Author: info@kruseatdestin.com

Fritz Popp earned a PhD in theoretical physics from the University of Mainz in 1969 and was awarded Professorship by the Senate of Marburg University. His work delved into quantum theory of many-particle systems and through his research is was able to prove the existence of “biophotons”.

WHY POPP NEVER COULD WRITE THIS BLOG SERIES EVEN THOUGH HE FOUND THE BIOPHOTONS STORY FIRST?

The reason is simple.  It was the same reason Max Plank could never explain the ultraviolet catastrophe but Einstein could.  Sir Albert looked at the thermodynamic givens, embraced their paradox, and knew nature does not make errors.  His mind went deeper into the complexity of light.  Planks gues right photons use quanta of light but he stopped there.

Popp did not understand wide band gaps because he was a theoretical physicist and not a theoretical biologist.

Popp got into biology from physics when he found out that cancer could only be linked to its optical properties and not its chemical properties.  From 1970-2018 to his death he never explained the situation.  I realized in 2005 I might have.  Let me explain.  In 1970, Fritz Popp discovered that benzo[a]pyrene, a potent carcinogen, absorbs ultraviolet light at one wavelength and emits it at another lower powered frequency of light.

He showed benzoapyrene, absorbed UV light and then re-emitted it at a different frequency (i.e. “scrambled” the light) while the latter molecule, benzoepyrene, allowed the UV light to pass through it unaltered. This told him that UV light signaling in cells was critical to get right and it required atomic precision in a cell.

The reason chemicals became carcinogenic was because their ability to enter mitosis was altered.  Popp never figured this out in all his experiments on chemicals, which is surprising.  It was clear however, he knew about Gurwitch’s experiments on mitogenic radiation from the 1923 onion experiments from his writings, but I do not think he knew enough about cell cycle biology.  I think he believe the paradigm beliefs that excess mitosis caused cancer.  The real answer was that mitosis is needed to avoid cancer.  When cells are arrested at the mitosis cell cycle this is when cells are optically sensitive to oncogenesis.

UV light frequencies are clearly needed for cells to navigate all the steps in the mitosis phase of the cell cycle.  So this should raise the question in your mind, where does this light come from?

WHAT DID POPP DO WITH THIS QUESTION?

This question led Dr. Popp to experiment with UV light and other compounds, some carcinogenic and some not. From his findings, Dr. Popp was able to predict which substances were carcinogenic by checking their specific optics – he observed that compounds that were carcinogenic would only react to light at a specific frequency (380 nm) by absorbing it and then re-emitting it at a different frequency.  In other words, carcinogenic chemicals could have identical chemical abilities but if they were “visible light scramblers” cancer would be the result.

The carcinogens seem to “scramble” the UV light signal with a wavelength of 380 nanometers. 380 nm light corresponds to a band gap of 3.25eV.  POMC responds ideally to the UV light 380 nm band gap.  380nm light also plays a huge role with mTOR biology and many other cellular processes (above).

This explained everything to me that Popp had found in his experiments.  I have not found one paper from Popp that mentioned POMC so I believe he had no idea that POMC was created from UV light in human tissues.  Without POMC there can be no melanin.  Without melanin the VUV light signals in tissues are lost and cells would be arrested at the mitosis stage of the cell cycle.  

The benign chemicals did not scramble the UV light signal but the cancerous ones did and this lowered the POMC in tissues where cancer came from while eroding their ability to make melanin.  The change in the UV signal emission caused the cells to stop their cell cycle at mitosis via optical scrambling.

This loss of signal fidelity allowed the cells to become mobile in tissues so they would find a new source of UV light where they could then grow.  This is how wound regeneration proceeds on in Becker’s experiments in salamanders.  Popp and Becker knew parts of this story, but neither of them could fully explain it.  I felt I could fully explain it because of the onion experiment of Gurwitsch and the KT event effect on melanin. There is one thing left to explain. Where do the biophotons come from?

 

BIOPHOTON TRANSFORMATION COMES FROM H+ LATTICE CHANGES IN THE MATRIX WITH 02 PRESENT

Time controls the flow of energy in matter.

Mitochondria are time machines who make their own ocean of water from visible light. They do not make energy, they transform it using atoms with a specific atomic arrangment in the organelle. When the organelle changes its size and shape it is a sign the time machine is a broken clock.

Energy transformation is not the sole function of mitochondria, since they have evolved as critical regulators of various cellular processes including metabolism, apoptosis, calcium buffering and cell division. The link to cell division is ANCIENT and why they should be thought more as a time machine and less as a powerhouse. Their reputation is misguided. Given that mitochondria cannot be formed de novo, it is important to gain deep insights into the molecular mechanisms governing the inheritance of preexisting organelles in each cell division in order to prevent mitochondrial damage and detrimental consequences on cell physiology. Their clock timing mechanism is critical in cell division which is a time critical event in a cell for an organism.

On Earth, in every living thing, the time of day determines the design of the mitochondrial network, and this, in turn, influences the cells’ energy capacity.”

Life uses the sun to tell cellular time. Relationship between circadian clock and energy production is not well understood by centralized medicine so I do not expect the public to understand it well either. New research shows that Life’s mitochondrial network loses its key rhythms if the circadian clock is impaired, which in turn, causes a decline in energy production in the cells.

The researchers showed that the circadian clock and mitochondria interact through a protein called the dynamin-related protein 1 (DRP1), a key mediator of mitochondrial fission. Specifically, they found that pharmacologically or genetically impairing the mitochondrial Drp1 fission protein upsets the energy production rhythm, which in turn affects the rhythm of the circadian clock leading to heteroplasmy changes and disease. This is how chronic diseases begin.

Mitochondrial fission and fusion cycles are integrated with cell cycle progression. A lack of ultraweak UV light is key in this process. Inhibiting Drp1 triggers DNA replication stress, which is mediated by a hyperfused mitochondrial structure and unscheduled expression of cyclin E in the G2 phase of the cell cycle. This persistent replication stress then induces an ATM-dependent activation of the G2 to M transition cell cycle checkpoint. Cells need ultraweak UV bio-photon creation to get past the Mitosis phase in the cell cycle.

At the G1/S boundary in the cell cycle mitochondrial tubules form a highly fused network, which is associated with increased mitochondrial ATP production (PBM effect) and high levels of cyclin E, in order to promote G1-to-S transition (Mitra et al., 2009).

This hyperfused mitochondrial network is then disassembled and becomes increasingly fragmented through S, G2 and M phase of the cell cycle, with the greatest fragmentation evident during mitosis (M) in order to allow the proper partitioning of mitochondria between two daughter cells during cytokinesis.

I now believe most modern diseases result from showing a regressive evolutionary path. This is called atavism. You heard that idea in this series already in QE #45. In my opinion, most modern diseases manifest by showing evidence of semiconductive proteins undergoing photolithographic engineering inside your tissues to change light frequencies, which alters your tissues’ water chemistry. This leads to new and alien bends, charges, and alteration of atoms in your tissues that change the morphology of your body and the physiology of your tissues. The most powerful changes occur in the POMC gene family and all the peptides it creates by light frequency cleavage. Changes in light frequency alter the dielectric potential in water, which sculpts semiconductive design. This is functionally how evolution occurs. It is not the path that Darwin put centralized science on.

My unconventional decentralized theory of atavism and photolithographic engineering goes against current mainstream scientific beliefs. However, It is plausible because of the science underpinning the solid-state physics that governs semiconduction and optics. While evolution plays a role in disease development, it is typically understood in centralized science via the lens of genetic mutations and natural selection = Darwinism The idea of light frequencies altering tissue chemistry and causing changes in the body is not well-supported by current centralized scientific evidence because no one in centralized science is allocating money to study it. BigHarma and the NIH are invested heavily in the belief that alterations of RNA and DNA are how evolution happens exclusively. They do not even allocate 1% of their funding to mtDNA studies. This shows you why decentralized action below the cell level remains hidden from the public. This blog will make you realize just how much they do not know and why we must question their authority on this topic. If you think there is no PEER reviewed literature supporting my belief that genes do not cause cancer look at the paper below from 2017.

