatitis, mast cell dysregulation, lupus hypersensitivity, solar hypersensitivity, etc. Many drugs do this.

Phenothiazines, methylene blue, antihistamines, and many diabetes meds like sulfonylureas.  Sulfated antibiotics do it, as do all the floxin antibiotic drugs.   The biggest offender is birth control pills and NSAIDs.  Drugs are used to treat psoriasis, and many skin disorders do it.  What are the implications of this day 9 lesson on “charging?”  All of these drugs DEGRADE melanin everywhere.  They are not part of a melanin renovation program.  The Dummy list will get the post in this series.

If you do not know how to use MB, you can harm yourself.  MB increases NO delivery to tissues, and if you do that too long, you ruin the charge density of the tissue.  I have an older member on my forum who believes everyone should be on Nitric oxide because he listens to NO videos from people who don’t have a full view of the process, and I have to delete most of his threads.  Sometimes, members have to be taught lessons, too.  If they don’t like it they can exit.  I have taught all these things about NO to my tribe.  Now you know why I have to protect my tribe sometimes from overzealous members who lack comprehension of what I have written.  Never forget that NO is a free radical and must be quantized properly to marry tissue charge density.  Just because you’re old is no reason to pop NO daily.

The analogy to land this punch:  before you can eat the juicy fruit of health, you have to understand the destructive existence a seed goes through on the way to growing the tree in sunlight to create fruit photosynthetically.

How did I learn about battery life and charge density decades years ago?  As a neurosurgeon, patients with Parkinson’s disease who used a lot of L-Dopa before surgery always were deathly pale.  So, I asked my mentors about this situation.  The answer I got from our Medtronic rep on the early DBS stimulation trial data was instructive to my ignorance.

In cardiac pacemakers and DBS patients, manufacturers found that patients on certain drugs have poor battery performance of their implants, and this could lead to increased symptoms.  It turns out battery estimations, charge density, total power, and clinical symptoms were important to follow in patients with these devices. The observation of clinical worsening that was rescued following neurostimulator replacement only reinforced the notion that changes in clinical symptoms can be associated with battery drain.  This was one of my early introductions to physics in neurosurgery.  I found that in PD patients with poor battery life they often had co-morbid thyroid problems while being pale, and many were often on thyroid medication replacements.  It turns out low thyroid function also ruins battery function because it means melanin cannot do its job in the brain stem.  Why?

Melanin loses its electrical conductivity as heat is lost. So, more battery power is used in these patients to generate the DC electric current where melanin is missing in the brain.  Melanin electrical conductance is better when patients can maintain their own endogenous temperatures.  I did not know this as a young surgeon.  I began to realize why people who flew more got more blood clots.  The zeta potential in their blood was getting zapped by the solar wind and by a lack of grounding = fewer electrons in the blood.

Yes, RBCs are a type of battery that holds a charge, too, because they are loaded with another heme-based non-visual photoreceptor called hemoglobin, an iron porphyrin.

When I learned about this, I asked more questions.  I found that PD patients lost temperature regulatory abilities as they got worse.  They all had excessive sweating like diabetics do.  As they lost water and became dehydrated, they lost the ability to make Vitamin D, and they all became pale because they could not make melanin.  I then found out that altered NO levels were related to developing type 1 diabetes.  Most of them suffered from chronic hypoxia at the cellular level.

Many papers felt this was protective of lowering ROS signaling to prevent damage, but I found out in 2013 that pseudohypoxia drives NAD+ to low levels and is associated with more rapid aging of tissues.  I also found out that NAD+ recycling controls the circadian mechanisms in humans, and when NAD+ levels drop, you can bet there is ongoing melanin destruction in the brainstem of PD patients.

NAD+ is the link between the sun and HIF1, and taking exogenous NAD+ supplements down-regulates NAD/NADH function and physiology.  NAD+ only carries 2 electrons, while melanin creates 4 electrons from the charge separation of water.  If melanin is being degraded simultaneously as NAD+, you can see a serious lack of electrons in the system.  Melanin, not NAD+, is more critical in health and longevity.  See Rabinowitz’s papers in the Journal Nature for proof of concept.  If there is a lack of electrons in tissues, light cannot be utilized properly to make energy in humans.  All of these things made me realize this is why people with hypothyroidism, diabetes, and PD all carry high risks of developing melanoma compared to other patients.  It is a “charge density” loss in the skin story.

10.  On the tenth day of Christmas, my true love said to me…….get all the dummies OFF any and all NAD+/NADH supplements once and for all. Why?

Information transfer costs us energy = heteroplasmy is built in.   Landauer predicted that erasing even one bit of information would release a tiny amount of heat, a figure that he calculated. This implies mitochondria are time machines because they also transform light energy into CO2, water, and heat = mtDNA is a hydrogen heat engine.  If information is energy, as Wheeler has told us, Information, once created, has to have a “finite and quantifiable mass.”  This connects information theory directly to energy and mass equivalence. E-mc^2.  This is how they are linked.  Where is the link in biology?  NAD+ links to the heat shock proteins like HIF1.  Sinclair’s 2013 paper missed the real point of why pseudohypoxia aging and NAD+ dropping are linked.    Broken circadian clocks are 100% due to lack of sunlight or too much light at night = “charge” density story is missed.

NAD/NADH drugs are just slick marketing bullshit.    How do cells do it? Your epigenetic mutation load (EML) of your tissues is the key to understanding how the light you use in your environment builds the life you live.  Nature has built a clock timing mechanism as you live a life based on your light choices. A higher EML has been associated with age-related pathological conditions like X chromosome activation skewing.  What is X-linked chromosome activation skewing?

X-inactivation is a well-established dosage compensation mechanism ensuring that X-chromosomal genes are expressed at comparable levels in males and females.  Remember, males and females have different mtDNA inheritance, so there has to be a compensation mechanism for energy balance.

The higher latitude or, the more tech abuse you live with implies a lack of melanin.  As such, you have a higher risk of X-linked activation skewing in tissues with redox problems.  This sets the table for lots of problems in the sexes.  It might also be the smoking gun for childhood cancers.  If your kids have cancer, I usually ask my female farm members to get X-linked activation testing done.  Most are surprised until I explain why.  Think of your child as a battery.  You are designed by nature to transfer the surface charge in your tissues to your child.  You transfer more of it than your spouse because we inherit most of our mitochondria from mom. Yes, ladies, there are papers. Dad can do it, too, but it is not common.

Inactivation of the X chromosome may indicate a putative tumor suppressor gene on the X chromosome and the combination of a germline mutation of this gene and nonrandom X-chromosome inactivation.  Because leptin controls this process, these circumstances are more likely to be associated with a circadian mismatch in mammals.  This situation allows for the elimination of the wild-type activity of the tumor suppressor gene, and this results in an elevated risk of developing cancer in these females and in their kids.  Your kid is like a battery of your cells.  Imagine that.

For ladies, this, I believe, is why the BRCA1 gene can be a problem even when you do not have the classic inheritance.  Ladies with BRCA1 always have high-latitude lifestyles and are tech-addicted (think Angelina Jolie); skewed X-chromosome inactivation can arise independently but can and would cause enhanced tumor susceptibility.  Last warning about altered charge density:  skewed inactivation can result in heterozygous females manifesting X-linked diseases that are usually seen only in males too.  I have seen several females with Duchene’s phenotype that their geneticist could not explain.  Skewed activation testing did.  Somatic tissue needs to be examined before declaring a sample “ clonal.”  Solid research work has revealed a strong link between pluripotency and XCR in placental mammals. When naive embryonic stem cells (ESCs) differentiate, random XCI is induced in mammals with placentae = YOU!.

The circadian clock in humans controls chromatin marking in humans (pic below). BMAL1 is a clock gene, and HSF1 is a HEAT shock protein.

In humans, 55–70% of the transcriptome is under circadian control in any given cell type. This is the basis for circadian control of major physiological processes, including immune functions and, most importantly for this investigation, cell proliferation, morphogenesis, and X chromosome inactivation.

Circadian clocks operate in most tissues at the single-cell level. These clocks are based on clock genes at the molecular level, which participate in auto-regulatory feedback loops. In the core loop, the transcription factors CLOCK and BMAL1 activate the expression of Per and Cry genes, whose protein products negatively feedback on their own expression.

Dosage compensation between XX female and XY male cells is achieved by X chromosome inactivation (XCI) in mammals. XCI is initiated early during development in female cells and is subsequently stably maintained in most female somatic cells. What maintains it?  CIRCADIAN CLOCK MANAGEMENT!  Despite its stability, the robust transcriptional silencing of XCI is reversible in the embryo and in several reprogramming settings.

Examine the picture closely because it is decentralized science-dense.  Mouse and humans are mammals.  One is nocturnal, and one is diurnal.  XCI during female mouse and human development shows us how this works. During mouse development, embryonic cells around the 4-cell stage inactivate the paternally inherited X chromosome. Cells of the primitive endoderm and trophectoderm in the preimplantation blastocyst keep this inactivation pattern, while those in the epiblast reactivate the paternal Xi. Around implantation in the uterus controlled by leptin-melanocortin pathways, an X chromosome is randomly inactivated within epiblast cells. What if melanin is not there? What if leptin is not optimized?

Following the specification of PGCs, these cells activate the Xi. Primary oocytes within the fetus and adult mouse do not contain an Xi, while all somatic cells retain the Xi pattern of their epiblast precursor. During human development, random XCI is seen as a gradual process beginning in the early blastocyst and completing just prior to implantation; this pattern of inactivation is retained in all future somatic cells. Following the specification of PGCs, these cells reactivate the Xi, which remains active in all future germ cells.  Do you think melanin might affect this system with its ability to increase CHARGE DENSITY in cells?  Read on.  This list is for the Dummies in our lives.

Cells are colored by their lineage displayed in the upper right panel; primary oocytes (green) within the fetus and adults represent the primary oocytes contained in the ovaries of born offspring. The picture above does not accurately represent relative mouse and human development times, but you should get the gist. What does all the abbreviations mean?  PGCs, primordial germ cells; Xa, active X chromosome; Xi, inactive X chromosome; Xip, inactive paternally inherited X chromosome. Reproduced and adapted with permission from Pasque and Plath (2015).

Nature needs that to adapt to changing light and temperature in the environment, which is why those are the TWO METRICS the SCN pays attention to.  “Charge density” is the key to the periodicity of molecular clocks!

This is why all this stuff is linked.  STACK THE LESSONS IN THIS BLOG FOLKS.  I am giving you bombs here for Christmas to smarten up the Dummies in your life.  When leptin-melanocortin signaling is lost, NAD+ drops, and that tissue is aging faster on a relative basis than it should.  Aging is a loss of charge density when you have this perspective.  A healthy cell phone can hold a charge after you plug it in.  During sleep, we recharge and go back to the default state.  When NAD+ is low, or melanin is absent, you cannot recharge the battery no matter what.  Examples:  chordomas, fibromyalgia, Lyme disease, melasma, Hashimotos, ME, and soft tissue sarcomas.

11. On the eleventh day of Christmas, my true loves said to me……What about the viruses or jabs?  What if I told you that outbreaks of chicken pox, Shingles, and the herpes virus only come out when you lose charge density in a tissue?  Might that be related to a lack of melanin or lack of NAD+ in tissues?  YEP.

What if I told you that there is a way to repair any neurological disease by improving the mitochondrial redox power of your eyes and skin via the sun to import melanin through your blood-brain barrier without any help from Big Pharma? Would you believe me?

In 2014, bacterial melanin was proven to stimulate regeneration after mammal CNS lesions.  Imagine that.

Uncle Jack, is there anything else we should wise up about on the 11th day of Christmas?  You remember your mitochondria have a bacterial origin, right?

Did you know that your mitochondria can tan your guts and insides by using their bacterial-based mitochondria as a point source of light and a novel non-visual photoreceptor called melanogenin?  Yes, that is not a misprint.  I said exactly what you read and heard in your brain.  Do you believe me?

In 2005, this paper was written.  How come your experts did not tell you about it?  Melanogenin was discovered in NYC 15 years after leptin was.  Amazing how this research stayed hidden all these years.

Do you want to guess this biomolecule’s absorption and emission spectra, or should we save that little treat for another day?  It is in the visible range of sunlight.  I had to tell you!

Is there a missed charge density story that could explain myocarditis from the mRNA jabs linked to the wisdom on the 11th day of Christmas?  If you are vaccinated and a highly paid professional athlete, you should be screened for the SCN5A polymorphism and Bruguda syndrome.   Why would a P450 SNP be linked to this story?  All P450 SNP are cytochrome and subject to the destruction by blue light, silly!  See the picture below on line 1.  The P450 system is all heme-based biomolecules.

Four known common polymorphisms of the SCN5A gene are related to BrS, including R34C, H558R, S1103Y, and R1193Q. We always suggested this hack to my professional athlete clients who were forced to get the jab.  The Rx for it was “endogenous and exogenous melanin renovation therapies” done in the offseason to prevent some of the things you saw last NFL season.  If you are a vaccinated human with heart rhythm abnormalities, you should ask your cardiologist to screen you, too, even if you are not a million-dollar athlete.  Most centralized cardiologists have yet to learn about this decentralized wisdom.  In 28 NFL cities, I have asked many of them about this science and got blank looks.  That explains this—> JJ Watt and Hamlin both had heart issues after the mandated vax by the NFL.

These SCN5A polymorphisms often decrease the expression of sodium‐channel proteins and alter gating properties, resulting in prolongation of the QRS duration and slow conduction in the heart, making sudden cardiac death and rhythm changes more common in the face of mRNA damage = higher cardiac heteroplasmy in young people = unexpected morbidity and mortality.

I wrote about it here last year after the Buffalo/Cincy episode.   If you have the defect, you better avoid nnEMF too.  nnEMF causes C terminus problems = MTHFR.  You need this system to recycle methionine in your cells.  Remember the methionine and tryptophan blogs on Patreon?

You also MIGHT have a charge density problem if you have an MTHFR SNP that goes awry.  Do you know that COVID-19 and LONG-COVID patients suffer from this effect?  At the beginning of the pandemic, I was seeing so many people who were fit yet developed rapid onset diabetes.  In fact, I just got interviewed by someone in LA about this topic who it happened to.  I do not think she, her family, or her fancy rich doctors in LA know what I will tell you.

When I was in LA meeting with Rick and Bobby Kennedy Jr, I met three people with pancreatic cancer and sudden onset diabetes after COVID and their jabs.  The pic above and below show you why they got it.  How much do you know about methylglyoxal (MGO) for short?

Right about now, my driver in LA, Dan, is probably reading this and thinking about all the Dummies out there in LA-La land he met who need this information but just could not fathom I was right about what I told them.  Right now, Dan probably knows why I was so pissed at a breakfast we had when the discussion went from gold course to LA’s nnEMF burden and why that is such a problem for diabetes and tumors of the pancreas and brain.  Did you know excessive methylation, a C terminus issue, causes cancers by altering methylation?   I just wrote you a C terminus blog!

One of the staples of my LONG COVID Rx I use for my farm clients is MGO inhibitors.  I doubt you’ve heard of them.  Some of my therapeutic approaches with my tribe who got COVID because they REFUSED TO MOVE include (1) MGO scavengers such as aminoguanidine, alagebrium, and pyridoxamine; (2) MGO synthesis inhibitors such as metformin and benfotiamine (thiamine); and (3) Glyoxalase 1 inducer, via activation of the Nrf2, such as phenethyl isothiocyanate and selenium sulforaphanes.  (4) I use special concoctions of IVFs (below) to help change the surface charge of cells damaged by COVID-19 and/or the jabs.  Each jab and COVID variant has its own particular fluid I use.  It is 100% based on the charge these things impart to tissues.  We do the same thing in heart and kidney failure cases with low Vitamin D proxies, but few people understand decentralized thinking.

These folks have kept me busy.  I have had to turn away many people who only want to give 10% when they demand 100% of me because I no longer have time for people who refuse to do what I ask of them.   That is not how decentralized medicine operates.

LONG COVID-19 FOLKS NEED A TON OF SUN BECAUSE OF PEGYLATION

DMG-PEG 2000 is a synthetic lipid formed by the PEGylation of myristoyl diglyceride. It is used to manufacture lipid nanoparticles that are used in mRNA vaccines.  Why is it used?  It improves the shelf of the jab by hiding it from your immune system cells.  This comes with trade-offs.

All the cells in the blood become PEGGED with LNPs to alter their zeta potential.  Think about PEGylation like a magnetic force field around every biomolecule in your blood.  It ruins the electromagnetic signals normally present.  See my slide below from Vermont 2018.  This slide below is why I could easily understand the problem with the jabs.  The PEGylation changed the electromagnetic footprint in the blood that the sun is built to control.

The electromagnetic shielding from pegylation would form a protein corona around things in the blood like immunoglobulins or albumin. It would also inhibit it from binding to platelet factor 4, altering normal clot time!  Yes, clotting is controlled by the sun’s light, too.  The alteration of the zeta potential is an electromagnetic change.  As you can see from the picture above, the zeta potential of all Pegged things interacts with their surroundings. When it does, forces are generated that are not quantized properly, and viscosity changes, and so does flow.  When the zeta force is strong, we know too much highly negative charge density exists.  This could be high nitric oxide or way too many electrons.  When this happens, blood cells will act to repel objects with like charge and keep them at a distance.

Big Pharma has figured out how to navigate the circulatory system to get into every organ system using the surface charge variation of drugs.  Pegylation is just one way.  Pharma scientists can customize any cell’s zeta potential based on the specific route they want to take in the body via the blood. Ralph Baric et al. and his friends in the DoD built spike proteins with a zeta potential to interact with human endothelium and the heart.  This is why so many young people get myocarditis and clots.  The science is so advanced now that they have learned how to control pegylation effects remotely with RF radiation.  This operates just like your TV remote control.  They learned this from CORONA virus gain of function research.  It is called the “corona” virus because its activity varies with the zeta potential changes found in seasonal sunlight.  In nature things in the blood are quantized by sunlight.  In long covid, your decentralized doctor must figure out the charge density variations to come up with the right Rx for you.  No one Rx fits everyone.  This is why protocol medicine fails.  It is also why I am not advocating McCoullough’s protocol.

What could make a cytochrome go awry in a big American city with a ton of people abusing nnEMF? Did you know the MTHFR photoreceptor system is how evolution built us to survive winter when glucose is rare?  It allows our immune system to work even when the sun is not shining.  MTHFR is a capacitor for electromagnetic energy.  Capacitors hold charges.  Melanin and water are charge capacitors.  So is MTHFR.  Can you imagine the effect of all this and then adding some DNA plasmids and SV 40 to the mix?  What do you think might happen to people in that risk strata?  Does Nature have a hack for people with long-term COVID-19?   Staying immune through the fall & winter and a city with nnEMF is a quantum mechanical human longevity trick.  It’s a good thing I stopped being a dummy 20 years ago.

Every week, I put out a new podcast on how energy is transformed by the aging silly talking clade of primates called humans. Physics tells us energy cannot be created or destroyed; it is just transformed in cells.  Rarely do biochemistry books get the story correct.  Physics tells us time is relative, and how we experience it is tied to tissue-level entropy.  Tissue level entropy is called heteroplasmy by mitochondrial experts. The lesson?

Blue light stimulates insulin and blood glucose.  This means ALAN never allows us to create glucose from our fatty acids.  So, biochemistry books were written after 1951, and all said that it is impossible to create glucose from them.  Is this another reason why blue light and nnEMF help make us fat?  We never recycle our adipocytes, and they remain filled?

Let’s talk about winter.  What happens when insulin levels fall, and ketone levels rise, as occurs when our carbohydrate intake is low, is our cells increase their supply of CYP2E1 and thereby activate the conversion of fatty acids to glucose.  It appears the books were wrong, and Mother Nature found a way to a costly candy store in the magical land of ketogenesis when it is cold and the sun is not strong.  What happens when melanin is absent from mammals?

When I was in medical school in the 1980s, two reviews were published outlining the evidence for converting fatty acids to glucose.  One of them dated to the early 1950s.  One of them emphasized that biochemistry students were taught that such pathways do not exist.  The same Ph.D.  (Peter Setlow at UCONN) who warned that the cholesterol story was BS, told me that we could make glucose from fatty acids because mammals like cows, guinea pigs, mice, and rats all turn acetone into glucose if they have to.  He told us that this is why some diabetics have acetone breath odors.  He told us the same thing about chronic alcoholics.  This explained to me that alcohol was not a longevity toxin if you lived in the sun and why Jean Calment could live to 122.4 years old drinking red wine every day in the south of France.  This lesson taught me never to trust textbooks.  You have to read the PublMed papers to see the real truth.  Centralized academics just regurgitate bullshit beliefs they hold as truths.

The most cost-efficient way of converting fatty acids to glucose is by converting acetol to methylglyoxal, facilitated by an SNP called CYP2E1.  CYP2E1 is a P450 cytochrome.  Did you know that the cytochrome P450 system is a heme-based semiconductive system that is part of the non-visual photoreceptor system mentioned above?  CYP2E1 is involved in acetone catabolism by converting acetone to acetol and then to methylglyoxal (MGO); both intermediates in the gluconeogenic pathway.  These metabolites are prominent in the brains of mammals where mitochondria reign.  This P450 enzyme also catabolizes safely exogenous compounds such as inhalational anesthetics, ethanol, nicotine, acetaminophen, acetone, chloroform, chlorzoxazone, and tetrachloride.  It is also important in the melanin renovation Rx because it removes aspartame.  Aspartame lowers melanin levels endogenously.  Excessive use of it leads to many problems in humans.  One problem is that all mammals become more sensitive to electromagnetic radiation when their tissues lack melanin. Another thing that happens is that mammals seem to get diabetes more easily than ever before.  Might it have something to do with melanin, NAD+, and the P450 system?  All those lessons are in this blog for the Dummies on your list.

12. On the twelfth day of Christmas, my true love gave to me…………a relationship filled with electrons.  Being with the right person is a net positive to your charge density.  I wrote an entire series on relationship redox on Patreon, so have your Dummy list read it.  So, if you think you are with the right person, ensure you get them everything on this list.  Make sure you kiss and love them and add electrons to their life.  Tell your honey how you feel about them today on the final day of Christmas.

You. You are a gift. It is a year-long Christmas gift, not a seasonal novelty with a shelf life. Your circle of six should always be proud of you and not jealous. They should build you up, not tear you down. They don’t give you a total pass all the time. They will keep you on your toes and prune your branches when needed. They love to see you win. Their wisdom is fertilizer for your growth and not criticism to stunt it. They certainly do not deserve your friendship and time if they cannot celebrate your success. Never forget how amazing some of us think you are every day. Write your story. I’m utterly convinced that our circle of six experiences is meant to support one another, and they are all relevant in some form or fashion. Every one of these experiences matters, and the Universe is so well-designed that we need these experiences to thrive. You are a gift to some of us, not all of us. Parcel your time wisely.

DUMMY SUMMARY

Instructions for Dummies have to be explicit, or they lose the plot. Retweeting without reading is not capturing wisdom.  It just gets you an army of dummies.

Surface charge  = topological change. Therefore, surface charge changes are the starting point for most adverse events in disease.

How do we determine the surface charge of anything?  The surface charge can have either a negative or positive electrical state. It is determined by the balance of charges between negatively charged and positively charged nanoparticles at the surface. The cell membrane surface of living cells has an electric potential different from that of the cell’s interior, namely membrane potential.

For example, here is a study on inhaled LNPs with a POSITIVE ZETA POTENTIAL OF 42! This tells you there are a lot of protons in this LNP.

It should be clear for those who are actually reading my Patreon blogs or tweets and learning the lesson.  What do you think might happen when you introduce an LNP with a large positive charge  (zeta potential big) to the lungs? ANSWER:  That is how you get a pulmonary embolus or MASSIVE THROMBOSIS in an arterial bed.

A strong increase in the surface energy is obtained when the size of the lipid nanoparticle decreases, both in the solid and liquid states.

The latest results show that the nanofluids’ surface tension increases with concentration and nanoparticle sizes. TiO2-DW nanofluids exhibit higher surface tension than Al2O3-DW and SiO2-DW nanofluids, respectively.  Yes, Titanium dioxide in your foods and cheese as a lot in common with pegylation in the mRNA jabs.

If you are not reading, you are not learning my work, much less understanding it.  You are a dummy, and this list is for you.  —->  https://openres.ersjournals.com/content/5/2/00161-2018

Thermodynamics is defined by energy and charge.  Size and shape changes alter charges, and the zeta potential is how this is measured in blood. In a tissue or biomolecular real or manufactured, when we hold a constant pH and salt concentration, the magnitude of surface charge decreases with an increase in the particle size and reaches a constant when the particle size exceeds a critical value.  This is why lipid biochemistry is a joke as a risk factor for heart disease.  Calcium Index scoring is a way better marker for heart disease because it is a topological effect telling us that the circulatory system’s surface charge is abnormal.

·CITES

1. https://www.botianchemical.com/sale-14313842-high-purity-99-0-titanium-dioxide-anatase-food-grade.html

2. Yeah, the new DUMMY supplement called FSS = Full Spectrum Sunlight.

3. https://www.nature.com/articles/s41431-018-0291-3

4. Navarro, P.; Chambers, I.; Karwacki-Neisius, V.; Chureau, C.; Morey, C.; Rougeulle, C.; Avner, P. Molecular Coupling of Xist Regulation and Pluripotency. Science (80-) 2008, 321, 1693–1695.

5.  Escamilla-Del-Arenal, M.; Da Rocha, S.T.; Heard, E. Evolutionary diversity and developmental regulation of X-chromosome inactivation. Hum. Genet. 2011, 130, 307–327.

6.  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005010/

7. https://www.europeanreview.org/wp/wp-content/uploads/8152-8171-1.pdf

8. https://chrismasterjohnphd.substack.com/p/we-really-can-make-glucose-from-fatty

9. https://www.sciencedirect.com/science/article/pii/S2052297523001075

QUANTUM ENGINEERING #64: LIGHT IS INFORMATION

Many forget light is both a particle and wave.  It has a duality.  Life uses that advantage.  Light from the sun acts more like a wave than a particle and that is how we use it as ainformation.  Light created by photosynthesis (food) or by cells (bio-photons) acts more like a particle.  No one should forget both pathways LIGHT IS INFORMATION.  How it is used as information is what varies in Nature.  I covered that here.

INTRODUCTION

Do you use time wisely? Do you prioritize your choices by weighing the value of information and wisdom against the cost of choice and decision?

Life always is wrapped in opportunity cost.

Decentralized medicine is both science and art in a unique package blended by perspectives of how the world is affected by Nature. Looked at from this vantage point, a good decentralized artist knows he has less time than ideas and this pushes him to act, to create, and to share his ideas born in his craft. Time is too precious to waste.

The job of the Nature is to always deepen the mystery for the artist. The job of the artist is to find the inspiration of Nature and reflect it in your creation and wisdom.

Optical biophysics studies how light is transformed into information for cells.  Cells are filled with non-visual photoreceptors to capture the electromagnetic properties buried in photons of the cosmos.  Biology is not a foundational science. Physics is.  Optics forms the solid-state physics of the living state. This means paying attention to the light emissions and absorption frequencies from cells, DNA, and molecules of organic matter and how these interface with water.  At birth, we are 80% water; at age 60, we are at 55-60% water by weight.  Cells capture light and create water and are moderated by the nested array of electric and magnetic fields transformed by mitochondria located on the quantum level and capable of stretching up to the galactic level where plasma is ubiquitous. This plasma connects everything in an electrical circuit at unfathomable ranges and power.  We do not operate at all ranges of this spectrum.  This plasma has a pulse or rhythm to it.  Our cells pay attention to this music and to its rhythm.  The rhythm can be found in the absorbtion and emission spectra of a molecule.

Melatonin is a hormone that is naturally made by the mitochondria in your tissues, and its production is closely tied to light. In response to darkness, the mitochondria in our tissues initiates production of melatonin but light exposure at might or artificial light during the day slows or halts that production in mitochondria.  The pineal gland is not where the melatonin story begins on circadian clock maintence.

This is the range of nature’s music, which we are part of and can tune into. All parts of this spectrum have biological effects. Some are good, and some are harmful to cells.  This is the nature of light exogenous to our cells.

The organism creates its own music endogenously— of a somewhat more restricted but still enormous range between 10^-7 m and 10^8 and beyond — it is both exquisite and subtle. With the present level of ‘man-made’ electromagnetic pollution of the environment, one might very well ask whether the organism’s melody is in grave danger of being drowned out altogether by our mitochondria.

When we listen to a good talk, book, or podcast, whether off-the-cuff or seared into our memory by emotion, something in us is built to hear this music, not just in its register, the lilt, the cadence or its rhythm, but, in those moments, there are no words to be heard; all you can hear is the enveloping silence.

The same is true with cells…..the photons in the sun are sounds, while the silence is found in the darkness of night. The real music of life is found at night when light is absent. This is why ALAN, called artificial light at night, is so dangerous to humans.  Feedback coupling has many facades in reality, and few in centralized science realize it.

Melatonin is made in the morning and during the day, but it only acts to delocalize electrons under the cover of darkness.  Melatonin is like a conductor of Nature’s music.  Few understand how sunlight gives its information to serotonin to create melatonin in our mitochondria.  Sunlight transforms serotonin into melatonin and melatonin, then IMBIBES our cells with quantum information to ensure cells display significantly higher amounts of both p53 and acetylated p53.  This biochemical signal is the basis of the anticancer effect of mitochondrial melatonin.  This is how light becomes biochemical information.

Not to discount the bio-chemical nature of life, which is hegemonic in the health science realm, the optical bio-physician asks: which of these is PRIMARY in the growth, replication, and division of labor of individual cells or entire species of organisms? Is it the chemical attributes of living matter or the electromagnetic properties?

Mitochondria, the transformer of light to melatonin, are not mechanical machines; you should never think of them this way.

Mechanical systems work by centralized control. Centralization is a hierarchy of controllers and the control that returns the systems to set points (equilibrium). Life is never at equilibrium.  Mitochondria are fully built to be decentralized to light and dark cycles.

HOW DID WE COME TO KNOW THAT LIGHT IS INFORMATION AND BOTH LINK TO ENERGY?

Claude Shannon is regarded as the father of information theory. Alan Turing is known as the father of computer science. In 1943, Shannon and Turing worked on different projects at Bell Labs in New York City. 

In 1948, intersecting with Shannon’s pioneering theory on information, Alan Turing simultaneously wrote a report at the National Physical Laboratory on “Intelligent Machinery” that laid the groundwork for the emerging fields of information networks and artificial intelligence.

They had discussions together, including about Turing’s “Universal Machine,” a type of computational brain. Turing seemed quite surprised that in a sea of code and computers, Shannon envisioned the emergence of arts and culture as an integral part of the digital revolution – a digital mitochondria of sorts. What was dreamlike to Turing’s imagination in 1943 has become today’s reality.  Shannon’s early connections between the arts, information, entropy, and computing intuit the future we are experiencing today.  Turing famously said “Shannon wants to not just feed data to a brain, but cultural things! He wants to play music to it!”  Shannon knew there was art buried in the nature of information.  There was an inherent rhythm in both men’s ideas.

Order and chaos are deeply linked in nature by rhythms.  The paper above was the first paper that showed us how feedback loops could organize chaos in light & dark to build circadian biology using waves in rhythm.  It requires no complexity and is a feature of Nature’s self-organization ability.  All it requires is a feedback loop to operate.  Turing was the first to crack the key biological rhythms in life.

WHAT DID TURING STUMBLE INTO?

More light = more information in the system to build complexity.  Darkness makes the information durable and usable.  Energy tends to dissipate in the universe — and entropy, a measure of its dissipation, increases over time.

Time appears as entropy in cells and is coded for by molecular clocks.  All clocks are flow meters of entropy.  This is how matter organizes disorder into order. When a dissipative system controls entropy, life can manifest.  This is a very basic idea in quantum biology that Turning explored before quantum biology became a disciple of decentralized science.

Three years before Turing’s paper in 1951, Claude Shannon shook up the world with his work on information theory.