MITOCHONDRIAL ELONGATION MIMICS GLOBE ELONGATION = DECREASED ENERGY

Thus, mitochondrial remodeling throughout the cell cycle is considered to meet the cellular energy demands during the progression of specific stages of the cell cycle, and to ensure faithful inheritance of mitochondria during cell division. However, how deficiencies in the proteins that regulate mitochondrial dynamics impact cell cycle progression and hence directly contribute to the development of diseases. Loss of Drp1 results in elongated mitochondria. Drp1 deficiency mimics what blue light does to the globe in myopia. It elongates the mitochondria. This causes mitochondrial dysfunction due to a failure of a Drp1-dependent mechanism of mitophagy that removes damaged mitochondria within the cell (Twig et al., 2008 = heteroplasmy).

When size and shape changes in mitochondria this changes the H+ lattices that are possible in the matrix. When an atomic crystalline latiice is changes they release light as a response. This idea is buried in the slide below.

The resulting accumulation of damaged mitochondria has been suggested to cause a depletion of cellular ATP and an inhibition of cell proliferation (Parone et al., 2008 TCA cycle spinning counterclockwise). Such an energy depletion-related cell proliferation defect may be caused by a metabolic checkpoint that triggers an AMPK- and p53-dependent G1/S cell cycle arrest (Jones et al., 2005; Owusu-Ansah et al., 2008). Persistent mitochondrial hyperfusion also induces centrosomal overamplification and chromosomal instability, which are causes of aneuploidy. p53 is a gene product that protects the genome, DRP1 inhibition is how you lose control of the nuclear genome. This is how DNA defects occur from mitochondrial peptide creation. = transgenerational epigenetics

 

KEY BLOG POINT: HOW BIOPHOTONS ARE MADE

Mitotic machinery transforms energy from matter (matrix H+ lattice changes from elongation) using oxygen and H+ to stimulate light release in the form of biophotons, which in turn, to regulate mitochondrial homeostasis.

Why is oxygen needed to make biophotons? You won’t find this answer in Roeland van Wijk’s book on this topic. You will find it here for 5 bucks. Oxygen is a powerful element for the human gut because of what it does to electrons. Oxygen use by life began the initial penetration of solving complexity in tissues and organizational structure. It being the only paramagnetic gas on the periodic table makes it pathway unique for information processing in a quantum cell. O2 has two unpaired electrons. Electrons are key parts of mass to run photons in tissues: see the photoelectric effect.

Tissue complexity is enabled by the number of electrons, and is responsible for producing more electrons in a thermodynamic system. This is why life exploded after the Cambrian event. There is no other reason. We need more electrons to get more oxygen so we can generate more electrons to carry light in the system. This is why humans lost their fur. Their skin became a new mode to recover more electrons from the sun, in the from of photons. Your skin is a solar panel for the complexity in your chest and brain.

Oxygen’s electrons are really more important to how humans work in decentralized fashion. For Example, if you have any skin disease (neuroectoderm derivative) that is associated with an altered immune response, do you know why the sun is your Rx for wellness? Did you know singlet oxygen is a potent trigger for the induction of human T cell apoptosis because of its electrons. Did you know UVA light from the sun is the most potent trigger to singlet oxygen production in the all neuroectodermal derivatives? Did you know melanin in the skin augments this effect because it is also a neuroectodermal tissue? I doubt you do because no centralized MD does.

Remember electrons and photons are basically the same thing with respect to how the photoelectric effect operates in the quantum realm (oversimplified obviously). They are the particle in Nature which has a way to capture a massless source of energy and information contained in light and move it by ionization or delocalization. This helps explains why all cells release ultraweak UV light. You should also realize that UV light creates oxygen in the atmosphere and in the venous side of your circulatory system. Big implications for chronic diseases when hypoxia is present in the system; it causes things to go awry.

Any replication stress then initiates the DNA damage response.

Proof: All living cells emit ELF-UV light and how we see how fluids and atoms are moved in cells = AMO physics 101.
https://www.eurekalert.org/news-releases/518737

More sunlight = more information in the system to build complexity = more oxygen
Time appears as entropy goes from order to disorder. When entropy is controlled by a dissipative system, time can appear to be illusory.
This means that the less information you have about a data set in a cell, the higher its entropy must be in the system. Cells limit entropy by controlling their atomic arrangements. In precise terms, entropy is a measure of the number of possible atomic arrangements that a system of particles can be in.This is important in understanding how Nature engineered our biological clock gene to work.

Remember that stored energy in HEALTHY cells is coherent energy. The organism is, therefore, a highly coherent domain possessing a full range of coherence times and coherence volumes of energy storage. This keeps it far from equilibrium and makes it a highly dissipative system of organization to control entropy.

Reminder: Cellular organization is the key to precision optical signaling. Life is all about optimizing AMO physics INSIDE OF CELLS. It transforms energy from the environment to do this. Modern physics now has proven that energy and information are equivalent in physics. Landauer’s Principle of 1961 & Shannon’s 1948 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 enzyme kinetics, membranes, and in gradients, fields and flow patterns, compartments, organelles, cell water, 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. It is energy on demand by atomic design.

 

 

SUMMARY

During his work with chemicals, Popp learned that 380 nanometers, the wavelength altered by carcinogens, is also the key wavelength that cells prefer to use to repair themselves. After exposure to intense UV light, cells quickly self-repaired themselves when they are exposed to very weak UV light, particularly that with a wavelength of 380 nanometers. Popp hypothesized that cancer results from a disruption of cells’ photo repair system. What he never seemed to realize was that 380nm is the frequency of the mitogenic radiation in Gurwitch’s onion experiment that restored mitosis in cells.

His hypothesis raised a question: what in the body produced this very weak light that powered the repair system? Popp and his student Bernard Ruth found that all living systems store light energy (photons) acquired from the sun and from plants consumed as food (photosynthesis), in DNA. This stored light is released as very weak, extremely coherent biophotons. UV light photons made from wide-band gapped semiconductors switch on the body’s processes like a conductor launching each individual instrument inside the cell.  This orchestration is how the products are cleaved from POMC in different tissues to lead to disease or wellness. It was the alteration of the band gap that was the key to optical control in a cell that led to “the collective sound” at different frequencies as they perform different functions.

Over the years, Popp found that biophoton emissions from healthy humans display rhythmic patterns. He never realized those patterns linked to circadian changes of the hydrogen bonding networks in water.  He also observed that the coherence of the light emissions, the intensity, and the rhythmic patterns varied in people with different illnesses.

For example, people with multiple sclerosis absorb too much of the wrong light and their photon emissions display too much order and this affects the opening and closing of the AQA 4 gates in the CNS/PNS.  

The change in frequency of light changes oxygen tensions in the cell and mitochondria and this changes the ROS/RNS signals and the light emission of the cell.  When the light emission is changed, migration of the glial cells can cause AQA4 gate malfunction.  

This can be mediated by the divalent atoms in the mitochondria of those semiconductive gates.  Moreover, they stop working properly moving water with each action potential.  nnEMF can change the band gap of a system in a cell just by changing the VGCC on the membrane with a specific frequency.  (see below)

The sun creates a different calcium signal in MS patients.  The paper above shows that nnEMF also carries the ability to change calcium and magnesium flows in mitochondria and this will alter the band gap in these organelles.  This will change the free radical signals, oxygen levels in mitochondria and ultimate change the light emission from cells.  If light emission is changed  in glial cells Multiple Sclerosis is the likely outcome if glial cells migrate away from the AQA4 gate.