In 1948, Claude Shannon’s paper showed that entropy is linked to information. Entropy is a way to measure the amount of information in a source. The more information you have, the higher the entropy of the source is.  A high-entropy message means low information gain and a low-entropy message means high information gain. Biology wants to create a low entropy game in cells so cells can collect massive amounts of information.  Mother Nature built cells filled with clocks to take advantage of this idea.  Information gain can be thought of as the message fidelity in a system: the amount of clean knowledge available in a system.

To physicists John Wheeler, the ideas of Turing and Shannon implied energy and information are deeply linked. John Wheeler proved that was true in physics using the Landauer Principle (1961). Biologists still have no idea about the implications of this work.

Landauer’s principle is a physical principle pertaining to the lower theoretical limit of energy consumption of computation. It holds that an irreversible change in information stored in a computer, such as merging two computational paths, dissipates a minimum amount of heat to its surroundings. Landauer’s principle states that the minimum energy needed to erase one bit of information is proportional to the temperature at which the system is operating.

At room temperature, the Landauer limit represents an energy of approximately 0.018 eV (2.9×10^−21 J). Modern computers in 2023 use about a billion times as much energy per operation. This means information transfer in nature always has an energy cost. This is why nature uses a PoW mechanism. It explains why John Wheeler said information and energy are the same physical entity in Nature.  It might also explain why cells are filled with water to dissipate the effect of heat created during information processing.  Remember water has a massive heat capacity.

Wheeler divided his own life into three parts. The first part he called “Everything is Particles.” The second part was “Everything is Fields.” And the third part, which Wheeler considered the bedrock of his physical theory, he called “Everything is Information.”

When Shannon was at Bell Lab in 1948, Bell labs had tons of information buried in their messages but had no way to mine or collect the information to make the data useful. Shannon thought about the problem and wrote a paper about using mathematics to data-mine information.
The paper was called “A Mathematical Theory of Communication.”

Once Shannon connected these dots mathematically, it opened the door to signal processing, compression, and converting messages into an algorithm code to transmit them digitally. It gave rise to the Cambrian revolution in computers after 1948.  Turing died in 1951, but his ideas lived on in many computer engineers.

THE LINK TO ENERGY AND THERMODYNAMICS

Shannon’s limit in information transfer mathematically looks exactly like Boltzmann’s equation for entropy in thermodynamics. Entropy was an idea originated in the 1824 by Carnot.  I’ve written Patreon entries on Carnot’s theorem.  Both concepts, bit and photon, share the same roots: nineteenth-century thermodynamics and the concept of entropy.

 

In 1877, Boltzman gave us a statistical explanation of the second law of thermodynamics. In 1877, he provided the current definition of entropy. Shannon’s papers gave us a similar answer for information as his equation shows below.

Because these two equations are nearly identical mathematically, physicists began to realize in the 1960s that information and energy are linked physically in reality.  Nature is revealing her secrets in these equations.

Shannon’s work on information entropy links to Michael Crawford’s theory on DHA. These ideas coordinate with Einstein’s special relativity (1905). Einstein’s work directly ties to the Landauer Principle (1961) to explain how cells use light to communicate. Information transfer costs us energy.

Landauer predicted that erasing even one bit of information would release a tiny amount of heat, a figure that he calculated. This implies mitochondria are time machines because they also transform light energy into CO2, water, and heat = mtDNA is a hydrogen heat engine.

If information is energy, as Wheeler has told us, Information, once created, has to have a “finite and quantifiable mass.”

This connects information theory directly to energy and the mass equivalence equation of Einstein, E-mc^2.

This is how they are linked.  Light is light energy in photon form.

HOW DOES THERMODYNAMICS LINK TO THE CIRCADIAN CLOCK?

How do cells do it? Your epigenetic mutation load (EML) of your tissues is the key to understanding how the light you use in your environment builds the life you live.  Nature has built a clock timing mechanism as you live life based on your light choices. A higher EML has been associated with age-related pathological conditions like X chromosome activation skewing. The circadian clock in humans controls chromatin marking. BMAL1 is a clock gene, and HSF1 is a HEAT shock protein.

Remember what I said about Landauer’s principle above. As information is transfered, so is heat. This is why we have heat shock proteins in cells.  Both get optimized by sunlight exposure. HSF1 is an important transcription factor for the induction of NAT1 in human cells and is required for androgen activation of the NAT1 promoter. This is why Neil Armstrong had lifelong problems with his testosterone levels when he returned from the moon, and it is why so many women struggle with sex hormone problems in their lives when they are filled with methylation problems from alien light. This is how humans inactivate the X chromosome to limit disease and create time. If we choose badly, the opposite occurs.

Shannon realized that the quantity of the message had ZERO to do with its true meaning. No one yet realizes the same thing is true in humans in how their colony of mitochondria works with sunlight.
Shannon found just using a “one and zero” is all it took to solve Bell Labs’ problems around understanding information = where the word “bit” comes from.

Physicist John Wheeler gave us the idea that everything is information.” = it from bit……..
Wheeler tells us every particle in the universe emanates from the information locked inside it.

Mitochondria are Turing machines that use Shannon’s binary code of 0 and 1, where 0 = H+ and 1 = deuterium, and solar photons drive the Boolean logic gates in the mitochondria to action. Mother Nature-innovation was profound. She created an electromechanical switching circuit that could decide things. She proved 3.8 billion years before Shannon that it was possible to perform complex operations by means of electromagnetic relay circuits built from hydrogen isotopes.  I covered how mitochondria do this here ——-> https://optimalklubs.com/kruse-for-dummies-general/

NAD+/NADH is a proxy for melatonin production in our mitochondria by the rhythm and time of sunlight and by darkness in our lives we get.  Melatonin is the key light hormone that protects the heteroplasmy rate mitochondrial DNA to keep clocks operating well.  You won’t hear that from a food guru.   This means melatonin is the photochemical  gate keeper of the % of heteroplasmy in mitochondria in a cell. It not only controls inflammation (entropy) but it also controls turnover of DHA in the membranes of our cells.  This complex dance begins in the skin and eye, at the RPE, where ocular melanin and melatonin begins its quantum magic by using AM light to regenerate the melanopsin receptors in broad daylight by using UV and IR light.  They operate together when UV-IRA light are present simultaneously.

THE ANCIENTS KNEW ABOUT THIS LINKAGE

The roots of brain entrainment delve deep into history, where rhythmic stimuli like drumming or flickering flames were used in ancient rituals to induce altered states of consciousness. This primal concept has evolved into a sophisticated technology where light is the rhythm conductor for the brain’s symphony of mitochondria.

The spins of electrons/protons are not only manipulated by light. Light has both electric and magnetic fields. Spins of electrons and protons are also affected by magnetic fields (ATPase of mitochondria or the dynamo of Earth or those found in tech gear). It turns out spin states can also be affected by electrical fields (emitted from proteins side chains) and can be used to collect and store information optically from electrons or the photons they carry. This allows energy and information to be buried and included in the atomic structure of cells.

Brain entrainment through light pulsing hinges on synchronizing the brain’s electrical patterns with external stimuli. By emitting light at specific frequencies from mitochondrial metabolism, the brain is coaxed into a ‘frequency following response‘, aligning its brainwave patterns to the rhythm of the light.

This synchronization isn’t just fascinating; it’s profoundly useful from a physiological and evolutionary perspective.  Our brainwaves mirror our mental states – beta waves dominate when we’re focused, while alpha waves signify relaxation. By entraining these frequencies with light, we can potentially steer our mental state, precisely guiding the cognitive ship.

The cellular organization is the key to precision optical signaling. Life is all about optimizing optical physics inside cells. It transforms energy from the environment to do this. Modern physics has now proven that energy and information are equivalent in physics. Landauer & Shannon’s work was critical in making this linkage.

The cellular organization is the key to precision optical signaling. Life is all about optimizing atomic molecular organization (AMO physics) INSIDE OF CELLS. It transforms energy into information from the environment. Modern physics has now proven that energy and information are equivalent in physics. Landauer & Shannon’s work was critical in making this linkage. Modern quantum biology has experimentally proven that energy is trapped directly at the electronic level in cells. Energy is stored not only as vibrational and electronic bond energies in biochemicals but also in the structure of the system: its membranes, gradients, fields and flow patterns, compartments, organelles, cell water, the size and shape of our ventricles, and tissues. All this, in turn, enables organisms to mobilize their energies coherently at any time it is needed and hence make available the entire spectrum of stored energies for physiological work. Life really is energy transformed on demand by Nature’s atomic design in cells.  Light is the information powering the ENTIRE system.

SUMMARY

Who described the mathematics of decision-making?   Claude Shannon did.  Shannon showed how to map logic onto the physical world (ledger).  Turing showed how to design computers in the language of mathematical logic.

Mother Nature pre-dated both men’s ideas by 3.8 billion years.  Evolution was Nature’s laboratory that ended by creating a mitochondria which acts as a Turing machine.

Our brains need to optimally encode different options and compare between them. So, how did Nature build the brain?  It created an organ filled with mitochondria that responds at an attosecond level to electric and magnetic fields at 90 degrees to each other in light waves.  Our brain is measuring light waves to decipher the chaos in our environment.  In an abstract way, it mimics the double-slit experiment in physics.

With this brain, decision making became more probable.  During human decision-making, attention plays a pivotal role by guiding information sampling between alternative pathways in the brain’s mitochondria.

One of the hallmarks of the living system in cells is that they are exquisitely sensitive to specific, weak rhythmic signals.

During human decision-making, attention plays a pivotal role by guiding information sampling between alternative pathways in the brain. Our brains need to encode different options and compare them optimally using optics. So, how did Nature build the human brain?  It created an organ that responds at an attosecond level to electric and magnetic fields at 90 degrees to each other in light waves.  Our brain is measuring waves to decipher the chaos in our environment.  It mimics the double-slit experiment in physics.

So far, the role of attention in decision-making has only been addressed through saccadic displacements in our eyes.  Might saccade be the first clue that the brain is using our eyelids to episodically polarize unpolarized sunlight to create a new type of rhythm to make sense of our world?  This NEW idea implies that seeing is not always attending, and attending is not always seeing.

Brain entrainment with light pulsing is more than a biological evolutionary advance.  It might be the next frontier for neuroscientific technological advancement; it’s a window into peering into the vast potential of the human mind.

When Shannon met Turing

Computing fell in love
with digital information

A transformation
A revolution
New computations

Sparking innovations

When Shannon met Turing
a moment enduring
Alluring algorithms
touched information theorems

Analogue meets digital

Goodbye physical

Snapshots of the past

Silos can’t last

Connecting digital dots

Bits and bots

CITES

1. https://www.mdpi.com/1099-4300/19/7/341

2. https://pubmed.ncbi.nlm.nih.gov/24920214/

3. Glickson, J. (1986-87). Photic driving and altered states of consciousness. Imagination,

Cognition and Personality, 6, #2, 167-182.

4. Bergamini, D. (1965) Mathematics. Life Science Library, Time-Life International.

5. Blyth, T. (ed.) (2014) Information Age: Six networks that changed the world. Scala Arts & Heritage Publishers.

6. Bostrom, N. (2014) Superintelligence: Paths, Dangers, Strategies. Oxford University Press.

7. Bowen, J. P. (2012) Alan Turing. In A. Robinson (ed.), The Scientists: An Epic of Discovery. Thames and Hudson, pp. 270–275.

QUANTUM ENGINEERING #63: THE QUANTUM ATPase

Man is way behind Mother Nature.  Wolfgang Pauli realized that the free electrons in metal must obey the Fermi–Dirac statistics. Using this idea, he developed the theory of paramagnetism in 1926. Shortly after, Sommerfeld incorporated the Fermi–Dirac statistics into the free electron model and made it better to explain the heat capacity. Two years later, Bloch used quantum mechanics to describe the motion of an electron in a periodic lattice.

The mathematics of crystal structures developed by Auguste Bravais, Yevgraf Fyodorov, and others was used to classify crystals by their symmetry group, and tables of crystal structures were the basis for the International Tables of Crystallography series, first published in 1935.  The band structure calculations were first used in 1930 to predict the properties of new materials, and in 1947, John Bardeen, Walter Brattain, and William Shockley developed the first semiconductor-based transistor, heralding a revolution in electronics.

Why did Nature innovate chlorophyll and hemoglobin before moving on to melanin in the evolutionary history of mammals?  She learned that nitrogen and hydrogen could be liquefied under the right conditions and would then behave as metals.  Then she had some solid-state physics she could innovate life with.  Nature innovated the idea that a classical electron can move freely through a metallic solid in an aqueous liquid crystal.  She realized the power embedded in anisotropic crystals, built us from them, and self-assembled them in sunlight’s electric and magnetic fields.

Birefringence is the optical property of a material with a refractive index that depends on light’s polarization and propagation direction. Birefringence occurs in anisotropic materials that are said to be birefringent.  Piezoelectric materials, like bone or collagen,, are anisotropic; they do not have the same properties in all axes. 

Is the ATPase ANISOTRPIC?

What do you know about phosphoresce and ATP?  Is this important in creating the spectrum of biophotons from mitochondrial metabolism?  Is this how it can vary?  The answer is yes.  Metabolism makes heat, light, CO2, and water.  You do not see the light because mitochondrial matrix-created water is an electromagnetic capacitor for these bio-photons.  The water is structured in coherent domains to be transformed for physiologically useful energy in a cell.  This is the PoW mechanism at the core of the quantum cell.

In simple terms, phosphorescence is a process in which energy absorbed by a substance is released relatively slowly in the form of light. This is, in some cases, the mechanism used for glow-in-the-dark materials, which are “charged” by exposure to light.

Do you know that outside of the visible light spectrum, nnEMF causes calcium efflux?  What is the effect of calcium efflux on the ATPase?

Did you know that the presence of excess calcium ions has been found to cause a 20% decrease in the phosphorescence emission anisotropy in a cell?

In centralized science, this is interpreted as being due to a conformational change in the protein based on the methodologies being studied.  Moreover, it is supported by data from time-resolved phosphorescence measurements.  These measurements also show a hard physical effect of nnEMF:  nnEMF toxicity lowers the anisotropy.

Anisotropy is a basic property of all crystalline materials. Living tissue is anisotropic.  The organism is a dynamic liquid crystalline continuum with coherent motions on every scale.
Even in nanocrystals and amorphous solids, e.g., metallic glasses, anisotropy is present on an atomic level. Therefore, magnetic anisotropy is an intrinsic property of magnetization in general.

For nanoparticles that are used in the quantum cellular design, this is hard to achieve: because of their small size, they are generally only slightly polarizable by light, and thus, the difference in potential energy will, for accessible electric fields, below. This implies that the conditions for alignment are specific and sensitive to electric fields in cells.  Physics has shown that the minimum size to align a particle depends on the size and shape of the particle because of a nontrivial competition between particle bulkiness and anisotropy.

Anisotropy, denoted by lowercase “r” in physics equations, indicates molecular size, diffusion, and viscosity.

Several physical techniques or forces in nature can be employed to assist the self-assembly process in cells, such as alignment of the particles by introducing a substrate to the system (atoms), employing a fluid flow (viscosity), or applying external magnetic (free radicals) or electric fields (Becker’s DC). An external electric field can align an anisotropic particle due to its anisotropic polarizability, which causes the particle’s potential energy to vary with its orientation in the field present in cells.  nnEMF changes this thermodynamic variable.

Since the thermal Brownian motion (Einstein’s most cited 1905 paper) competes with the tendency to align, the potential energy difference has to be high enough to overcome these fluctuations and substantially align the particle.

The dependence of the minimum size of an alignable particle on the shape ratio of the particle is non-trivial, as it is not in general true that for alignment, the more anisotropic the particle, the better, nor are bulkier particles always better: for all the particle shapes studied so far, the optimum shape lies in-between these variables.  This implies abnormal Calcium movements in mitochondria have huge anisotropic effects in mitochondria.  This larvae shows that effect below.

This change in the decay of the emission anisotropy is associated with only minor changes in the rotational relaxation time of the protein and is again suggestive of a conformational change in the protein. This means that one of the biological effects of nnEMF is an altered conformational change in protein semiconductors.

For example, muscle contractions reduce anisotropy; for instance, contraction of the quadriceps muscle can decrease anisotropy of the patellar tendon.  If that muscle contraction is done under blue light, it compounds the effect inside of mitochondria.