Schwann cell precursors (SCPs) are glial progenitors, closely associated with developing nerves of the peripheral nervous system along which they migrate, sometimes long distances, throughout the body. SCPs are derived from neural crest cells (all contain melanin) that emigrate from the neural tube and migrate into the periphery. Accordingly, SCPs closely resemble neural crest stem cells but also have properties that are characteristic of immature Schwann cells.   In our adult form Schwan cells appear to have migratory ability like melanocytes and WBCs in our immune system.  I believe MS is an abnormal migration of neurons due to an altered VGCC’s in their mitochondria that leads to short circuits in the neurons.

ALS MIGHT ALSO BE A MIGRATORY NEURON DISEASES DUE TO A LOSS OF ENDOGENOUS UV SIGNALING

All spinal motor neurons derive from motor neuron progenitor cells, located in a restricted ventral region of the developing spinal cord.

During late gastrulation and neurulation, the developing spinal cord is called the neural tube, and is patterned into distinct progenitor domains. MNs are specified from progenitors in the ventral neural tube. Once specified, newly born MNs are further specified into columns, pools, and subtypes, forming a unique topography. From these columns and pools, axons reach out to their targets under varying guidance cues. All MNs are cholinergic cells which integrate with the motor control circuit, the sensory system, and their outlying targets to control movement.  Given the growing importance of the MN–glia interaction in a number of neurodegenerative diseases it is important to know that the initial specification of oligodendrocyte precursor cells (OPCs) share a common progenitor with MNs.  This implies that motor neurons could degenerate into oligodendroglia or even back into neuroepithelium where they come from in the embryo.

Motor neurons (MNs) are neurons located in the central nervous system (CNS) controlling a variety of downstream targets in muscles. There are two main types of MNs, (i) upper MNs that originate from the cerebral cortex and (ii) lower MNs that are located in the brainstem and spinal cord.  This explains why some forms of ALS is worse than others.

If the nnEMF changes anterior and posterior neural plate neuron migration signals might explain why ALS occurs when anterior motor horn cells disappear.   The anterior end of the neural tube will develop into the brain, and the posterior portion will become the spinal cord. The neural crest develops into peripheral structures. At this point, the early nervous system is a simple, hollow tube. It runs from the anterior end of the embryo to the posterior end.

In vertebrates, neuroepithelial cells give rise to the neural tube, which forms through two processes along the anterior-posterior (AP) axis. The first process is primary neurulation, which progresses through convergent extension, elevation, bending, and fusion of the neural plate, forming the rostral neural tube. By the end of primary neurulation, only the brain and anterior trunk structures of the spinal cord have formed. As the embryo develops, progressive addition of new neural progenitors (NPCs) is required at the posterior end of the spinal neural tube for neural tube elongation. The cells at the dorsal region of the tail bud aggregate and the tail bud ultimately undergoes cavitation, forming the caudal neural tube; this comprises the future caudal domain of the spinal cord, which is in continuity with the neural tube in the trunk derived from the primary neurulation

Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND) or Lou Gehrig’s disease, is a neurodegenerative disease that results in the progressive loss of motor neurons that control voluntary muscles in humans

Currently no one knows where these anterior horn cells go, but given the papers on Zebrafish out of Stonybrook University in New York I bet the motor horn cells have altered melanin biology in those cells and this leads to their migration somewhere else in the nervous system.  This would mimic what we see in melanosomes mentioned in Quantum Engineering #30.

Why do I say this?

Human bodies, like those of other vertebrates, form in a ‘head-to-tail’ direction during embryonic development. There is growing evidence that this process is fuelled in large part by a pool of proliferating cells called neuromesodermal progenitors (NMPs; reviewed in Henrique et al., 2015). These cells have been found in zebrafish, chick, mouse embryos, and in human embryos (Olivera-Martinez et al., 2012).

Moreover, they seem to produce both the neural tissue that makes the spinal cord and mesodermal tissues such as muscle and bone.

Vertebrate embryos establish their primary body axis in a conserved progressive fashion from the anterior to the posterior. ALS is a disease that is linked only to anterior motor horn cells.  During this process, a posteriorly localized neuromesodermal cell population called neuromesodermal progenitors (NMps) plays a critical role in contributing new cells to the spinal cord and mesoderm as the embryo elongates. Defects in neuromesodermal population development can cause severe disruptions to the formation of the body posterior to the head. Given their importance during development and their potential, some of which has already been realized, for revealing new methods of in vitro tissue generation, there is great interest in better understanding NMp biology.

The nervous system of vertebrates can be understood as a means of internal interconnection that enables multicellular animals to coordinate their different physiological activities and interact with their environment.  ALS presents a seeming paradox to centralized healthcare because only

Zebrafish research at Stonybrook University by

thmic patterns. Also, tumors emit high amounts of photons: an average of 300 [+ or -] 90 photons/cm per minute compared with normal tissue emits an average of 22 [+ or -] 6 photons/cm per minute.  Human cells that emit too much light seem to be a problem.  I do not currently believe the amount is the issue I believe the frequency is the problem and this stops the cell cycle in mitosis.  When this occurs oncogenesis begins.

Popp and colleagues at the International Institute of Biophysics discovered that surface tumors and tumors excised during surgery respond to remedies with changes in photon emissions. This helped me understand mammal metastasis at the KT event and what the real cause of melanoma is today.

CITES

https://www.cell.com/cell-metabolism/fulltext/S1550-4131(18)30063-9

https://journals.lww.com/oncology-times/fulltext/2019/01050/non_proliferative_cancer_cells___the_deadly_charge.5.aspx

https://elifesciences.org/articles/14830

Elisabeth Zieger, Michael Schubert. New Insights Into the Roles of Retinoic Acid Signaling in Nervous System Development and the Establishment of Neurotransmitter Systems. Int Rev Cell Mol Biol, pp.1-84, 2017. hal-02117372

https://threadreaderapp.com/thread/1636019966947348480.html

https://x.com/DrJackKruse/status/1795236535069008254

Hydrogen = H+. Deuterium = D. . It is the atomic chameleon. It is the first element on the periodic table. It is what our sun is mostly made from and burns most to make energy. It is the element found in greatest density inside of a mitochondria. This makes it an interesting study point for Einstein’s relativity and cosmology and QED. Mitochondria have a really small scale of action and this small-scale effects the idea of relativity which is based upon geometry. Without the scale of geometry gravity’s effect is lessened to a great degree. Hydrogen (H+) has the ability to be a metal when it loses its electron; this is what happens inside our mitochondrial matrix. As H+ is can act a superconductor. Superconductors have special crystalline lattice and when that lattice is deformed it releases light. This makes it the focus of quantum electrodynamic theory. This means our mitochondria is filled with ionized plasma. This is very similar to what the sun does when it burns hydrogen. Hydrogen can be non metal when it has its electron orbiting its sole proton; It is also can be an acid because H+ is the basis of pH scale which measures acidity. Deuterium and a proton, have separate abilities and chemistry that varies. They both show up differently in MRI scans because of the differences in their physics. H+ and D interacts with water differently. H+ has the ability to do some unexpected things because of its ability to proton tunnel. The barrier for deuterium to tunnel is markedly reduced compared to H+. When we add infrared light H+ really become quite special. With 1538.5 nm photon frequency added to cell water, proton transfers in water are increased dramatically. This is called proton tunneling. This effect changes receptor biology and enzymes. Did you know every biologic enzyme known to man uses proton tunneling to work? All DNA and RNA only work when they are hydrated because they require hydrogen protons to tunnel!!! This makes hydrogen life’s magic weapon in enzyme and receptor actions. It has the same effect on DNA and RNA as well. Enzymes are 100% quantum experiments in energy and information transmutation. So how does hydrogen fit both Relativity and QED theory? Read on……………………..https://nautil.us/will-quantum-mechanics-swallow-relativity-235658/

 

The living universe selects for maximum entropy, and minimum waste heat.