In the brain anisotropy can be seen on MRI.  Anisotropy measures describe the directional dominance of water diffusion within a region. Within a voxel, the anisotropy provides an index of the degree of uniformity of water diffusion for a specific orientation. Strongly directionally organized tissue, such as the corpus callosum, which is primarily comprised of tightly packed medial–lateral projecting fibers, has a high degree of anisotropy because there is a tendency for diffusion to be highly restricted along the fiber membranes to follow this medial–lateral direction.

However, when the callosal fibers intersect other pathways in the brain, such as the corticospinal tracts which control motor movement, this unidirectional organization is disrupted and the anisotropy is reduced. This has implications in diseases like ALS, Parkinson’s disease, and Alzheimer’s disease.  Thus, there is a normal anatomy of the cerebral white matter of both high and low regions of anisotropy, and it is therefore not the case that greater anisotropy is always indicative of greater tissue integrity in human brain MRI. In fact, measurements of anisotropy have been performed for various brain diseases, and abnormalities (mostly reduction) have been reported.

In strokes of the human brain, diffusion tensor imaging shows an
increase in fractional anisotropy because of changes in the ATPase and mitochondrial response to hypoxia.

Welding fumes contain several metals, including manganese (Mn), iron (Fe), and copper (Cu) that at high exposure, may co-influence welding-related neurotoxicity. The relationship between brain accumulation of these metals and neuropathology, especially in welders with subclinical exposure levels, when compared with controls, welders had significantly lower fractional anisotropy in the globus pallidus where Parkinson’s Disease occurs.

SUMMARY

It was Albert Einstein who created the modern field of condensed matter physics, starting with his seminal 1905 article on the photoelectric effect and photoluminescence, which opened the fields of photoelectron spectroscopy and photoluminescence spectroscopy, and later his 1907 article on the specific heat of solids which introduced, for the first time, the effect of lattice vibrations on the thermodynamic properties of crystals, in particular the specific heat.

Condensed matter physics is the field of physics that deals with the macroscopic and microscopic physical properties of matter, especially the solid and liquid phases, which arise from electromagnetic forces between atoms and electrons. This field concerns itself with soft matter.  This is the matter cells are made from.

Condensed matter physicists seek to understand the behavior of these phases by experiments to measure various material properties and by applying the physical laws of quantum mechanics, electromagnetism, statistical mechanics, and other physics theories to develop mathematical models and predict the properties of extremely large groups of atoms.

Anisotropy is firmly in the scientific realm of the condensed matter physicists.  The diversity of systems and phenomena available for study makes condensed matter physics the most active field of contemporary centralized physics: one-third of all American physicists self-identify as condensed matter physicists.

Anisotropy is most typically examined using the calculation for fractional anisotropy (FA); described in Basser and Pierpaoli, 1996; applied in several manuscripts, e.g. Pfefferbaum et al., 2000; Abe et al., 2002), yet similar metrics such as relative anisotropy (RA) have also been applied in the diffusion-imaging literature examining lifespan changes (e.g. Huppi et al., 1998, 2001; Nusbaum et al., 2001; Miller et al., 2002; van Pul et al., 2005; Y. Zhang et al., 2005; Camara et al., 2007; Schneiderman et al., 2007; Stahl et al., 2007).

In some of the papers I have read on this fundamental process, ATP was also observed to lower the time-averaged phosphorescence anisotropy inside of cells, possibly via an interaction with the low-affinity regulatory site of the protein.

None of these things are controlled for in nnEMF toxicity studies.  When my @Bitcoinandbeef interview

CITES
https://www.sciencedirect.com/science/article/pii/B9780123964601000123

Cersosimo M. G., Koller W. C. (2006). The diagnosis of manganese-induced parkinsonism. Neurotoxicology 27, 340–346.

Lucchini R. G., Martin C. J., Doney B. C. (2009). From manganism to manganese-induced parkinsonism: A conceptual model based on the evolution of exposure. Neuromol. Med. 11, 311–321.

Hashimoto R., Mori T., Nemoto K., Moriguchi Y., Noguchi H., Nakabayashi T., Hori H., Harada S., Kunugi H., Saitoh O. (2009). Abnormal microstructures of the basal ganglia in schizophrenia revealed by diffusion tensor imaging. World J. Biol. Psychiatry 10, 65–69.

S. C. Glotzer and M. J. Solomon, Nature Mater. 6, 557 (2007).

S.-M. Yang, S.-H. Kim, J.-M. Lima, and G.-R. Yi, J. Mater. Chem. 18, 2177 (2008).

L. Rossi, S. Sacanna, and K. P. Velikov, Soft Matter 7, 64 (2011).

The newest innovation from El Salvador: ANABOLIC COMPUTING

video
play-sharp-fill

Watch the video above and head to daylightcomputer.com and use password KRUSE2023 to see more on this great innovation from Anjan Katta of Daylight Computer, based for now in San Francisco.  Below is my receipt as the first customer of this innovation.

BLUE LIGHT IS A STIMULANT THAT CREATES ROS/RNS NORMALLY

And stimulants are 👍 great. Most Americans drink a few cups of stimulants each morning ☕️ to get themselves up to face the daily grind.

But you know what’s not great? Being stimulated 24 hours of every day by blue light. This ruins the dose-response curve of the ROS/RNS. That is precisely what is occurring to modern humans because they live indoors and use tech screens excessively. What else is different about this version of blue light? The blue light that wakes us up in the sun is NEVER present without 42% IR-A light, which is red light.  AM sunlight has 42% red light in it and only 1600K of blue light. This small stimulus of blue light is about to improve the executive function of the prefrontal cortex. This blue light needs red light to control the oxidation ROS/RNS that blue light makes when it is present without red light in our light environment.

ALL CELLS contain ion channels in their outer (plasma) and inner (organelle) membranes. Like other proteins, Ion channels are targets of oxidative impact, which modulates ion fluxes across membranes. Subsequently, these ion currents affect electrical excitability, such as action potential discharge (in neurons, muscle, and receptor cells), alteration of the membrane resting potential, synaptic transmission, hormone secretion, muscle contraction, or coordination of the cell cycle.

An important class of ion channels is the family of potassium (K+) channels; they are not only in charge of the membrane resting potential or the repolarization of the action potentials but also control cell proliferation or transmitter/hormone release, to name a few. A subgroup of K+ channels are the so-called calcium (Ca2+) activated K+ channels, which need either an increase of Ca2+ at their intracellular face to open or a combination of Ca2+ and voltage to function correctly. Maxi Ca2+-activated K+ channels, also named BK channels, constitute a subgroup of Ca2+-activated K+ channels.

Do you know where these ion channels exist in humans?  They are found on the inner mitochondrial membrane. EXCESSIVE BLUE LIGHT exposure destroys these potassium ion channels to ruin signaling of cells that control the circadian mechanism and are associated with leptin and melanopsin. LET THAT SINK IN.

Mitochondria are a significant source of ROS generation targeting BK channels. Blue light creates that stimulus when RED LIGHT IS ABSENT.

C TERMINAL CHANGES ARE A BLUE LIGHT STORY.  

The inner membrane of mitochondria contains BK channels (mtBK), which appear essential in the production of ROS. mtBK channels appear to be inserted into the mitochondrial membrane with the toxin binding sites for charybdotoxin and iberiotoxin exposed to the mitochondrial intermembrane space. This can be accessed using outside-out patch configuration of the inner mitochondrial membrane. Consequently, the C-terminal tail domain, including the Ca2+ binding site, is localized to the mitochondrial matrix where the proton gradient exists.

RED LIGHT MOVES PROTONS BEST. Blue light creates the most ROS. Do you understand why subtracting red light and UV light from blue creates mitochondrial diseases now?

Your brain wakes up when you look at your computer or phone screen. It’s alert. Because it hears, “It’s daytime! Time to be focused and do human things!”

But guess when it’s terrible to hear that signal?

The other 14 hours of the day, the Sun wouldn’t usually send such a signal to the brain.

We need a break from the stimulus. Otherwise, we fry our circuits and get fatigued.

So take a break from the blue light our modern world worships. Stop the intravenous coffee to your SCN and allow yourself to relax.

WHY DO ALL HUMAN NEED THIS COMPUTER?  

This computer builds your brain anabolically and does not destroy it catabolically as every other computer does.  

WHY DOES ALAN (artificial light at night) or blue light cause melanoma?

Pyrimidine dimers are molecular lesions formed from thymine or cytosine bases in DNA via photochemical reactions. Ultraviolet light (UV) induces the formation of covalent linkages between consecutive bases along the nucleotide chain in the vicinity of their carbon–carbon double bonds. The dimerization reaction can also occur among pyrimidine bases in dsRNA (double-stranded RNA)—uracil or cytosine. Two everyday UV products are cyclobutane pyrimidine dimers (CPDs) and 6–4 photoproducts. Blue light causes these cyclobutane residues, which can lead to cancers like melanoma. Many people think UV light causes this, but blue light is way more potent in generating these melanoma-inducing chemicals, as shown below.

These pre-mutagenic lesions alter the structure and possibly the base-pairing in DNA. Up to 50–100 such reactions per second might occur in a skin cell during exposure to sunlight but are usually corrected within seconds by photolyase reactivation or nucleotide excision repair. Uncorrected lesions can inhibit polymerases, cause misreading during transcription or replication, or lead to arrest of replication.

You might not know pyrimidine dimers are humans’ primary cause of melanomas. Your dermatologist certainly does not know this science. https://www.nature.com/articles/s41467-020-16283-9

THIS IS NOT A MOUSE STUDY

Artificial man-made Blue Light “Enhances” Melatonin Suppression….via melanopsin damage………Imagine that?

🐭😱

I’m sorry, but we are still relatively close to the starting line when it comes to the amount of research into blue light and circadian rhythm so we kind of have to read what we have access to and do our best to be DIRECTIONALLY accurate in what we take from them and how they apply to humans.

This paper, however, is one of the best you’ll find anywhere.

They tested 24 humans. Some of whom, I’m told, actually look like mice.

They determined…

“Each fluence-response curve demonstrated that increasing corneal irradiances of light-evoked progressively increased nocturnal melatonin suppression. A comparison of these fluence-response curves supports the hypothesis that polychromatic fluorescent light is more potent for melatonin regulation when enriched in the short wavelength spectrum.”

Download this 30-page PDF beauty as an early Christmas present here:  https://jdc.jefferson.edu/cgi/viewcontent.cgi

WHY DO I WANT TO EXTINCT BLUE-BLOCKING GLASSES? 

Is there visual acuity flux in the human eyes due to variable factors in our light environment? Yes, there is. Black Swan MDs would be wise to recommend routine sunning the eyes to release stress in eye ciliary muscles to improve vision accommodation via dopamine modulation of the skeletal muscle fiber types in these eye muscles. Just knowing this data is true, one can’t help but wonder if prescription eyeglass wearers shouldn’t be evaluated in an eye doctor’s office over a series of days/times (diurnal exams) to account for these confounding lighting factors in determining overall average visual acuity. I’ve begun doing this for blue blockers. The results are quite interesting.  It caused me to ask Anjan to build this computer.  Blue locking glasses are not enough protection.  

Based on my work with patients, a computer with zero blue light emission is the requirement.  We will still need them for other things, but you won’t need them with Anjan’s computer.

There is a “revolution on the surface of the earth” called blue-lit technology, and it is causing a new evolution of free radical signals via nnEMF and magnetic fields from your environment, changing the internal terroir in your mitochondria, leading to diseases that appear to emerge from nowhere. Anjan’s computer puts a dent in this game plan hatched by Silicon Valley.  This is why they want him to fail.  The healthcare reality you obtain manifests from these collisions and creations.

SUMMARY

This conversation happened recently based on my work around decentralized medicine and anabolic computing in El Salvador.

Follow me closely with this, because this might be the most important post you read on Patreon in your entire life:

“I have known for years now that melatonin is anti-cancer. But every study I’ve read basically pegged it as such because of its antioxidant activities. This is true to an extent.

However, last night, a pretty brilliant neurosurgeon that I’ve been following for about five years now turned the light on in my mind and made it crystal clear to me precisely what the mechanism is that makes melatonin so crucial for cancer prevention and healing from cancer.

He made two statements:

1) blue (artificial) light, especially at night, causes cancer.

2) nnEMF (non-native electromagnetic fields – think cell phones, x-box, tablets, Wi-Fi routers, cell towers, smart meters, smart homes, Apple watches, Fitbit, Bluetooth, or anything that operates on wireless technology) causes cancer.

But here is the connection that he helped me make last night:

What is the hallmark trait of cancer? – dysfunctional cells that are like STEM CELLS that are multiplying and growing out of control in the body.

Here’s the rub: we ALL have cancer cells growing in our bodies. All of us. What makes it that one person doesn’t develop deadly cancers while others do?

One word: apoptosis. This describes the body’s innate ability to recognize a cell as dysfunctional and potentially cancerous and “orders” the cell to shut down and die.

The amount of melatonin controls apoptosis a mitochondrion can make, and our mitochondria make the most melatonin in our body. That amount is quantized to the light we live under.

If apoptosis works correctly in you, you will not develop cancer because your body can recognize those dysfunctional cells and neutralize them immediately. Problem solved.

Here’s the thing: MELATONIN, the hormone made in every mitochondria and found in our pineal gland created in the absence of LIGHT, regulates apoptosis. Let me make this plain as day for you (even if it is a crude description of a very complex biological process):

No melatonin = no apoptosis.

No apoptosis = dysfunctional cells growing out of control = CANCER.

Artificial light at night and nnEMF BOTH individually signal to your colony of mitochondria that it is daytime. In response, your colony of mitochondria and your pineal gland will dramatically reduce melatonin synthesis and output.

The light bulb was invented in the last 100 years, and homes across America have permanently changed how they live. What do we do when the sun goes down? We flip on the light switch and turn the computer. We sit on our phones. On our TVs and tablets.  We are using iPads as digital babysitters!

All of this lowers our melatonin and arrests the process of apoptosis.

We are literally handcuffing our body’s natural and brilliant defense mechanism against cancer!

THINK ABOUT THIS FOR A MOMENT!

In our lifetimes, research shows that 1 in 2 of us will develop cancer. This is a VERY sharp rise from even 50 years ago.

We give money to cancer research charities, who then give that money to cash-rich pharma companies who don’t need our money so they can create drugs that don’t cure cancer and make us go broke using them. We run, walk, and bike for the cure.

What if the cure for cancer was right under our noses?

What if it’s as simple as shutting off the damn lights when the sun goes down? Use a computer that has zero blue light.  We can all agree on using low amber lighting, wearing blue-blocking glasses, shutting off your Wi-Fi router, turning off your wireless devices, and instead of watching TV, hanging out and talking with your family and then going to bed early.

If it’s that simple to prevent cancer for you and your children, would you do it?

Below is a study that shows how melatonin regulates the apoptosis of cancer cells.

There are hundreds, if not thousands, of studies and research papers that show how artificial light at night suppresses melatonin and several studies that show how nnEMF does this as well.”

“Jack and Anjan might have solved one of the biggest riddles in the world. ”

CITES

1.  https://pubmed.ncbi.nlm.nih.gov/24920214/

2. THE SIZE OF THIS MARKET IS HUGE  https://bmcpsychology.biomedcentral.com/articles/10.1186/s40359-023-01166-7

3. https://www.socialworktoday.com/news/dn_121317.shtml

QUANTUM ENGINEERING #62: CENTRALIZED IDEAS ABOUT CANCER ARE 180 DEGREES FROM NATURE’S TRUTH

Tumor immunity represents a new avenue for cancer therapy. Immune checkpoint inhibitors have successfully improved outcomes in several tumor types. In addition, currently, immune cell-based therapy is also attracting significant attention. However, the clinical efficacy of these treatments requires further improvement. The mechanisms through which cancer cells escape the immune response must be identified and clarified. Cancer stem cells (CSCs) play a central role in multiple aspects of malignant tumors. CSCs can initiate tumors in partially immunocompromised mice, whereas non-CSCs fail to form tumors, suggesting that tumor initiation is a definitive function of CSCs. However, the fact that non-CSCs also initiate tumors in more highly immunocompromised mice suggests that the immune evasion property may be a more fundamental feature of CSCs rather than a tumor-initiating property.

What if stem cells’ “evasion-by-replication” strategy were the root of cancer when they are hit by vaccine particles?

What If human cancer theory is upside-down?

In my Rubin Huberman podcast I told that it is upside based on the light story.  It turns out it is upside down because of the SV-40 story uncovered by Sarah Stewart in the Cutter Incident too.  How?

Cancer cells are actively looking for a source of UV light to control the cell cycle.  Cells migrate when Ulraweak UV biophotons are absent from mitochondrial metabolism.

You’ll begin to see a new mitochondrial perspective of my advice.  Transfecting immuno privileged stem cells with SV-40 is a bad idea with horrible consequences.

COVID-vaccine-induced cancer data from the Ethical Skeptic demonstrate cancer genesis isn’t necessarily a long inexplicable number of somatic mutations like Philip Buckholdts wants you to believe.  Cancer genesis is contamination-induced and electromagnetic radiation increases contamination by DNA destruction which act as plasmids. The Covid aftermarket data now suggests 1 in 225 shots could trigger cancers.

People forget each octave of the electromagnetic spectrum has a particular energy associated with it and that energy links to how DNA is damaged.  For example, DNA replication errors, especially those occurring at regions that are hard to replicate, are called fragile sites.  These sites can cause breaks in DNA that results in pieces and parts of nDNA. This process alone can lead to cancer, primarily by making it more likely that fragments of chromosomes rearrange themselves, activating genes that lead to uncontrollable cell division.  Mary Sherman and Sarah Stewart invented this science in their bio-weapons lab in New Orleans.

What is the target that these two women trip over with their use of the LINAC?

Cancers can be categorized into two groups: those whose frequency increases with age, and those resulting from errors during mammalian development. The first group is linked to DNA replication through the accumulation of genetic mutations that occur during proliferation of developmentally acquired stem cells that give rise to and maintain tissues and organs.

These mutations, which result from DNA replication errors as well as environmental insults, fall into two categories; cancer driver mutations that initiate carcinogenesis and genome destabilizing mutations that promote aneuploidy through excess genome duplication and chromatid missegregation. Increased genome instability results in accelerated clonal evolution leading to the appearance of more aggressive clones with increased drug resistance.

The second group of cancers, termed germ cell neoplasia, results from the mislocation of pluripotent stem cells during early development. During normal development, pluripotent stem cells that originate in early embryos give rise to all of the cell lineages in the embryo and adult, but when they mislocate to ectopic sites, they produce tumors. Light is capable of causing this mislocation.  This is a transgenerational effect of the electromagnetic spectrum.  The LINAC use showed this and that is why the SV-40 virus was made uber virulent by Sherman and Stewart work in New Orleans for the CIA.

Geminin is the target of the light spectrum in mammals to protect it from cancer.

Remarkably, pluripotent stem cells, like many cancer cells, depend on the Geminin protein to prevent excess DNA replication from triggering DNA damage-dependent apoptosis. Apoptosis is controlled by ultraweak UV light generation by mitochondrial metabolism.  This link between the control of DNA replication during early development and germ cell neoplasia reveals Geminin as the target of light.  Big pharma and oncology want to use geminin as a potential chemotherapeutic target in the eradication of cancer progenitor cells.  Light is better than drugs because it has no side effects. All drugs carry the side effect risks.  Oncology favors drugs because they are patentable for the profiteers they serve in centralized healthcare.

In centralized medicine & science there should be strict observation and questioning.  This is key to finding a solution to a problem.  They do not want to find a solution because it destroys the business model of oncology.

  1. Observation: COVID vaccinations have already triggered many cancer, and a significant number of people have already died from cancer.
    Question: If supposedly viruses such as HPV trigger decades-long domino effect that leads to cancer, why do these vaccines accelerate it so much? Have we got it all wrong?
  2. Observation: The mechanism of action of COVID vaccines is to penetrate a cell, hack it, have it produce a protein to trigger antibodies, but also to trigger a T-cell attack on the contaminated cell.
    Question: How come normal cells have survived that vaccine contamination and morphed so quickly into a cancerous cell?
  3. Observation: When you dive into vaccine-induced case reports, you realize most vaccines are capable of triggering cancer.
    Question: How and why do different vaccine technologies, targeting different viruses or bacteria, all end up having the same effect? Isn’t there another more automatic process at play?

Cancerous cells have very distinct features that cannot be regained by normal cells over night. And the idea that any push genetic in any direction, would always end up with the same outcome is genetically or mathematically impossible.

So, what’s going on?

Centralized science in cancer believes the following:  The majority of cancers result from random mutations arising during DNA replication in the normal stem cells required during development and tissue maintenance. Differences in cancer risk among different tissues can be explained by the total number of stem cell divisions in those tissues.  Is this true based on the Covid data?  It is not.

That means something else is behind the numbers.  What is it?

SV-40 and the light you live in.

SUMMARY

Mammalian cancer cannot start in normal cells penetrated by vaccine particles, because  these cells will be destroyed by the immune system MHC complex.  The human immune system is highly efficient at clearing cancer cells via this mechanism. In humans, cancer can only be started in stem cell which are normally immune protected. So human cancer cells always have all the traits of a stem cell. That is not what centralized oncology believes.  What a coincidence? Cancer theory was always upside down.  And none of them knew that ultraweak UV bio-photons stimulate mitosis to get a stem cell out of normal immune protection. That implies UV light is the best chemotherapy one can have.  It also means it is the best therapy to use in vaccine induced cancer and injury like long COVID.

CPC #72: CAN YOU CREATE PROPAGANDA TO SELL ART?

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I dislike Thanksgiving but I have a tradition where I retell my family the story of how the CIA used the artworld to change public opinion and this program was used to help assinate a president when it became clear that human perception could be harnessed by propaganda.  Part of this story was retold to you in the podcast above.  Here is the second part of the story for you to digest once you finish your Thanksgiving dinner today.  I am warning you it may give some of you indigestion.

When I teach people about Bitcoin, I have two go-to stories about asymmetric values to explain how something worth so little can grow to something beyond your imagination.  One is the Louisiana Purchase, and the other is Gertrude Stein’s experience with Picasso.

By 1905, Picasso became a favorite of American art collectors Leo and Gertrude Stein. Leo told his sister that his work would become iconic and valuable.  She famously told Picasso I wouldn’t say I like your work, but I trust my brother’s eye for value.  She began to collect Picasso’s early works for 5-20 dollars a painting.  Today, some of those paintings are worth 400 million dollars in private peer-to-peer deals.  These deals mimic the peer-to-peer network in Bitcoin.  The value of Bitcoin has gone from 1 cent to 69,000 in 13 years.

Alice B. Toklas (pictured above on right) is remembered for being Gertrude Stein’s (left) great love and writing her unusual, revered memoir-disguised-as-cookbook chronicling their life together. On September 8, 1907, her first day as an American expat in Paris, Toklas met Stein. The two fell instantly in love and remained together for the next 39 years until Stein’s death in 1946.

After Gertrude died, her collection of 47 paintings (38 of which were by Picasso) was bequeathed to her nephew but remained on the walls of Toklas’s home. Gertrude’s nephew eventually passed ownership on to his three children, who decided to sell when Toklas died in 1967.  Nelson Rockerfeller mother founded the Museum of Modern Art in NYC, and Nelson Rockerfeller was given the chance to buy from Stein’s collection first by the political powers that were in place at this time.

The number of MoMA-CIA crossovers is highly suspicious, to say the least when one reviews the history.

In the years since his death in 1973, Picasso’s stature as an artist elevated to the highest ranks, with some of his works going for more than $100 million in public auctions and reportedly at even higher sums in private deals. He remains the top-grossing artist at auction worldwide, raking $245 million across 3,400 lots in 2020 alone.  He is, in many ways, today’s “Bitcoin Standard” of the art market.

For example, Picasso’s Delacroix-inspired Les femmes d’Alger ‘Version O’ (1955) for $179.4 million in 2015 to Steve Wynn.

Femme Assise, pictured above, sold for 63 million dollars.  It depicts French artist and model Fernande Olivier, who went with Picasso to a remote village in Spain during the summer of 1909. While there, she posed for a number of his pictures.

PROPAGANDA AROUND ART WAS BORN IN TULANE UNIVERSITY’S MK-ULTRA

The Cold War was the most powerful macropolitical thing on the planet in the late 1940s and 1950s.

The CIA fostered and promoted American Abstract Expressionist painting worldwide for over 20 years.  The USSR of Stalin post WW2 was about total centralization in all things.  The CIA began experimenting with decentralization at this time in reaction to absolute centralization in the USSR.

The artists the CIA supported emphasize free, spontaneous, and personal emotional expression, and they exercise considerable freedom of technique and execution to attain this goal, with a particular emphasis laid on the exploitation of the variable physical character of paint to evoke expressive qualities (e.g., sensuousness, dynamism.)  The CIA task was monumental because few Americans liked decentralized art in the 1950s.  MK-ULTRA propaganda techniques were applied to change this perception.  It was so successful that it also bleed into the CIA’s operations involved in the assassinations of JFK and RFK Sr.

This was a period when the great majority of Americans disliked or even despised modern art – President Truman summed up the popular view when he said: “If that’s art, then I’m a Hottentot.” As for the artists themselves, many were ex-communists barely acceptable in the America of the McCarthyite era of the 50s, and certainly not the sort of people usually likely to receive US government backing.

Who were the artists the CIA supported?

Clyfford Still, Theodoros Stamos, Jackson Pollock, Willem de Kooning, Arshile Gorky, Mark Rothko, Lee Krasner, Robert Motherwell, Franz Kline, Adolph Gottlieb, David Smith, Hans Hofmann, Joan Mitchell are a few.

The connection between the CIA and art is improbable until you know what MK-ULTRA was all about.  Many of you heard about this program for the first time in my RFK Jr interview linked above.

This new artistic movement was propped up to be proof of the creativity, intellectual freedom, and cultural power of the US. Russian art, strapped into the communist ideological straitjacket, could not compete.

GENERAL GROVES GOT THIS IDEA FROM BERNAYS AND NAZI PROPAGANDA USED IN WW2

Many have forgotten General Groves was the most powerful man in the USA in WW2.  He controlled the Manhattan Project from start to finish.  He was the architect of the Cold War.  He single handedly reversed the promise that FDR made to Stalin at Potsdam that the USA would rebuild Russia for the sacrifices Russia made in defeating the Nazi’s in Europe.  The picture below is when FDR made this promise to Stalin right before FDR death.

Groves made sure that the DNC had replaced FDR’s Vice President before his fourth term so that Groves could control the power struggle that would result after Germany was defeated.  Groves knew that FDR was sympathetic to Stalin.  Groves wanted to limit emotion in post war politics because he realized that a chronic war was a powerful way to subvert the power in the executive branch.  War allowed for emergency power to be instituted without much controversy.  This allowed the industrial military complex to operate freely and covertly.  General groves wanted this ability to continue after the war.  Groves made sure the OSS office would become a central intelligence post in post war America by installing his own people.  Dulles was his hand picked successor.  Truman was Groves hand picked president because he could be easily manipulated by propaganda Groves created and the CIA propagated.

HOW DID THIS PROPAGANDA MACHiNE WORK IN THE ART WORLD?

The existence of this supportive policy in the art world in post war America, which had been rumored and disputed for many years, has now been confirmed for the first time by former CIA officials. Unknown to the artists, the new American art was secretly promoted under a policy known as the “long leash” – arrangements similar in some ways to the indirect CIA backing of the journal ENCOUNTER, edited by Stephen Spender.

The decision to include culture and art in the US Cold War arsenal was taken as soon as the CIA was founded in 1947 by Truman at General Groves’s request.  This was how the industrial, military complex captured the executive branch of government in the USA.  I covered this in the tweet thread cited below.

Dismayed at the appeal communism still had for many intellectuals and artists in the West, the new agency set up a division, the Propaganda Assets Inventory, which could influence more than 800 newspapers, magazines, and public information organizations at its peak. They joked that it was like a Wurlitzer jukebox: when the CIA pushed a button, it could hear whatever tune it wanted playing across the world.

The following key step came in 1950 when the International Organizations Division (IOD) was set up under Tom Braden. It was this office that subsidized the animated version of George Orwell’s Animal Farm, which sponsored American jazz artists, opera recitals, and the Boston Symphony Orchestra’s international touring program. Its agents were placed in the film industry, in publishing houses, and even as travel writers for the celebrated Fodor guides. And, we now know, it promoted America’s anarchic avant-garde movement, Abstract Expressionism in the art world.

Initially, more open attempts were made to support the new American art. In 1947 the State Department organized and paid for a touring international exhibition entitled “Advancing American Art,” with the aim of rebutting Soviet suggestions that America was a cultural desert. But the show caused outrage at home, prompting Truman to make his Hottentot remark and one bitter congressman to declare: “I am just a dumb American who pays taxes for this kind of trash.” The tour had to be canceled.

The US government now faced a dilemma. This philistinism, combined with Joseph McCarthy’s hysterical denunciations of all that was avant-garde or unorthodox, was deeply embarrassing. Many of you might have forgotten that RFK Sr worked under Joe McCarthy during these anti-communist times and this theme would come back to haunt the Kennedy family in November of 1963 and in 1968.

It discredited the idea that America was a sophisticated, culturally rich democracy. It also prevented the US government from consolidating the shift in cultural supremacy from Paris to New York since the 1930s. To resolve this dilemma, the CIA was brought in to change perception by using mind control techniques developed in the MK-Ultra program.

ALLEN DULLES WAS A GENERAL GROVES ACOLYTE AND HE WAS THE ARCHITECT OF THE KENNEDY DEATHS in 1963 and 1968.

ON APRIL 10, 1953, ALLEN DULLES became the newly APPOINTED DIRECTOR OF THE CIA, and he delivered a speech to a gathering of Princeton alumni. Though the event was mundane, global tensions were running high. The Korean War was coming to an end, and earlier that week, The New York Times had published a startling story asserting that American POWs returning from the country may have been “converted” by “Communist brain-washers.”  This was classic Cold War propaganda born in the work of Edward Bernays. Dulles decided to use this technique on the people of the United States.

Some GIs were confessing to war crimes, like carrying out germ warfare against the Communists–a charge the U.S. categorically denied. Others were reportedly so brainwashed that they refused to return to the United States at all. As if that weren’t enough, the U.S. was weeks away from secretly sponsoring the overthrow of a democratically elected leader in Iran to install the Shah to gain control of the oil fields in the Middle East.  The blow back of this CIA program would haunt future presidents.

DULLES EMPLOYED BERNAYS and GOEBBELS PROPAGANDA MACHINE ON THE US PUBLIC

Dulles had just become the first civilian director of an agency growing more powerful by the day, and the speech provided an early glimpse into his priorities for the CIA. “In the past few years, we have become accustomed to hearing much about the battle for men’s minds–the war of ideologies,” he told the attendees. “I wonder, however, whether we clearly perceive the magnitude of the problem, whether we realize how sinister the battle for men’s minds has become in Soviet hands,” he continued. “We might call it, in its new form, ‘brain warfare.’”

Dulles proceeded to describe the “Soviet brain perversion techniques” as effective but “abhorrent” and “nefarious.” He gestured to the American POWs returning from Korea, shells of the men they once were, parroting the Communist propaganda they had heard cycled for weeks on end. He expressed fears and uncertainty–were they using chemical agents? Hypnosis? Something else entirely? “We in the West,” the CIA Director conceded, “are somewhat handicapped in brain warfare.” This sort of non-consensual experiment, even on one’s enemies, was antithetical to American values, Dulles insisted, as well as antithetical to what should be human values.  Behind the scenes Dulles was building a CIA program to mimic what the communists and Nazi’s had already done.

Newspaper headlines like “New Evils Seen in Brainwashing” and “Brainwashing vs. Western Psychiatry” offered sensational accounts of new mind-control techniques and technologies that no man could fully resist. The paranoia began to drift into American culture, with books like The Manchurian Candidate and The Naked Lunch playing on themes of unhinged scientists and vast political conspiracies.  These current events in the newspapers were like a shark fin breaking the water, announcing to the public that the CIA had an active mind control program at the covert universities in the Deep South.  This is why MK-Ultra was born and bred at Tulane University.  I mentioned this in the RFK Jr Tetragrammaton podcast .