The implications of this idea include:

The emergence of complexity: The universe’s drive for maximum entropy and minimum waste heat led to the melanin renovation Rx. This led to the emergence of complex structures and patterns, for life on Earth. Complexity came from becoming able to using the TCA in counterclockwise wise spin (anaerobic old system) and the clockwise wise spin (aerobic new oxygen Earth) during the same lifespan. New software patterns, like moving melanin to the mammalian interiors to begin to use endogenosus melanin to control the spin cycle of the TCA had to be innovated.

The arrow of time: The universe’s tendency towards increasing entropy explains why the human brain uses dopamine and melatonin as clock gear proxies. Both are critical in renovating all non visual photoreceptors in us. There use is why we perceive time as moving in a particular direction. Mammals’ criticality begins with UV light because it works with mtDNA, quantum dots, and melanin to create VUV-IR light inside a cell. When the critical amount of these entities goes missing inside mammals, they suffer a loss of healthspan or a loss of time.

The nature of consciousness: The self-organizing nature of the universe has massive implications for our understanding of consciousness and the human experience. The nature of consciousness is buried in the queerness of water’s abilities and what ultraweak biophoton spectral frequency change can do to steer water in its holographic format. Scientists at the US Department of Energy Oak Ridge National Laboratory (ORNL) have discovered new properties of water that go beyond the known laws of classical physics.

https://x.com/DrJackKruse/status/1776818496032153937

 

Fact: Blue light/nnEMF dehydrates cells because they stop H2O production from the mitochondrial TCA cycle. Why is this a big deal? Neurons absorb and release water when firing information. When H2O is MIA so are neurological function/capabilities. You lose the ability to sleep and account for time in your molecular clocks when water is absent. This is why children experience time differently than adults. Less water, less sunlight, or more ALAN at night destroy the clock timing mechanism of living things. Few see this recipe in life’s blueprint

You have to remember Vitamin D is a proxy for your time machine mechanism buried inside your mitochondria.  Your job is to see Nature’s science, then understand what it means for your longevity when you are sick.  This is a huge big deal if you complied and got jabbed. Without electrification of the phospolipids in your membranes you are asking for a jab complication.

Every person has a different efficiency rate of their time machines based on how the mechanism is built to operate.  Few see that Vitamin D is just a bystander in how the process works and this is why when your Vitamin D comes back is a very complex answer.

Here is how it operates.

Did you know the molecule of “more time” (melatonin) acts to aggregate melanosomes in cells to organize them magnetically at night when light is absent?

Did you know the molecule of “more time” optimizes another time crystal in mitochondria called tryptophan in NAD+ tell mitochondria where the Earth is in relation to the sun in a calender year to “fact check” seasonal light variations?

The non visual photoreceptor system in the skin integument, like cholesterols/melanin,  concern themselves with the powerful UVB sunlight to create vitamin D as a bystander chemical that acts to electrify the membranes of mammals.  This allows for carbon fixation as the top line in the slide shows. Different domains of life use timing and genes to change where energy flows. For example, plants have their own particular route of  carbon fixation, converting inorganic carbon  in carbon dioxide into organic compounds. They use sunlight to do it. Sunlight is turned into a DC electric signal in its membranes to store energy at the electronic level.  Carbon is primarily fixed through photosynthesis, but some organisms use chemosynthesis in the absence of sunlight. Mammals do this. They use their livers to replace the sun. The fixation of carbon dioxide into the skeletal muscle glycogen in intact fasted mammals is best explained by electrification of their membranes which leads to secondary deposition of glucose in the muscle supplied primarily by the liver. We know this by isotopic labeling.

THE ELECTRIFICATION OF MAMMALIAN CELL MEMBRANES IS DONE BY SUNLIGHT.

The sun light is turned into a DC electric signal which turns on the biosynethic decision making abilities in cells.  The phtonic skin signal informs the liver and kidney what to do with cholesterol and Vitamin D from this point.  The wisdom in your body should amaze you.

Did you know the that the molecule of “more time”, melatonin,  also controls the only two programs that recycle your mitochondrial engines, autophagy & apoptosis?   Go look two pictures above. It is right there on the bottom of the slide. Without melatonin creation by mtDNA, the quality control mechanism in mt DNA manifest in your heteroplasmy rate.  That rate becomes your healthspan and your possible longevity in your life.  This is why sunlight links to longevity. That is why the slide below exists.

The efficiency of your mitochondrial “time machines” links to ROS/RNS production from mitochondrial metabolism, which in turn, controls all the magnetochemistry that controls how timing inside of cell directs the flow energy in your key metabolic pathways. Timing alone, controls the decision tree in cells that says, “should this tissue use beta-oxidation, glycolysis, gluconeogenesis, the PPP to get the job of living in this environment.

Melanin, also made from UV A,B,C light controls the levels of ROS/RNS that is coming out of the mitochondria in cells. This is a UNIQUE signal (Kruse for Dummies idea).  Melatonin, Melanin, and Vitamin D and NO all manifest from UV light’s interactions with matter in your cells.

Darkness at night, due to the absence of light, cools cells so that magnetic effects in melatonin can use second messengers in cAMP and Ca2+ to aggregate melansomes located around your mitochondria to do its magics inside of cells to tell time to control energy flows.  You can fixate carbon and nitrogen at night using the energy stored in biomolecules in your liver to run the dark program without light.

For light to have its full biological effect, photons must be absorbed by visual and non visual photoreceptors in the living body.  If one or both are missing, there is no effect. ROS/RNS creation in mitochondria and left over oxygen from metabolism begin this timing process.

Superoxide and H202 are a type of ROS made in mitochondria when we are healthy.  Melanin keeps both in check. When do we make ROS during the day?  When the sun is out.  This is when cells also make melanin.  It is also when Vitamin D has an opportunity to be made as well.

BUT WHAT IF YOUR VITAMIN D DOES NOT RESPOND TO SUNLIGHT?

WHY BEING IN THE SUN & still having a low D3 level & STILL BEING SICK TELLS ME YOU GOT A VITAMIN A/nnEMF PROBLEM?

You know Vitamin D is yoked to Vitamin A right. I’ve only said it 1000 times in blogs and podcasts. So when you live in the sun and Vitamin D does not rise here is why——-> https://lnkd.in/e6zptMZW

Non native EMF destroys your clock timing mechanism in your cells and you lose the ability to control the flow of energy in cells. Disease results and you lose time and longevity. That is the story of life in a few words.

Now that the story ion timing is complete, you can see that any kind of blue light or non-native EMF basically uncouple vitamin A from melanopsin. That released retinol from the non visual photoreceptors destroys dopamine, melatonin, melanin, and all heme based photoreceptors so that light becomes useless to cells. This is why a low Vitamin D level is possible with a tan integument or a fit looking body. It does not mean your healthy. Without proper timing longevity is impossible. There is a reason this pictured is my pinned Tweet on X.

Blue light and nnEMF becomes a nuclear weapon for all photo receptors. So you’ll be interested in this. “You may not know it, B12 is a photoreceptor in humans. B12 is another non visual photoreceptor in the liver, CNS, and circulatory system.

And guess what happens when you have melanopsin and retinol damage to B12 levels? That’s the reason why vegans have such demolished B12 level and shrinks their brains and destroys their non visual photoreceptors everywhere, including MELANIN. When melanin goes, timing inside a cell is lost. Magnetochemistry in mammals controls how energy flows. It also controls periodicity in the clock genes and makes the job of the SCN easy. When this goes awry the SCN mechanism becomes uber important to control the molecular clocks in the mitochondria of tissues.

Daylight is always associated with higher electric fields and lower magnetic fields and this correlates to mornings having higher ROS production and melanin production.  It is not always linked to Vitamin D levels because UVB light is highly variable based on your latitude and light stability.   This effect is seen in mitochondria and it helps tan your interior.