MK-ULTRA AT TULANE linked to museums, the media, and CBS

Three days after his speech decrying Soviet tactics, Dulles approved the beginning of MK-Ultra, a top-secret CIA program for “covert use of biological and chemical materials.” “American values” made for good rhetoric, but Dulles had far grander plans for the agency’s Cold War agenda.

MK-Ultra’s “mind control” experiments generally centered around behavior modification via electro-shock therapy, hypnosis, polygraphs, many forms radiation, artificial light and a variety of drugs, toxins, and chemicals. These experiments relied on a range of test subjects: some who freely volunteered, some who volunteered under coercion, and some who had absolutely no idea they were involved in a sweeping defense research program. From mentally-impaired boys at a state school to American soldiers to “sexual psychopaths” at a state hospital, MK-Ultra’s programs often preyed on the most vulnerable members of society.

The CIA targeted cities in the USA for testing as well.  St Louis and SF were two of the best documented in this program.  The CIA considered prisoners especially good subjects, as they were willing to give consent in exchange for extra recreation time or commuted sentences.  Recall how they tested the SV-40 concentrated virus by the LINAC on an Angola death row inmate in August of 1963 to test their bioweapons to kill Castro.  MK-Ultra gave birth to this program in the bioweapons lab run by Dr. Alton Ochsner (middle below) and Dr. Mary Sherman (second pic below).

Whitey Bulger, a former organized crime boss, wrote of his experience as an inmate test subject in MK-Ultra. “Eight convicts in a panic and paranoid state,” Bulger said of the 1957 tests at the Atlanta penitentiary where he was serving time. “Total loss of appetite. Hallucinating. The room would change shape. Hours of paranoia and feeling violent. We experienced horrible periods of living nightmares and even blood coming out of the walls. Guys turning to skeletons in front of me. I saw a camera change into the head of a dog. I felt like I was going insane.”

Bulger claimed he had been injected with LSD. Lysergic acid diethylamide, or acid, had become one of the CIA’s critical interests for its “brain warfare” program, as the agency theorized it could be useful in interrogations. In the late 1940s, the CIA received reports that the Soviet Union had engaged in “intensive efforts to produce LSD,” and that the Soviets had attempted to purchase the world’s supply of the chemical. One CIA officer described the agency as “literally terrified” of the Soviets’ LSD program, largely because of the lack of knowledge about the drug in the United States. “[This] was the one material that we had ever been able to locate that really had potential fantastic possibilities if used wrongly,” the officer testified.

All this went on right before the bioweapons program that began in the USA in New Orleans in 1950-1964.  You need to understand the timeline of history to understand what is going on today in your world.  Experiments with LSD was the precursor to the SV-40 experiments.

With the advent of MK-Ultra, the government’s interest in LSD shifted from a defensive to an offensive orientation. Agency officials noted that LSD could be potentially useful in “[gaining] control of bodies whether they were willing or not.” The CIA envisioned applications that ranged from removing people from Europe in the case of a Soviet attack to enabling assassinations of enemy leaders. On November 18, 1953, a group of ten scientists met at a cabin deep in Maryland’s forests. After extended discussions, the participants agreed that to understand the value of the drug truly, “an unwitting experiment would be desirable.”

ART AND MK-ULTRA MERGE

The connection between art and propaganda is not quite as odd as it might appear once you see it from this perspective. At this time, the new agency, staffed mainly by Yale and Harvard graduates, many of whom collected art and wrote novels in their spare time, was a haven of liberalism when compared with a political world dominated by McCarthy or with J Edgar Hoover’s FBI. If any official institution was in a position to celebrate the collection of Leninists, Trotskyites, and heavy drinkers that made up the New York School, it was the CIA.

Until now, there has been no first-hand evidence to prove that this connection was made, but for the first time, a former case officer, Donald Jameson, has broken the silence. Yes, he has said, the agency saw Abstract Expressionism as an opportunity, and it ran with it.

“Regarding Abstract Expressionism, I’d love to be able to say that the CIA invented it just to see what happens in New York and downtown SoHo tomorrow!” he joked. “But I think that what we did really was to recognize the difference. It was recognized that Abstract Expressionism was the kind of art that made Socialist Realism look even more stylized and more rigid and confined than it was. And that relationship was exploited in some of the art exhibitions.

“In a way, our understanding was helped because Moscow in those days was very vicious in denouncing any kind of non-conformity to its own very rigid patterns. And so one could quite adequately and accurately reason that anything they criticized that much and that heavy-handedly was worth support one way or another.”

To pursue its underground interest in America’s lefty avant-garde, the CIA had to be sure its patronage could not be discovered. “Matters of this sort could only have been done at two or three removes,” Mr. Jameson explained, “so there wouldn’t be any question of having to clear Jackson Pollock, for example, or do anything that would involve these people in the organization. And it couldn’t have been any closer because most of them were people who had very little respect for the government, in particular, and certainly none for the CIA. If you had to use people who considered themselves one way or another to be closer to Moscow than to Washington, well, so much the better, perhaps.”

This was the “long leash”. The centerpiece of the CIA campaign became the Congress for Cultural Freedom, a vast jamboree of intellectuals, writers, historians, poets, and artists which was set up with CIA funds in the early 1950s and run by a CIA agent. It was the beachhead from which culture could be defended against the attacks of Moscow and its “fellow travelers” in the West. At its height, it had offices in 35 countries and published over two dozen magazines, including Encounter.

SV-40 SIDEBAR OCCURING AT THE SAME TIME THE CIA WAS USING THE ART WORLD

The success of this program preconditioned the CIA to believe they could build a covert bioweapons lab in the USA and hide it below the noses of the public and keep it covert using propaganda.  These same facades where used to link neo-con community of Ochsner to the gay  underground community Clay Shaw and David Ferry were in New Orleans.  This was how the CIA came to link the medical and gay community in the conspiracy to kill JFK.   just look at the familiar links used in the art world via MK-Ultra and the ones I revealed in the RFK Jr podcast.

HOW DID THE CIA USE MODERN ART COVERTLY?  IT CORRUPTED THE MEDIA AT THE SAME TIME

The Congress for Cultural Freedom also gave the CIA the ideal front to promote its covert interest in Abstract Expressionism. It would be the official sponsor of touring exhibitions; its magazines would provide useful platforms for critics favorable to the new American painting, and no one, the artists included, would be any the wiser.

This organization put together several exhibitions of Abstract Expressionism during the 1950s. One of the most significant, “The New American Painting,” visited every big European city in 1958-59. Other influential shows included “Modern Art in the United States” (1955) and “Masterpieces of the Twentieth Century” (1952).

Because Abstract Expressionism was expensive to move around and exhibit, millionaires, and museums were called into play. Nelson Rockefeller, whose mother had co-founded the Museum of Modern Art in New York, was pre-eminent among these. As president of what he called “Mummy’s Museum,” Rockefeller was one of the biggest backers of Abstract Expressionism (which he called “free enterprise painting”). His museum was contracted to the Congress for Cultural Freedom to organize and curate most of its important art shows.

The museum was also linked to the CIA by several other bridges that most of the American public is ignorant of.   This is how the First Amendment of the United States was captured by the CIA.

William Paley, the president of CBS Broadcasting and a founding father of the CIA, sat on the members’ board of the museum’s International Program. John Hay Whitney, who had served in the agency’s wartime predecessor, the OSS, was its chairman. The Whitney museum of modern art sat on 75th and Madison Ave in New York City.  I lived as a child in this neighborhood and was well aware of its history at an early age.  Did you know that Tom Braden, first chief of the CIA’s International Organizations Division (IOD), was executive secretary of the museum in 1949?

Do you know who worked for William Paley in Dallas in 1963 and later became their network star?

Dan Rather used propaganda in his reporting to help his boss cover up the CIA operations that occurred 60 years ago yesterday.

Now dead, Mr Braden lived in Woodbridge, Virginia until 2009, in a house packed with Abstract Expressionist works and guarded by enormous Alsatians. He explained the purpose of the IOD.

Baden said, “we wanted to unite all the people who were writers, who were musicians, who were artists, to demonstrate that the West and the United States were devoted to freedom of expression and to intellectual achievement, without any rigid barriers as to what you must write, and what you must say, and what you must do, and what you must paint, which was what was going on in the Soviet Union. I think it was the most important division that the agency had, and I think that it played an enormous role in the Cold War.”

He confirmed that his division had acted secretly because of the public hostility to the avant-garde: “It was very difficult to get the 1950s anti-communist Congress to go along with some of the things we wanted to do – send art abroad, send symphonies abroad, publish magazines abroad. That’s one of the reasons it had to be done covertly. It had to be a secret.  In order to encourage openness, we believed it had to be secret.”

If this meant that the CIA had to play the role of the Pope to this century’s Michelangelos, well, all the better: “It takes a pope or somebody with a lot of money to recognize art and to support it,” Mr. Braden said. “And after many centuries, people say, ‘Oh look! the Sistine Chapel, the most beautiful creation on Earth!’ It’s a problem that civilization has faced ever since the first artist and the first millionaire or Pope who supported him. And yet, if it hadn’t been for the multi-millionaires or the popes, we wouldn’t have had the art.”

Would Abstract Expressionism have been the dominant art movement of the post-war years without this CIA patronage? The answer is questionable to those outside the art world.  Those inside of it would likely disagree.  I have been of the opinion for a long time now, that it would not be wrong to suggest that when you look at an Abstract Expressionist painting, you are being duped by the CIA propaganda.  Today, I am thankful to bring you this story I have told to my family at Thanksgiving because this year after the Tetragrammaton podcast with RFK Jr you can now fully understand how all the parts fit to explain US history the military wants you to forget.

But look where this art ended up: in the marble halls of banks, in airports, in city halls, boardrooms, and great galleries. For the Cold Warriors who promoted them, these paintings were a logo, a signature for their culture and system, which they wanted to display everywhere that counted. The CIA propaganda program succeeded in a big way.

The Covert Art Operation continues to bleed into the New Orleans bioweapons lab

In 1958, the touring exhibition “The New American Painting”, including works by Pollock, de Kooning, Motherwell, and others, was on show in Paris. The Tate Gallery was keen to have it next but could not afford to bring it over. Late in the day, an American millionaire and art lover, Julius Fleischmann, stepped in with the cash, bringing the show to London.

However, the money that Fleischmann provided was not his, but the CIA’s. It came through a body called the Farfield Foundation, of which Fleischmann was president, but far from being a millionaire’s charitable arm, the foundation was a secret conduit for CIA funds.  This was how Ochsner got his LINAC from a Hill Burton Grant that the politicians who controlled the industrial military complex controlled in the 1950s.  Amazing coincidence don’t you think?

So, unknown to the Tate, the public, or the artists, the exhibition was transferred to London at American taxpayers’ expense to serve subtle Cold War propaganda purposes. A former CIA man, Tom Braden, described how such conduits as the Farfield Foundation were set up. “We would go to somebody in New York who was a well-known rich person, and we would say, ‘We want to set up a foundation.’ We would tell him what we were trying to do and pledge him to secrecy, and he would say, ‘Of course, I’ll do it,’ and then you would publish a letterhead, and his name would be on it, and there would be a foundation. It was really a pretty simple device.”  This is what the CIA did with Dr. Alton Ochsner in the 1950s after the Cutter Incident.

Julius Fleischmann was well-placed for such a role. He sat on the International Program of the Museum of Modern Art in New York board, as did several powerful figures close to the CIA.  Many Americans in 2023 still do not know how art and the CIA were linked by propaganda.

The world today exists on a belief system that “those in power” can outrun the truth by using intelligence agencies and their technology by manipulating money in the art world – without consequences.   The reality of the situation is that the world of art TODAY still is ruled by the consequences that CIA propaganda used to rehypothecate money to manipulate public opinion.  They used the art world to create and steal money forever wars in the pre Vietnam era and today they are creating trillions of dollars in cancer patients to create massive piles of fiat money they can funnel from HHS to the DOD and CIA to run the chronic wars today.

MK-ULTRA DEMISE WAS AT THE HAND OF ANOTHER KENNEDY

In 1977, Senator Edward Kennedy oversaw congressional hearings investigating the effects of MK-Ultra. Congress brought in a roster of ex-CIA employees for questioning, interrogating them about who oversaw these programs, how participants were identified, and if any of these programs had been continued. The Hearings turned over a number of disturbing details, particularly about the 1953 suicide of Dr. Frank Olson, an Army scientist who jumped out of a hotel window several days after unwittingly consuming a drink spiked with LSD. Amid the growing criminalization of drug users, and just a few years after President Nixon declared drug abuse as “public enemy number one,” the ironies of the U.S.’s troubling experimentation with drugs appeared in sharp relief.

But throughout the hearings, Congress kept hitting roadblocks: CIA staffers claimed they “couldn’t remember” details about many of the human experimentation projects or even the number of people involved. The obvious next step would be to consult the records, but that presented a small problem: in 1973, amid mounting inquiries, the director of MK-Ultra told workers, “It would be a good idea if [the MK-Ultra] files were destroyed.” Citing vague concerns about the privacy and “embarrassment” of participants, the men who crafted MK-Ultra effectively eradicated the paper record for one of the United States’ most obviously illegal undertakings. A program born in secrecy would hold onto many of its secrets forever because the government covered its own illegal tracks.

SUMMARY

Remember what John D. Rockefeller promised Congress under the administration of Teddy Roosevelt that the Rockefeller family would bankrupt the US government one day for breaking up the Standard Oil Trust.  The relationship between Modern Art and American diplomacy began during WWII when the Museum of Modern Art was mobilized for the war effort. MoMA was founded in 1929 by Abby Aldrich Rockefeller. A decade later, her son, Nelson Rockefeller, became president of the Museum. In 1940, while he was still President of MoMA, Rockefeller was appointed the Roosevelt Administration’s Coordinator of Inter-American Affairs. He also served as Roosevelt’s Assistant Secretary of State in Latin America.

The Museum followed suit. MoMA fulfilled 38 government contracts for cultural materials during the Second World War and mounted 19 exhibitions of contemporary American painting for the Coordinator’s office, which were exhibited throughout Latin America. Latin America is where Dr. Alton Ochsner made most of his fortune while he was alive.  He offered medical sanctuary to all the dictators of Latin America.

This direct relationship between the avant-garde and the war effort was well suited: The term avant-garde began as a French military term describing vanguard troops advancing into battle.

In the battle for “hearts and minds,” modern art was particularly effective. John Hay Whitney, both a president of MoMA and a member of the Whitney Family, which founded the Whitney Museum of American Art, explained that art stood out as a line of national defense because it could “educate, inspire, and strengthen the hearts and wills of free men.”

Whitney succeeded Rockefeller as President of the Museum of Modern Art in January 1941 so Nelson could turn his entire attention to his Coordinator duties. Under Whitney, MoMA served as “A Weapon of National Defense.” According to a Museum press release dated February 28, 1941, MoMA would “inaugurate a new program to speed the interchange of the art and culture of this hemisphere among all the twenty-one American republics.”

The goal was “Pan-Americanism.” This was the environment that Dr. Alton Ochsner was operating in during the 1950s-60s during the Cutter Incident.  Ochsner Medical Foundation Hospital had every Latin American flag outside of it for close to 40 years.  I know because I saw them every day for 6 years of my residency in New Orleans.

A “Traveling Art Caravan” through Latin America “would do more to bring us together as friends than ten years of commercial and political work.”

When World War 2 ended, Nelson Rockefeller returned to the Museum, and his Inter-American-Affairs staffers assumed responsibilities for MoMA’s international exhibition program: René d’Harnoncourt, who had headed Inter-American’s art division, became the Museum’s vice president in charge of foreign activities. Fellow staffer Porter McCray became the Director of the Museum’s International Program.

Modern art was so well aligned with American Cold War foreign policy that McCray took a leave of absence from the Museum in 1951 to work on the Marshall Plan. In 1957, Whitney resigned his position as MoMA’s Chairman of the Board of Trustees to become United States Ambassador to Great Britain. Whitney remained a trustee of the Museum while he was Ambassador, and his successor as Chairman was… Nelson Rockefeller, who had served as Special Assistant to President Eisenhower for Foreign Affairs until 1955.  Who was his VP?  Nixon.  Who is seated right next to Dr. Ochsner below?  His policies began the The War on Cancer in 1971.  This is another propaganda technique born at the same time the USD dollar was removed from the gold standard. You are all unaware of the tangled webs the CIA has woven to confuse you to get their agenda through.

In 1947, at the very moment that the Advancing American Art show was being recalled, and the United States Government was selling its O’Keeffe’s for fifty bucks a piece (all seventy-nine pieces in the show together brought in $5,544), the CIA was being created. The CIA grew out of “Wild” Bill Donovan’s Office of Strategic Services (OSS), which was the U.S.’s wartime intelligence apparatus. The OSS became the CIA and George H. Bush Father ran that office.

George W. Bush’s grandfather, the late US senator Prescott S. Bush, was a director and shareholder of companies that profited from their involvement with the financial backers of Nazi Germany.

The Guardian newspaper in the UK obtained confirmation from newly discovered files in the US National Archives that a firm of which Prescott S. Bush was a director was involved with the financial architects of Nazism.  He worked directly with Joseph Goebbels the Nazi Propaganda chief.  Imagine that.

His business dealings, which continued until his company’s assets were seized in 1942 under the Trading with the Enemy Act, has led more than 60 years later to a civil action for damages being brought in Germany against the Bush family by two former slave laborers at Auschwitz.  This only caused a minor ripple in the US Press during his pre-election in 2000.  Guess why?  The media was already captured by his friends in the CIA decades before this controversy.

The evidence the Guardian found has also prompted one former US Nazi war crimes prosecutor to argue over 80 years ago that the late senator’s action should have been grounds for prosecution for giving aid and comfort to the enemy.

What is the evidence against the Bush family and their oil empire?

While there is no suggestion that Prescott Bush was sympathetic to the Nazi cause, the documents reveal that the firm he worked for, Brown Brothers Harriman (BBH), acted as a US base for the German industrialist, Fritz Thyssen, who helped finance Hitler in the 1930s before falling out with him at the end of the decade. We now have confirmed published evidence from US government archives that shows Bush was the director of the New York-based Union Banking Corporation (UBC) that represented Thyssen’s US interests and he continued to work for the bank after America entered WW2.

Bush was also on the board of at least one of the companies that formed part of a multinational network of front companies to allow Thyssen to move assets around the world.

Thyssen owned the largest steel and coal company in Germany and grew rich from Hitler’s efforts to re-arm between the two world wars. One of the pillars in Thyssen’s international corporate web, UBC, worked exclusively for, and was owned by, a Thyssen-controlled bank in the Netherlands. More tantalizing are Bush’s links to the Consolidated Silesian Steel Company (CSSC), based in mineral rich Silesia on the German-Polish border. During the war, the company made use of Nazi slave labor from the concentration camps, including Auschwitz.

The ownership of CSSC changed hands several times in the 1930s, but documents from the US National Archive declassified in 2003 that link Bush to CSSC, although it is not clear if he and UBC were still involved in the company when Thyssen’s American assets were seized in 1942.

Three sets of archives spell out Prescott Bush’s involvement. All three are readily available, thanks to the efficient US archive system and a helpful and dedicated staff at both the Library of Congress in Washington and the National Archives at the University of Maryland.  You should fact check Uncle Jack.

The third set of documents, are also at the National Archives, are contained in the files on IG Farben, who was prosecuted for war crimes in Neuremberg.

A report issued by the Office of Alien Property Custodian in 1942 stated of the companies that “since 1939, these (steel and mining) properties have been in possession of and have been operated by the German government and have undoubtedly been of considerable assistance to that country’s war effort”.

Prescott Bush, a 6ft 4in charmer with a rich singing voice, was the founder of the Bush political dynasty and was once considered a potential presidential candidate himself. Like his son, George, and grandson, George W, he went to Yale where he was, again like his descendants, a member of the secretive and influential Skull and Bones student society. He was an artillery captain in the first world war and married Dorothy Walker, the daughter of George Herbert Walker, in 1921.

In 1924, his father-in-law, a well-known St Louis investment banker, helped set him up in business in New York with Averill Harriman, the wealthy son of railroad magnate E H Harriman in New York, who had gone into banking.

One of the first jobs Walker gave Bush was to manage UBC. Bush was a founding member of the bank and the incorporation documents, which list him as one of seven directors, show he owned one share in UBC worth $125.  You may now understand why the Bush family favors a CBDC over Bitcoin now.  You may also understand why the Bush family is no friend to anyone named Kennedy.  They had a hand in JFK and RFK Sr. demises.

The bank was set up by Harriman and Bush’s father-in-law to provide a US bank for the Thyssens, Germany’s most powerful industrial family.

August Thyssen, the founder of the dynasty had been a major contributor to Germany’s first world war effort and in the 1920s, he and his sons Fritz and Heinrich established a network of overseas banks and companies so their assets and money could be whisked offshore if threatened again.

By the time Fritz Thyssen inherited the business empire in 1926, Germany’s economic recovery was faltering under Weimar hyperinflation. After hearing Adolf Hitler speak, Thyssen became mesmerized by the young firebrand. He joined the Nazi party in December 1931 and admits backing Hitler in his autobiography, I Paid Hitler, when the National Socialists were still a radical fringe party. He stepped in several times to bail out the struggling party: in 1928 Thyssen had bought the Barlow Palace on Briennerstrasse, in Munich, which Hitler converted into the Brown House, the headquarters of the Nazi party. The money came from another Thyssen overseas institution, the Bank voor Handel en Scheepvarrt in Rotterdam.

By the late 1930s, Brown Brothers Harriman, which claimed to be the world’s largest private investment bank, and UBC had bought and shipped millions of dollars of gold, fuel, steel, coal and US treasury bonds to Germany, both feeding and financing Hitler’s build-up to war.  Interesting history lesson huh?  I hope you do not choke on your turkey today.

Between 1931 and 1933 UBC bought more than $8m worth of gold, of which $3m was shipped abroad. According to documents now published in many books and FOIA requests, after UBC was set up it transferred $2m to BBH accounts and between 1924 and 1940 the assets of UBC hovered around $3m, dropping to $1m only on a few occasions.

In 1941, Thyssen fled Germany after falling out with Hitler but he was captured in France and detained there for the remainder of the war.

Mind you, there was nothing illegal in doing business with the Thyssens throughout the 1930s and many of America’s best-known business names invested heavily in the German economic recovery.  This seems ironic when you see how the Biden administration treats corporations who do business with Russia today over Ukraine.   The play book continues for the Deep State.

However, everything changed politically after Germany invaded Poland in 1939 because the covert plan could no longer stay hidden. Even then it could be argued that BBH was within its rights continuing business relations with the Thyssens until the end of 1941 as the US was still technically neutral until the attack on Pearl Harbor in 1941. The trouble started on July 30 1942 when the New York Herald-Tribune ran an article entitled “Hitler’s Angel Has $3m in US Bank”. UBC’s huge gold purchases had raised suspicions that the bank was in fact a “secret nest egg” hidden in New York City for Thyssen and other Nazi bigwigs. The Alien Property Commission (APC) launched an investigation.  It turns out the Bush family did hide Nazi assets during the war.  This is how the modern neo-cons were born in the US politics.

There is no dispute over the fact that the US government seized a string of assets controlled by BBH – including UBC and SAC – in the autumn of 1942 under the Trading with the Enemy Act. What is in dispute is if Harriman, Walker and Bush did more than own these companies on paper.

Erwin May, a treasury attache and officer for the department of investigation in the APC, was assigned to look into UBC’s business. The first fact to emerge was that Roland Harriman, Prescott Bush and the other directors didn’t actually own their shares in UBC but merely held them on behalf of Bank voor Handel. Strangely, no one seemed to know who owned the Rotterdam-based bank, including UBC’s president.

May wrote in his report of August 16 1941: “Union Banking Corporation, incorporated August 4 1924, is wholly owned by the Bank voor Handel en Scheepvaart N.V of Rotterdam, the Netherlands. My investigation has produced no evidence as to the ownership of the Dutch bank. Mr Cornelis [sic] Lievense, president of UBC, claims no knowledge as to the ownership of the Bank voor Handel but believes it possible that Baron Heinrich Thyssen, brother of Fritz Thyssen, may own a substantial interest.”

May cleared the bank of holding a golden nest egg for the Nazi leaders but went on to describe a network of companies spreading out from UBC across Europe, America and Canada, and how money from voor Handel travelled to these companies through UBC.

By September May had traced the origins of the non-American board members and found that Dutchman HJ Kouwenhoven – who met with Harriman in 1924 to set up UBC – had several other jobs: in addition to being the managing director of voor Handel he was also the director of the August Thyssen bank in Berlin and a director of Fritz Thyssen’s Union Steel Works, the holding company that controlled Thyssen’s steel and coal mine empire in Germany.

Within a few weeks, Homer Jones, the chief of the APC investigation and research division sent a memo to the executive committee of APC recommending the US government vest UBC and its assets. Jones named the directors of the bank in the memo, including Prescott Bush’s name, and wrote: “Said stock is held by the above named individuals, however, solely as nominees for the Bank voor Handel, Rotterdam, Holland, which is owned by one or more of the Thyssen family, nationals of Germany and Hungary. The 4,000 shares hereinbefore set out are therefore beneficially owned and help for the interests of enemy nationals, and are vestible by the APC,” according to the memo from the National Archives.

The Bush family was caught RED HANDED.

Jones recommended that the assets be liquidated for the benefit of the government, but instead UBC was maintained intact and eventually returned to the American shareholders after the war. Some claim that Bush sold his share in UBC after the war for $1.5m – a huge amount of money at the time – but there is no documentary evidence to support this claim. No further action was ever taken nor was the investigation continued, despite the fact UBC was caught red-handed operating a American shell company for the Thyssen family eight months after America had entered the war and that this was the bank that had partly financed Hitler’s rise to power.

The most sensational part of the story remains shrouded in mystery: the connection, if any, between Prescott Bush, Thyssen, Consolidated Silesian Steel Company (CSSC) and Auschwitz.

Thyssen’s partner in United Steel Works, which had coal mines and steel plants across the region, was Friedrich Flick, another steel magnate who also owned part of IG Farben, the powerful German chemical company.

Flick’s plants in Poland made heavy use of slave labor from the concentration camps in Poland. According to a New York Times article published in March 18 1934 Flick owned two-thirds of CSSC while “American interests” held the rest.

The US National Archive documents show that BBH’s involvement with CSSC was more than simply holding the shares in the mid-1930s. Bush’s friend and fellow “bonesman” Knight Woolley, another partner at BBH, wrote to Averill Harriman in January 1933 warning of problems with CSSC after the Poles started their drive to nationalize the plant. “The Consolidated Silesian Steel Company situation has become increasingly complicated, and I have accordingly brought in Sullivan and Cromwell, in order to be sure that our interests are protected,” wrote Knight. “After studying the situation Foster Dulles is insisting that their man in Berlin get into the picture and obtain the information which the directors here should have. You will recall that Foster is a director and he is particularly anxious to be certain that there is no liability attaching to the American directors.”

John Foster Dulles was the brother of Allen Dulles who JFK fired in 1961 after the Bay of Pigs.  Coincidence?

Continuing the history lesson:  But the ownership of the CSSC between 1939 when the Germans invaded Poland and 1942 when the US government vested UBC and SAC is not clear.

“SAC held coal mines and definitely owned CSSC between 1934 and 1935, but when SAC was vested there was no trace of CSSC. All concrete evidence of its ownership disappears after 1935 and there are only a few traces in 1938 and 1939,” says Eva Schweitzer, the journalist and author whose book, America and the Holocaust, was published in 2004.

Silesia was quickly made part of the German Reich after the invasion, but while Polish factories were seized by the Nazis, those belonging to the still neutral Americans (and some other nationals) were treated more carefully as Hitler was still hoping to persuade the US to at least sit out the war as a neutral country. Schweitzer says American interests were dealt with on a case-by-case basis. The Nazis bought some out, but not others.

The two Holocaust survivors suing the US government and the Bush family for a total of $40billon in compensation claim both materially benefited from Auschwitz slave labor during the second world war.

Kurt Julius Goldstein, 87, and Peter Gingold, 85, began a class action in America in 2001, but the case was thrown out by Judge Rosemary Collier on the grounds that the government cannot be held liable under the principle of “state sovereignty”.

Jan Lissmann, one of the lawyers for the survivors, said: “President Bush withdrew President Bill Clinton’s signature from the treaty [that founded the court] not only to protect Americans, but also to protect himself and his family.”

Lissmann argues that genocide-related cases are covered by international law, which does hold governments accountable for their actions. He claims the ruling was invalid as no hearing took place.

In their claims, Mr Goldstein and Mr Gingold, honorary chairman of the League of Anti-fascists, suggest the Americans were aware of what was happening at Auschwitz and should have bombed the camp.

The lawyers also filed a motion in The Hague asking for an opinion on whether state sovereignty is a valid reason for refusing to hear their case.

The petition to The Hague states: “From April 1944 on, the American Air Force could have destroyed the camp with air raids, as well as the railway bridges and railway lines from Hungary to Auschwitz. The murder of about 400,000 Hungarian Holocaust victims could have been prevented.”

The case is built around a January 22 1944 executive order signed by President Franklin Roosevelt calling on the government to take all measures to rescue the European Jews. The lawyers claim the order was ignored because of pressure brought by a group of big American companies, including BBH, where Prescott Bush was a director.

The US government and the Bush family denied all the claims against them.

In addition to Eva Schweitzer’s book, two other books were published in 2004-05 that raised the subject of Prescott S. Bush’s business history. The author of the second book, John Loftus, is a former US attorney who prosecuted Nazi war criminals in the 70s. At that time he lived in St Petersburg, Florida and earning his living as a security commentator for Fox News and ABC radio, Loftus worked on a novel which used some of the material he has uncovered on Bush. Loftus stressed that what Prescott Bush was involved in was just what many other American and British businessmen were doing at the time.

“You can’t blame Bush for what his grandfather did any more than you can blame Jack Kennedy for what his father did – bought Nazi stocks – but what is important is the cover-up, how it could have gone on so successfully for half a century, and does that have implications for us today?” he said.

Those implications lead right to the death of JFK and RFK Jr.

“This was the mechanism by which Hitler was funded to come to power, this was the mechanism by which the Third Reich’s defence industry was re-armed, this was the mechanism by which Nazi profits were repatriated back to the American owners, this was the mechanism by which investigations into the financial laundering of the Third Reich were blunted,” said Loftus, who is vice-chairman of the Holocaust Museum in St Petersburg.  The US Treasury and Senator Warren wants you to believe in 2023 that Bitcoin is used to launder money when it is clear that this blog is laying the case out why rehypothecation of money is the strong suit of the CIA and all the people affiliated with them.

“The Union Banking Corporation was a holding company for the Nazis, for Fritz Thyssen,” said Loftus. “At various times, the Bush family has tried to spin it, saying they were owned by a Dutch bank and it wasn’t until the Nazis took over Holland that they realized that now the Nazis controlled the apparent company and that is why the Bush supporters claim when the war was over they got their money back. Both the American Treasury investigations and the intelligence investigations in Europe completely bely that, it’s absolute horseshit. They always knew who the ultimate beneficiaries were.”

“There is no one left alive who could be prosecuted but they did get away with it,” said Loftus. “As a former federal prosecutor, I would make a case for Prescott S. Bush, his father-in-law (George Walker) and Averill Harriman [to be prosecuted] for giving aid and comfort to the enemy. They remained on the boards of these companies knowing that they were of financial benefit to the nation of Germany.”

Loftus said Prescott S. Bush must have been aware of what was happening in Germany at the time. “My take on him was that he was a not terribly successful in-law who did what Herbert Walker told him to. Walker and Harriman were the two evil geniuses, they didn’t care about the Nazis any more than they cared about their investments with the Bolsheviks.”

What is also at issue is how much money Bush made from his involvement. His supporters suggest that he had one token share. Loftus disputes this, citing sources in “the banking and intelligence communities” and suggesting that the Bush family, through George Herbert Walker and Prescott, got $1.5m out of the involvement. There is, however, no paper trail to this sum.