THE TIME CRYSTAL BURIED IN CYTOCHROME 1 IS MADE OF TRYPTOPHAN IS NAD+ THAT LINKS TO MELATONIN BIOLOGY

The morning AM ROS burst at cytochrome 1 (NAD+/NADH) links to the PER2 gene in the mammalian clock mechanism to begin to measure entropy in cells. These effects are rooted in the spin selected ROS partitioning between the free radicals created from metabolism, superoxide and H202, known as the radical triad/pair mechanism of quantum mechanics.

SUMMARY

Energy is trapped directly at the electronic level in cells. Energy is stored as vibrational & electronic bond energies in biochemicals (PER/HIF-1), but also in the structure of the system: its membranes, and in gradients, fields and flow patterns, compartments, organelles & cell water and tissues only gain their organization behind their QED magic. That magic is done in how time controls the flow of energy in clock genes. Just wearing sunglasses does this. This is why people who wear sunglasses burn so often. It is an issue of timing and a loss of magnetochemistry.

Clock genes and time crystalline proteins that ticked when they absorbed light in some way were used to coordinate all zip codes inside the Jacquard cards of biochemistry in cells to measure the entropy to control the overall flow of energy in metabolic pathways. Time controls the flow of energy in matter and this allows cells to extract information about where the Earth is in relation to the sun. The sun created the most powerful protein in Earth’s history (melanin) because it can harvest the entire power potential buried in the electromagnetic spectrum.  When melanin is heated up it becomes a supreme electrical conductor. When it cools it mimics what a superconductor can do with magnetic flux in light. This allows for electron- electron interactions and for electron-phonon coupling only seen in superconductors. Yes, we have superconductive proteins in us that operate with light, temperature, and precision timing.

Water was the plasma for most of Earth’s history, but nature created melanin to work with water something unique occurred.  The binary code of life that builds order from chaos begins by deciphering the code that exists between H+ and deuterium separated from water and plugged into ancient biochemical pathways to sculpt something new.

Ocular and integumentary melatonin levels both end in leptin biology.  This is why the leptin receptor sits behind the retina and infront of the hypothalamus that controls energy balance. It also explains why our subcutaneous fat sits just below the skin, and why leptin, the hormone that links to the leptin receptor in the brain visits the brain every night during the dark, in the hypothalamus to adjust the clock timing mechanism in the SCN. Few see Nature’s recipes.  Hopefully some of you can start putting the science of the blogs together like a QUILT.

Cellular disorganization is always linked to poor timing and its effects always manifests in disease creation before death manifests; Disease and death are an immutable ledger built as a consequence of how time does or does not flow in our clock timing mechanisms in cells. In this way, we always seem to get the sense that illness comes before death in most living sequences unless we are talking acute trauma. This points out why the information of the organization is as important as energy flux in a cell to maintain wellness. Timing is the MOST critical ingredient in Nature’s recipes.

When timing is off inside of a cell, the energy cost become prohibitive for a cell in a diseased person whose tissues are afflicted with defective mitochondrial DNA. This amplifies the need for precision accuracy, and when that periodicity is absent, this amplifies the creation of new mutations in the mitochondrial genome. This further lowers energy production and this further magneifies timing efficiency and forms a doom loop for the cell. The phenotype in the cell when timing is lost is the alteration of epigenetic signaling mandating for higher turnover. Mitochondria mutations speed up nuclear genome action. When the nuclear genome increases it is for one reason: To fix the atomic arrangement of atoms inside of a cell to recapture the timing mechanism required for living. The nuclear genome is designed by nature to be quite stable and quiescient.

Mitochondrial DNA is more vulnerable to alteration than nuclear DNA, for two reasons.

First, mitochondria are a major source of intracellular reactive oxygen species (ROS). Therefore mitochondrial DNA is designed to be under much stronger oxidative stress than is the nuclear DNA.

Second, mitochondria have a matrix-side negative membrane potential to carry out oxidative phosphorylation. This electric membrane potential concentrates lipophilic cations inside mitochondria up to approximately 1,000-fold.

That electric potential called redox power is created by the trsansformation of sunlight. This is how light controls metabolism. Light > Food always. It is axiomatic.

 

CITES

https://www.nih.gov/news-events/news-releases/neurons-absorb-release-water-when-firing-nih-study-suggests

https://x.com/DrJackKruse/status/1613309435073413121

https://journals.aps.org/prb/abstract/10.1103/PhysRevB.109.245132

How do eukaryotic cells make light from matter? It all begins with the fact that oxygen is the terminal electron acceptor for eukaryotes mitochindria. The oxygen molecule O2 displays some very particular features. It is a paramagnetic gas. It is the second most electronegative element in the periodic table. Because of this one should expect that O2 is a very reactive chemical compound. Counterintuitively, however, it is a quite unreactive molecule on Earth. How can I say this? . A testimony to this is the decentralized fact that we live in a planet with a 21% oxygen atmospheric content, and nevertheless life thrives and even depends on it.

The reason why O2 is so much unreactive than we expect this atom to be, in spite of its electronegativity, is the fact that in the fundamental state it assumes a triplet electronic configuration. Triplet electronic configuration occurs when the valence electrons arrange in the O2 molecule has the electronic configuration with the least energy. According to the molecular orbital theory, this arrangement has a triplet character. Triplet character occurs when the two outermost electrons in oxygen have different antibonding orbitals, but with the same spin state.

3^O2 expresses the triplet character of the ground state. This ground state has a biradical chemical character, which renders it quite unreactive to most chemical compounds. This triplet character of oxygen makes ground state O2 a paramagnetic compound, where oxygen gas tends to move to the point of strongest magnetic field. This is why oxygen is drawn to your colonies of mitochondria. Mitochondria create a magnetic field because they have electron movements along its innermitochondrial membrane while having a spinning ATPase on that same membrane. This makes all mitochondrial respiation electromagnetic at the most fundmental level.

Implications of this for cells? The cell cycle is controlled by light creation in cells.

The metabolic rate in our mitochondria drives developmental timing by controlling the cell cycle.

Having light stored at the electronic level is critical to the mystery of morphogenesis.

Back at the origin of life 3.8 billion years ago on Earth electric membranes drove CO2 fixation by converting gases from volcanoes (driven by the solar plasma) into organic chemicals to create growth in the absence of oxygen. This was the first step life took at the ocean floors.

Metabolism has always been spontaneous on Earth. Today, we believe complex life emerged from ancient autotrophic pathways fueled by volcanic gases as carbon and the sun as ultimate energy sources. Variants of these pathways remain in modern autotrophs in the deepest branches of the tree of life. In this way, the DC electric current in membranes preceded all chemistry. The energy metabolism of modern autotrophs resembles the geological interactions of H2 and CO2 gases in hydrothermal vents. Centralized science believes this points to a metabolic origin of biochemistry at the interface of the lithosphere and hydrosphere. Decentralized science believes this points to a quantum thermodynamics at the core of life because the sun drives all these processes. This step is fundamentally why light tops food in all my discussions.

Reactive oxygen species (ROS) are formed during normal metabolic processes. Mitochondrial respiration is spontaneous on Earth. Genes amplify metabolism and in this way, gene products are capable of making more or less light from how they amplify or de-amplify metabolic networks in cells.

ROS are magnetic signal created from excess oxygen in mtDNA. People forget molecular oxygen is the only paramagnetic gas on the periodic table. This makes it a unique magnetic signal used in cellular communication. All free radicals have one unpaired electron to make them magnetic sugnals. All ROS are called singlet oxygen signals that come from mtDNA actions. When electrons are added to a magnetic molecule this is called a reduction type of reaction. When singlet oxygen is reduced by the addition of electrons, the ROS magnetic signal shifts to a lower energy state and as a result emits photon.

The electronic transition of electronically excited species from the singlet or the triplet excited state to the ground state is accompanied by photon emission. This is how light is crerated by life. In this mechanism only a few photons are emitted per second per square centimeter, the photon emission is ultra-weak in nature. But it is these photons that explain how light sculpts life.

Reactive oxygen species are formed during the metabolic processes linked to life-sustaining enzyme-catalyzing reactions. They also can be formed during the response to stress reactions when any life form is exposed to biotic and abiotic stress factors from our environment. When ROS are effectively scavenged by the antioxidant defense system, the oxidative effect of ROS on biomolecules such as lipids, proteins and nucleic acids is fully prevented.

HOW IS ENDOGENOUS LIGHT CREATED?

Cells cannot product light without oxygen or ROS/RNS made in mitochondria. Mitochondria are not only time machones, they are factoried for biophotons. That is the bare minimum and is confirmed in Roeland Van Wijk book on the topic of biophotons. During the process of cellular respiration, electrons are transported through a series of mitochondrial complexes to the terminal electron acceptor, molecular oxygen (O2). In the process of cellular metabolism, the electrons released from the ETC react with O2 to produce superoxide (O−2) radicals. Mitochondrial complexes I, II, and III contribute to the maximum in redox signaling. Superoxide radicals generated at complexes I and III are released into the intermembrane space which comprises 80% of superoxide radicals generated in the mitochondria and remaining 20% are made by mitochondrial matrix.  The mitochondrial permeability transition pore in the outer membrane of the mitochondrion allows the passage of superoxide radicals into the cytoplasm where it is dismutated to hydrogen peroxide, a highly diffusible secondary messenger. This reaction is catalyzed by superoxide dismutase located in the mitochondrial matrix (MnSOD) or in the cytosol (by Cu/ZnSOD).

Furthermore, aquaporin 8 serves a channel for the release of hydrogen peroxide from the cell membranes.  There is an another major site for the generation of ROS termed as peroxisomes where superoxide and H2O2 are generated through xanthine oxidase in the peroxisomal matrix and membranes. Other sources of ROS include endogenous metabolites such as fatty acids, prostaglandins, and exogenous components including drugs, flavorings, coloring agents, antioxidants, etc. These substances are processed in the smooth endoplasmic reticulum and transformed into free radicals, especially ·OH. Macrophages and leucocytes, as a part of immune response contribute to the formation of free radicals

SO NOW YOU KNOW HOW ROS ARE MADE, HOW DO THEY TRANSFORM MATTER TO EMIT LIGHT?

However, under circumstance, when the formation of ROS exceeds the capacity of antioxidant defense system, biomolecules in cells spins are changed by magnetic forces in mitochondria. The single unpaired electron of ROS oxidizes lipids, proteins in both nuclear genome and mitochondrial nucleic acids. This interaction leads to the formation of high-energy intermediates like singlet oxygen. The decomposition of high-energy intermediates generates the electronically excited species which undergo an electronic transition from either the singlet or the triplet excited state to the singlet ground state. When there is an electronic transition of electron spin light is liberated.

When electron spin is changed, & our biomolecules are changed and the result in matter in our cells is to liberate light.

Singlet oxygen, systematically named dioxygen and dioxidene, is a gaseous chemical with the formula O=O, which is in a quantum state where all electrons are spin paired. It is kinetically unstable at ambient temperature in cells, and its rate of decay is slow.

Singlet oxygen (represented as 1ΔgO2, abbreviated as 1O2 in papers) is not a radical but represents an excited state of O2 in which the spin of one of the unpaired electrons is changed to yield two electrons with opposite spins. The terms ‘singlet oxygen’ and ‘triplet oxygen’ derive from each form’s number of electron spins. The singlet has only one possible arrangement of electron spins with a total quantum spin state of 0, while the triplet state has three possible arrangements of electron spins with a total quantum spin of 1, corresponding to three degenerate states. An excellent way to detect the presence of singlet oxygen in reactions is using steady-state or time-resolved measurements to find its characteristic phosphorescence at around 1270 nm.

When oxygen is reduced by losing an electron, singlet oxygen is created chemically. Singlet oxygen is an reactive oxygen species (ROS). The loss of the electron shifts the biomolecule to a lower energy state and as a result it emits photon. RNS works exactly the same way. This is how mitochondrion make light from matter.

The oxidation of biomolecules occurs by hydrogen abstraction by superoxide anion and hydroxyl radicals or by the cycloaddition of singlet oxygen initiate a cascade of oxidative reactions that lead to the formation of electronically excited species such as triplet excited carbonyl, excited pigments and singlet oxygen. The abstraction of hydrogen is defined by the removal of a hydrogen atom or group from a molecule by a free radical. Hydrogen/deuterium atom abstraction is often confused with deprotonation, which is the removal of a hydrogen atom (i.e., a proton) by a base in an acid-base (proton transfer) reaction.

When deuterium is abstracted out by light cells need to use more UV light to do so because you need more VUV-UVC-UVB-UVA light to abstracted the heavier isotope of hydrogen because of the extra neutron. Generally, the way oocyte selection occurs in mammals is by hydrogen abstraction. The oocytes with the lowest atomic mass are ejected first. during menarche. As time elapses, the eggs with the most deuterium and released last because more light is needed to get that job done. This drains the electronic level of its stored light.

This means the older a pregnancy becomes the more light is needed in the transgenerational process. In this way you can see now why high maternal age and transgenerational epigenetic diseases occur. It is also why more chromosomal abnormalities occur as mammals age. If the UV light is expended abstracting deuterium there is less light left at the elctronic level to drive the cell cycle past the mitosis level. This is a huge problem in infertility, cancer, and in morphogenesis (autism)

The photon emission of these electronically excited species is in the following regions of the spectrum (1) triplet excited carbonyl in the near UVA and blue–green areas (350–550 nm), (2) singlet and triplet excited pigments in the green–red (550–750 nm) and red-near IR (750–1000 nm) areas, respectively and (3) singlet oxygen in the red (634 and 703 nm) and near IR (1270 nm) areas. The understanding of the role of ROS in photon emission allows us to use the spontaneous and stress-induced ultra-weak photon emission as a non-invasive tool for monitoring of the oxidative metabolic processes and the oxidative stress reactions in biological systems in vivo, respectively.

Transcriptional regulation of proteins is done by GLUT expression by ROS in cells.

Since ROS is made from excess dissolved oxygen not used in mitochondria, when oxygen in cells decreases, ROS signaling becomes more unique because of scarcity. This should make you think about my Kruse for Dummies lecture.

Low oxygen triggers signal-transduction pathways involved in both cell death and survival. Anoxia activates proapoptotic BCL-2 proteins and caspases to initiate apoptosis. The adaptive cellular events that occur in response to hypoxia are mediated largely by the transcription factor hypoxia-inducible factor-1 (HIF-1)

During hypoxia, ROS levels increase by design and play an important role in HIF-1α stabilization. HIF-1 consists of two subunits, HIF-1α and HIF-1β. Under normoxic conditions, prolines within the oxygen-dependent degradation domains (ODDs) of HIF-1α are hydroxylated by prolyl-4-hydroxylases (PHDs; Ivan et al. 2001). This hydroxylation mechanism acts as an ubiquitination signal leading to proteasomal degradation of HIF-1α. In the absence of oxygen, HIF-1α ubiquitinylation is inhibited allowing its interaction with HIF-1β to drive transcription of various target genes, including GLUT1. This is the basis of how the Warburg shift occurs in humans.

Stimulation of cellular glucose uptake in mammalian cells is frequently observed during conditions of oxidative stress when ROS and RNS spikes. GLUT1 helps in the transport of glucose, galactose, mannose, glucosamine and ascorbic acid in mammals.

HIF-1 induces the expression of multiple antiapoptotic BCL-2 proteins to promote cell survival. Interestingly hypoxia increases production of mitochondrial reactive oxygen species (ROS), which serve as signaling molecules to activate HIF-1.