The third person going who went into print in the early 2000s on this subject is John Buchanan, 54, a Miami-based magazine journalist who started examining the files while working on a screenplay. In 2003, Buchanan published his findings in the venerable but small-circulation New Hampshire Gazette under the headline “Documents in National Archives Prove George Bush’s Grandfather Traded With the Nazis – Even After Pearl Harbor”. He expands on this in his book – Fixing America: Breaking the Stranglehold of Corporate Rule, Big Media and the Religious Right.

In the article, Buchanan, who has worked mainly in the trade and music press with a spell as a muckraking reporter in Miami, claimed that “the essential facts have appeared on the internet and in relatively obscure books but were dismissed by the media as propaganda and Bush family as undocumented diatribes”.

One of the USAs oldest Jewish publications, the Jewish Advocate, has aired the controversy in detail in print.  Review it at your leisure.

Please recall that President George W. Bush gave us the Patriot Act after “the emergency” of the Twin towers “happened”.  I no longer think the Twin Towers was a terrorist action. I believe Bush pulled a play out from his family blue print.

George H.W. Bush, George W. father, also served as Director of Central Intelligence (DCI) from January 1976 to January 1977, just ten days shy of one full year. Though his tenure was limited, his accomplishments were many, and we are grateful to have served under his leadership. He became president after Ronald Reagan.

There is the link to Big Oil families who had a hand in killing the 35th President of the USA.  MoMA’s John Hay Whitney and Thomas W. Braden were members of the OSS. The OSS became the CIA in 1947.  Never forget what this criminal cabal has done and continues to do.

Game, Set, and Match.

That is conclusion of the RFK Jr interview you did not hear and what i said live on stage in Lisbon, Portugal.

Happy Thanksgiving.

CITES

1.https://www.moma.org/momaorg/shared/pdfs/docs/press_archives/4562/releases/MOMA_1970_July-December_0082_133F.pdf

2. https://twitter.com/DrJackKruse/status/1727329402571067413

3. https://twitter.com/DrJackKruse/status/1727370879460376756

4. https://twitter.com/DrJackKruse/status/1727371695017558289

5. http://www.cambridgeclarion.org/press_cuttings/braden_20may1967.html

QUANTUM ENGINEERING #61: HOW DOES LIGHT CONTROL CONSCIOUSNESS?

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8G mimics a car wreck to the human brain or an NFL LB hit to a QBs head.  These situations induces brain trauma at a space time continuum.  Nothing yet I have said is ground breaking to group of neurosurgeons.  This post below is a groundbreaking mitochondrial medicine lesson.

Today’s lesson on biophysics of consciousness:

Light illuminates the reality of what time and space are to the human experience.  Time and space are mere illusions of our perceptual abilities.  If you use physical forces in Nature we can induce consciousness and we can make it disappear right before your eyes even as nothing on Earth really changes to prove this point.  How?  Watch the video.  Time & space are constructs used by humans to better understand and operate in our world. That there is no such thing as an “external” and “internal” world and what we think we see “out there” is literally occurring and being conceived inside our head at the ATPase level.

Based on physics and biology, this science is unfortunately reality; it turns out that our ability to handle to use sunlight to handle the atomic mass in our ATPase that allows us to be consciousness.  That sole ability that dictates all that we see and perceive in our world.

The colony of mitochondria in the human brain has a massive fleet of ATPase’s in it and the video above shows you how fast its physiology can be altered.  The sunlight in the video did not change.  The amount of deuterium in his head did not change.  But the velocity his body flet did change and that change altered how the nanorotors operates in his head.  He went from energy efficient to energy inefficient in a few seconds when the key environmental variables around light remained constant.  There is a deep lesson in biophysics here.

Proof that this counterintuitive idea is true?

This is time lapsed photography of what happens in neurodegeneration in older humans that over decades.  It does not have to take that long if the atomic mass is added at a faster rate in a younger brain.  This young brain experienced the increased mass via momentum of the force of gravity induced by velocity and not the weight associated with the atomic mass of deuterium.

Deuterium’s higher atomic mass effectively mimics the increase G forces in your ATPase and your brain fails under that weight or mass.  Consciousness declines to neurodegeneration and cognitive decline before your brain fails in death.

Anesthesia also induces this effect on our patients and we take it for granted and never study it.  Do you know that strong magnetic fields induce unconsciousness in living things?  Anesthesia induces dielectric and magnetic flux collapse.

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Decentralized medicine has answers that centralized medicine whiff’s on.

QUANTUM ENGINEERING #60: HOW DOES LIGHT CONTROL POMC CLEAVAGE?

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Most people know about single nucleotide polymorphisms (SNPs) or single amino acid polymorphisms (SAPs), but few people ever get told how they operate in health and disease.

N-acyl amino acids in humans can involve acetylation, and C-terminus amino acids can be involved with methylation.  Both are controlled by light.  This post describes how the process happens.

Modifying the C-terminus of proteins is essential in understanding what light is doing biophysically to determine what biochemistry is possible in a cell.  The C-terminus is also known as the carboxyl-terminus, carboxy-terminus, C-terminal tail, C-terminal end, or COOH-terminus.  It represents the end of an amino acid chain (protein or polypeptide), terminated by a free carboxyl group (-COOH). When the protein is translated from messenger RNA, it is created from the N-terminus to the C-terminus. The convention for writing peptide sequences is to put the C-terminal end on the right and write the sequence from N- to C-terminus.

For example, while the N-terminus of a protein often contains targeting signals, the C-terminus can include retention signals for protein sorting. The most common Endoplasmic Reticulum retention signal is the amino acid sequence -KDEL (Lys-Asp-Glu-Leu) or -HDEL (His-Asp-Glu-Leu) at the C-terminus. This keeps the protein in the endoplasmic reticulum and prevents it from entering the secretory pathway in a cell.

For example, when the skin over the gut with a massive amount of POMC is not stimulated by solar light, POMC is lightly translated, and Vitamin D levels stay low.  As a result, one form of C-terminal modification is prenylation. During prenylation, a farnesyl- or geranylgeranyl-isoprenoid membrane anchor is added to a cysteine residue near the C-terminus. Small molecular weight, membrane-bound G proteins are often modified this way.  The circadian mechanism in cells operates via G proteins. With proper solar light, prenylation goes smoothly.

The enterocytes in the gut form a barrier.  They include a mechanical boundary against pathogens, antigens, and toxins; the monolayer of intestinal epithelial cells (IECs) represents the human body’s largest contact area with the environment due to villi folding. From their early development in the crypt bottom until the shedding of aged cells at the villus tip, IECs follow a continuous turnover process. This process is controlled by the circadian mechanism in the SCN and transmitted to the gut via the peripheral nervous system and the melanin sheets in the organ of Zuckerlandl, where melanin and POMC reside.

Under physiological conditions, a complex interaction between cytoskeleton rearrangement and tight junction proteins guarantees that the cell shedding itself does not mean a disturbance of epithelial integrity. However, alterations of epithelial integrity lead to the development of gut inflammatory disorders, such as inflammatory bowel diseases (IBDs). IBDs are associated with marked alterations of IECs, leading to increased tight junction permeability, altered cytoskeletal rearrangement, and induction of epithelial cell death with a subsequent loss of barrier function.  All IBDs are linked to poor solar exposure and or artificial light at night on the skin or via the eyes.

In Crohn’s disease, there is Rho-A prenylation, and the absent solar light then changes protein signaling in the enterocytes of the gut.  This links epithelial homeostasis directly to intestinal inflammation.

The peptide created by POMC before cleavage is composed of three such segments: N-POMC, which is located at the N-terminus; ACTH, which is located in the middle; and β-LPH, which is located at the C-terminus. Each of these segments contains one MSH sequence: γ-MSH in N-POMC, α-MSH in ACTH, and β-MSH in β-LPH.

The N-terminus is also known as the amino-terminus, NH2-terminus, N-terminal end, or amine-terminus, is the start of a protein or polypeptide, referring to the free amine group (-NH2) located at the end of a polypeptide.  Look at the structure of melanin below when it interacts with an electrophile metal.

When a protein is translated from messenger RNA, it is created from the N-terminus to the C-terminus. The amino end of an amino acid (on a charged tRNA), during the elongation stage of translation, attaches to the carboxyl end of the growing chain. Since the start codon of the genetic code codes for ONLY one amino acid, methionine, most protein sequences start with a methionine (or, in bacteria, mitochondria, and chloroplasts, the modified version N-formylmethionine, fMet). I wrote a blog on that topic on Patreon.  You should have expected I told you this for a reason before the melanin story came out of my mitochondrial mist.  The circadian mechanism operates 100% of the time in a posttranslational fashion.  I laid out that case at the Palestra Health conference when I presented to several politicians and hedge fund managers who were present.  Some proteins are modified posttranslationally, for example, by cleavage from a protein precursor and therefore may have different amino acids at their N-terminus.  Light frequencies can change the N-terminus in proteins.

The N-terminus is the first part of the protein that exits the ribosome during protein biosynthesis. It often contains signal peptide sequences, “intracellular postal codes,” that direct the delivery of the protein to the proper organelle. The signal peptide is typically removed at the destination by a signal peptidase. The N-terminal amino acid of a protein is an essential determinant of its half-life.  This is how the ubiquitin system operates, and quantum mechanics raises or lessens the probability of the likelihood of a protein being degraded. This is called the N-end rule.

The N-terminal signal peptide is recognized by the signal recognition particle (SRP) and results in the targeting of the protein to the secretory pathway. In eukaryotic cells, these proteins are synthesized at the rough endoplasmic reticulum.   Protein N-termini can be modified co – or post-translationally. Modifications include the removal of initiator methionine (iMet) by aminopeptidases, attachment of small chemical groups such as acetyl, propionyl, and methyl, and the addition of membrane anchors, such as palmitoyl and myristoyl groups.  There are many other N-terminus modifications like methylation.  Light frequencies dictate how biochemistry unfolds.  

N-terminus modification is how many diseases begin with aberrant light choices.  Many pharmacological, genetic, and mechanistic studies in mammals have suggested that certain members of the N-acyl amino acids stimulate mitochondrial respiration and whole-body energy expenditure directly. Other complementary studies have also established roles for N-acyl amino acids in glucose homeostasis, adipogenesis, vascular tone, and bone homeostasis.  This explains thoroughly why POMC has the protein construction it does.

The N-POMC is located at the N-terminus ACTH, which is away from the N and C terminus because it is located in the middle of the protein.  This is a deep evolutionary clue about how mammals used ACTH to create sugar from light cleavage.  What should shock you is that each of these cleavage segments contains one MSH sequence: γ-MSH in N-POMC, α-MSH in ACTH, and β-MSH in β-LPH.  This tells you that light and dark are controlling the peptide’s cleavage.

Notably, the functional consequence and enzymatic regulation of each N-acyl amino acid in mammals highly depend on the structural properties of the fatty acid tail group and amino acid head group.

By integrating whole genome sequencing data with N-acyl amino acid levels, one can identify the EPIGENETIC determinants of N-acyl amino acid levels and cluster according to the amino acid head group.   For example, in mammalian heart disease, this is why CYP4F2 is associated with many human cardiometabolic disorders.  Centralized science has now identified the CYP4F2 locus as an epigenetic determinant of plasma N-oleoyl-leucine and N-oleoyl-phenylalanine levels in human plasma, as the papers below show. In experimental studies, it has now been demonstrated that CYP4F2-mediated hydroxylation of N-oleoyl-leucine and N-oleoyl-phenylalanine results in metabolic diversification and production of many previously unknown lipid metabolites in humans with varying characteristics of the fatty acid tail group, including several that structurally resemble fatty acid hydroxy fatty acids. These studies provide a structural framework for understanding the regulation and disease associations of N-acyl amino acids in humans and identify that the diversity of this lipid signaling family can be significantly expanded through CYP4F-mediated ω-hydroxylation.

Modern “centralized chemical biology” relies increasingly on protein chemistry, which ideally allows precise positioning of labels, cargoes, and post-translational modifications (PTMs) in the contexts of complex protein structures. The resulting modified proteins prove helpful in determining proper physiology and Big Pharma therapeutic applications.  They allow us to understand the decentralized cell by the probing and modulating function, as well as their tracking and (un)caging in cells that happen with light and dark cycles.

Big Pharma chemists have developed various methods to control the convergent construction of site-selectively modified proteins. Traditionally, the non-site-selective chemical modification of proteins has relied on the nucleophilicity of the side-chains of natural amino acid residues like lysine (Lys) and cysteine (Cys), as well as protein N-terminus through direct acylation, alkylation and arylation with a wide array of electrophiles.  In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair. Electrophiles accept electrons in biochemistry. Biological electrophiles are defined as electron-deficient species of chemicals that include heavy metals, environmental pollutants, toxic drug metabolites, flavor enhancers like Splenda, cell signaling mediators, and unsaturated aldehyde products of membrane lipid peroxidation.

When DHA is in the SN-2 position, it becomes planar. This is what turns the central retinal pathways of the retinohypothalamic tracts into a wide band gapped semiconductive LED array that targets melanin all over the brain. Melanin absorbs all light, ROS, and RNS to charge separate water to create a tremendous amount of electrons to power the system. In this illustration, electrons act as a canvas does in a painting: sunlight is the paint, and electrons are the brushes.

SUMMARY

BLUE LIGHT IS A STIMULANT THAT CREATES ROS/RNS NORMALLY

And stimulants are 👍 great. Most Americans drink a few cups of stimulants each morning ☕️ to get themselves up to face the daily grind.

But you know what’s not great? Being stimulated 24 hours of every day by blue light. This ruins the dose-response curve of the ROS/RNS. That is exactly what is occurring to modern humans because they live indoors and use tech screens excessively. What else is different about this version of blue light? The blue light that wakes us up in the sun is NEVER present without 42% IR-A light, which is red.  AM sunlight has 42% red light and only 1600K of blue light. This small stimulus of blue light is about to improve executive function of the prefrontal cortex. This blue light needs red light to control the oxidation ROS/RNS that blue light makes when present without red light in our light environment.

ALL CELLS contain ion channels in their outer (plasma) and inner (organelle) membranes. Ion channels, similar to other proteins, are targets of oxidative impact, which modulates ion fluxes across membranes. Subsequently, these ion currents affect electrical excitability, such as action potential discharge (in neurons, muscle, and receptor cells), alteration of the membrane resting potential, synaptic transmission, hormone secretion, muscle contraction, or coordination of the cell cycle.  Circadian biology controls all of this.

An important class of ion channels is the family of potassium (K+) channels (in the nitric oxide cycle); they are not only in charge of the membrane resting potential or the repolarization of the action potentials but also control cell proliferation or transmitter/hormone release, to name a few. A subgroup of K+ channels are the so-called calcium (Ca2+) activated K+ channels, which need either an increase of Ca2+ at their intracellular face to open or a combination of Ca2+ and voltage to function correctly. Maxi Ca2+-activated K+ channels, also named BK channels, constitute a subgroup of Ca2+-activated K+ channels.

Do you know where these ion channels exist in humans?  They are found on the inner mitochondrial membrane. EXCESSIVE BLUE LIGHT exposure destroys these potassium ion channels to ruin signaling of cells that control the circadian mechanism and are associated with leptin and melanopsin. LET THAT SINK IN with all the ways modification happens on the C and N terminus of proteins.  I only shared a couple with you in this blog.  

Mitochondria are a significant source of ROS generation targeting BK channels. Blue light creates that stimulus when RED LIGHT IS ABSENT.

The inner membrane of mitochondria contains BK channels (mtBK), which appear essential in the production of ROS. mtBK channels appear to be inserted into the mitochondrial membrane with the toxin binding sites for charybdotoxin and iberiotoxin exposed to the mitochondrial intermembrane space. This can be accessed using outside-out patch configuration of the inner mitochondrial membrane. Consequently, the C-terminal tail domain, including the Ca2+ binding site, is localized to the mitochondrial matrix where the proton gradient exists. 

RED LIGHT MOVES PROTONS BEST. Blue light creates the most ROS. Do you understand why subtracting red and UV light from blue creates mitochondrial diseases now?

Can you imagine what the centralized chemists controlled by Big Pharma may find when they look at C and N terminus modifications by light frequencies in POMC or DHA in humans?

CITES

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5. https://www.cell.com/cell-chemical-biology/abstract/S2451-9456(20)30146-X

6. https://pubmed.ncbi.nlm.nih.gov/26365347/

7. https://pubmed.ncbi.nlm.nih.gov/20136843/