Hypoxia-inducible factors (HIFs), are major molecules that respond to hypoxia and elevated temperatures to play important roles in cancer development by participating in multiple processes. HIF1 is linked to circadian clock controls, metabolism, proliferation, and angiogenesis. The Warburg phenomenon reflects a pseudo-hypoxic state that activates HIF-1α. In addition, a product of the Warburg effect, lactate, also induces HIF-1α. However, Warburg proposed that aerobic glycolysis occurs due to a defect in mitochondria. I believe the defect occurs, first, in the circadian mechanism to affect mitochondrial metabolism. Moreover, both HIFs and mitochondrial dysfunction can lead to complex reprogramming of energy metabolism, including reduced mitochondrial oxidative metabolism, increased glucose uptake, and enhanced anaerobic glycolysis

HOW DOES HYPOXIA LINK TO ALTERED TIME STAMPING IN CELLS?

Circadian clocks are endogenous coordinators of the 24-hour rhythm of behavioral and molecular processes in living organisms. For humans, a master clock modulating circadian rhythms is located in the suprachiasmatic nucleus of the hypothalamus and is a pacemaker of the system. In mammals, the circadian clock is comprised of a set of genes, which function as activators—CLOCK and BMAL, which, similarly to HIF, are bHLH-PAS transcription factors.

HIF-1α GENE HAS A TRANSCRIPTION REGULATORY ELEMENT TO ALTER THE CIRCAIDAN CLOCK MECHANISMS. THIS IS HOW DIESESE ARE CAUSED IN THE MODERN WORLD.

Through binding to regulatory elements containing E-boxes (also present in HIF-1α gene) they activate the transcription of repressor protein period (PER) and cryptochrome (CRY). Additionally, HIF can bind to promoter regions of repressor proteins through hypoxia response elements (HRE), causing their transcrioptional upregulation leading to altered cell signaling. This is how the redox shift leads to alien light creation to lead to genetic changes we see in ALL CANCERS.

It is believed in centralized science that mitchondrial ROS oxidizes lipids, proteins and nucleic acids and thus initiate a cascade reactions that leads to the formation of electronically excited species responsible for the photon emission in near UVA, visible and near IR regions of the spectrum. I think this is a simple explanation for what is really going at the atomic level in a cell.

To make it crystal clear how bad the advice centralized medicine is giving patients you just need to review this thread in the context of what is being clearly laid out in this blog. Read this thread below in blue before going on.

https://threadreaderapp.com/thread/1754147699799040292

COVID AMPLIFIES THIS SCIENCE FOR THE SLEEPING SO THEY WAKE UP WHERE MODERN DISEASES COME FROM

TURBO CANCERS, mRNA, SV40, CIRCADIAN MISMATCH LINKS TO BIOPHOTONS

p53 is an important tumor suppressor gene, found to be mutated or absent in over 50% of all cancers studied. It functions as a sequence-specific DNA-binding transcription factor. In response to double-stranded DNA breaks, p53 is converted from a latent to an active form. This results in increased expression of p53-responsive proteins such as p21 which are required for growth arrest at the G1-to-S phase transition. It also mediates apoptosis via the increased expression of proteins such as Bax. Inactivation of p53, therefore, results in the loss of a cell cycle checkpoint control required for repair of damaged DNA and prevents apoptosis in response to severe DNA damage. In the absence of these responses, oncogenic mutations which may result in tumor progression can accumulate in nuclear DNA and this can happen quickly in people who took the mRNA jab. The damage can accumulate rapidly. From the above, it is clear that the transcriptional activation function of p53 is critical to its role as a tumor suppressor gene. Since genes amplify metabolic networks, p53 clearly clearly has a lot to do with the biophoton spectra that cells emit.

Note the history of the discovery of p53 brings us back to the story of SV40 and the polio vaccine. That is why Pfizer erased it from their plasmid map in the mRNA platform.  Simian virus 40 (SV40) large tumor antigen (T antigen) has been shown to inhibit p53-dependent transcription by preventing p53 from binding to its cognate cis element.

Why is p53 called p53?

One must know the history and the discovery of the most studied gene in human history, also known as the guardian of the genome.  Why is it considered the guardian of the genome?  Aneuploidy refers to the state of unequal chromosome copy numbers and is one of the most prominent genomic aberrations in solid tumors.  Most solid tumors are aneuploid, and p53 has been implicated as the guardian of the euploid genome.

How long did the pulse of cancer stay in human cancer data from the Cutter incident of the Polio vaccines?

Bernice Eddy found the SV40 in the Salk vaccine and told the world about it in th emid 1950s’  The NIH and FDA ruined her career over her admission and scrubbed their websites.  Most people ran from studying SV40 after this event in centralized science until the Nixon administration. What cancers in humans are linked to SV40 contamination?

In the 1970s, David Lane & Arnie Levine started studying a virus called SV40. Their interest was in a viral gene responsible for transformation, the SV40 oncogene called large T antigen.  Lane’s task was to extract the large T antigen protein from cells infected with SV40. He used electrophoresis to separate the protein molecules based on size and charge.  Whenever he ran electrophoresis to purify the large T antigen, he always found an unknown protein with a molecular weight of 53 kilodaltons. Initially, others in Lane’s lab thought it was a contaminant or a breakdown product of the large T antigen.  As reports of this protein came from other labs too, it was named p53 based on its molecular weight.

In 1979, immunological studies identified the p53 protein due to its immunoreactivity with tumor antisera, suggesting its role as a tumor-associated antigen. Everyone was convinced they had found a new oncogene. The excitement was high!  Wait a minute—did I say oncogene? p53 is actually a tumor suppressor gene! This is my favorite plot-twist of the p53 story: its mischaracterization as an oncogene.  The initial misclassification was due to the research climate of the time (1980s). Oncogenes were thought to be the key to understanding cancer, and the idea of a tumor suppressor gene was in its infancy.

As mentioned above, p53 was initially found bound to the major oncogenic protein of SV40, so it was understandable at the time to think it must be an oncogene as well. However, some experimental observations did not fit well with the idea that p53 was an oncogene.  In 1986, the first tumor suppressor gene, Retinoblastoma gene (RB1), was discovered, confirming Knudson’s Two-Hit hypothesis.  In 1989, this two-hit model was applied to p53, specifically in colorectal tumors. It fit this model, as in virtually all cases, both copies of p53 were mutated.

This conclusion was confirmed by subsequent findings that patients with inherited mutations of p53 were predisposed to diverse tumor types. Mice with engineered “knock-outs” of the p53 gene were also tumor-prone.  Today, more than 70,000 research papers are published on p53, making it the most studied human gene in history. Mutations in p53 are found in >50% of human cancers.  “It’s impossible or very difficult to get a malignant tumor without the activity of p53 being disrupted.” ~Bert Vogelstein, a legendary figure in p53 story who was the first to termed it as a tumor suppressor gene.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855935/

SUMMARY

New centralized data does not support a role for p53 in aneuploidy surveillance in organotypic cultures. There is strong evidence indicating that the loss of p53 is associated with chromosome instability and poor prognosis in the development of several cancers. See the papers (Donehower et al., 2019; Foijer et al., 2014; Fujiwara et al., 2005; Watson and Elledge, 2017)

When p53 goes awry the majority of tumors show varied TP53 mutations based on the following papers: (Clausen et al., 1998; Muller and Vousden, 2013). Live-cell imaging of Trp53+/+ and Trp53 & mCOs showed that mitotic errors, including lagging chromosomes and multipolar mitoses, occurred frequently in cells lacking p53, consistent with several published studies (Artegiani et al., 2020; Drost et al., 2015).

The bottom line issue for me? Decentralized science must show that when p53 signaling goes awry, it corresponds to a lack of ultraweak -UV biophoton production at the mtDNA level. This is why apoptosis goes awry and this also corresponds to the following variables: Low mtDNA melatonin production, low mtDNA water production, and altered mtDNA CO2 production in most solid tumors. This results in cell cycle arrest and cells begin to migrate to other tissues that have the ability to generate the ultra weak UV biophotons to complete the cell cycle.

 

CITES

1. https://www.pnas.org/doi/full/10.1073/pnas.1431692100

2. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208645/

3.  https://x.com/DrJackKruse/status/1804162237528998309

4. https://x.com/DrJackKruse/status/1803877114598314228

For light to have a biological effect, photons must be absorbed by photoreceptors in the living body or there is no effect. ROS/RNS creation in mitochondria and oxygen begin this process.

H202 is a type of ROS made in mitochondria when we are healthy. When do we make ROS during the day? Daylight is associated with higher electric fields and lower magnetic fields and this correlates to mornings having higher ROS production. The morning AM ROS burst links to the PER2 gene in the mammalian clock mechanism. These effects are rooted in the spin selected ROS partitioning between peroxide and H202, known as the radical pair mechanism

When you add hydrogen perioxide to tissue heat is released and this heat is a clue that light is being liberated from the atoms in matter in your cells. I do this in almost every surgery I do but rarely tell people why I am doing it or how it works. My surgical team sees a lot of bubbles released and those bubbles are hydrogen gas being liberated at the same time. But there is more magic below the cell level to help my patients get better. I got the idea from radish roots.

This study below investigates the spontaneous emission of biophotons from radish root cells and the effects of various treatments on this biophysics phenomenon.

Key findings in the paper:

1. Freshly isolated radish root cells exhibit spontaneous biophoton emission at a rate of about 4 counts per second. This is an ultraweak photon release.

2. Addition of hydrogen peroxide (H2O2) to the cells from matter in cells significantly enhances biophoton emission from cells up to a rate of about 500 counts per second. When I read this I said I know how I can improve redox in the surgical site of my patients. This light has a specific spectra in the case of radish roots. This varies in eukaryotes like mammals.

3. The enhancement of biophoton emission by the addition of H2O2 is completely abolished when molecular oxygen is removed by using a glucose/glucose oxidase system or when reactive oxygen species (ROS) are scavenged using reducing agents such as sodium ascorbate and cysteine. This is a big clue glucose is not the real problem in cancer, unfettered light release to alter the nuclear genes is by excessive ROS. This tells you why cancers always are associated with their own brisk blood supply to keep oxygen humming to create light cells are missing to get through mitosis. That light is ultraweak UV light.

4. Spectral analysis of the H2O2-induced biophoton emission shows that biophotons are mainly emitted in the green-red region of the spectrum in radish.

5. The energy for this biophoton luminescence in cells is produced when an excited biological molecule drops to a lower energy state and the majority of the excited biological molecules are reactive oxygen species (ROS) Singlet oxygen, systematically named dioxygen and dioxidene, is a gaseous inorganic chemical with the formula O=O, which is in a quantum state where all electrons are spin paired. It is kinetically unstable at ambient temperature, but the rate of decay is slow.

Singlet oxygen (represented as 1ΔgO2, abbreviated as 1O2) is not a radical and represents an excited state of O2 in which the spin of one of the unpaired electrons is changed to yield two electrons with opposite spins. The terms ‘singlet oxygen’ and ‘triplet oxygen’ derive from each form’s number of electron spins. The singlet has only one possible arrangement of electron spins with a total quantum spin of 0, while the triplet has three possible arrangements of electron spins with a total quantum spin of 1, corresponding to three degenerate states. An excellent way to detect the presence of singlet oxygen is using steady-state or time-resolved measurements of its characteristic phosphorescence at around 1270 nm. Phosphorescence is a process in which energy is absorbed by matter in a cell and is released relatively slowly back into the cell 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. In mammals the amount of light is absorbed quickly by chromophore proteins to be used for signaling. This is why surgeons do not see what is clearly there during surgery. Plus, humans retina cannot see NIR light at 1270 nm . So how do we know this light is present? We use machines that can detect it.

Electron paramagnetic resonance (EPR) spin-trapping data shows that the formation of singlet oxygen is observed after addition of H2O2 and correlates with the enhancement in biophoton emission.

These findings in the paper below provide direct evidence that singlet oxygen is involved in biophoton emission from radish root cells. The results suggest that the biophotons are generated through a process involving the formation of singlet oxygen, which emits 1270nm light in the NIR range of the spectrum whose production can be enhanced by the addition of hydrogen peroxide.

 

SUMMARY

We know about how radish roots do it, but what about us when the solar cycle is awry?

Melatonin as a potent antioxidant and anti-inflammatory agent is known for protection of normal tissues against ionizing irradiation. This tells us that is has to be a control switch for ROS creation. Bright light and heat lowers melatonin effects and dark and cold temperatures increase its effects. Melatonin clearly is linked to ROS creation in some novel way. What do we know about sunrise? Light dominates the environment and the electric ield in the plasma called the ionosphere increases. The magnetic field of the gases in that ionosphere increases. 21% of the atmosphere is made of oxygen that is paramagnetic and this causes it to be drawn to tissues with high mitochondrial capacity. lWhen the sun rises, ight (photons) begins transfers energy to matter, causing the electrons to be emitted. What is it about electrons that maybe the clue to this mystery?

If you look back to Becker’s work he warned us about about the negative effects of electropollution. He also taught us about magneto pollution to a lesser degree. He also showed us how strong gauss magnets were able to induce anesthesia in salamanders before surgical procedures. He told us about the effects he and Marino found along electric power lines in Upstate New York in human subjects.

MAMMALIAN IMPLICATIONS OF THIS?

The TCA cycle produces more reducing power with a 22 ATP gain from its reducing power while glycolysis only produces 6 ATP from reducing power and Pentose phosphate group varies in the number of reducing power it produces. This tells us glycolysis and the TCA cycle on a relative basis vary greatly in how much ATP and ROS they produce.

Metabolic rate, when viewed from ATP creation is driving a developmental timing mechanism in a cell. But something must act as an off and on switch.

We know from the video about that 1270nm light equalizes the amount of ATP and ROS they produce. This appears to be the tipping point between day and night to act as an off and on switch in some way.

The implications are vast for many diseases from cancer, healing, autoimmunity, and to mastocytosis. How so?

For close to 15 years I have been giving major clues out to my tribe that magnetic fields are linked to circadain clock biology. How do they link is the biggest mystery in decentralized science. This blog explains the link CLEARLY.

The centralized assumption that I have always rejected has always been that the eye mainly senses light, whose local distribution is transmitted to the brain in a kind of copy by a mosaic of impulses. This is an idea so obvious to abuse by Nature to encode a hidden message in how life really operates. Instead of accepting that assumption, I looked for evidence in the literature of researchers who were wiser and actually thought about attaching electrodes to the animals who made it through the last extinction effect optic nerves so we might be able to eavesdrop on the signals Nature was really sending to message. I found evidence in amphibians where researchers positioned an aluminum hemisphere around a frog’s eye and moved objects attached to small magnets along the inner surface of the sphere by moving a large magnet on its outer side. This effect was eerily similar to the effects found in Becker’s work on regeneration and salamanders. This simple experiment showed me that non visual photoreception was the mysterious behind what Nature was doing. Then I jumped hard and looked for more zebra’s. And I found them in the eye of mammals and wrote the evidence in slides for talks I gave all over the world.

WHAT IS THE ELECTROMAGENTIC INFORMATION CELLS LOSE WHEN OUR EYES GO AWRY?

Think about what I have said about the European Robin eyes and the cryptochrome gene for 20 years now. The answer is buried there.

The development of the radical pair mechanism used for magnetoreception in bird retina has allowed for explanation of the fact that magnetic fields are observed to have an effect on chemical reactions speed in animals that made it through the last extinction event. It turns out the same mechanism found in birds, and their ancestors, theropod dinosaurs is also found in all mammals. The eye speaks to the brain using Nature’s most hidden recipe built in a language already highly organized in atomic physics, clocked and expertly interpreted, instead of transmitting some more or less accurate copy of the distribution of light on the receptors.

This quantum mechanism describes how an external magnetic field can alter chemical yields by interacting with the spin state of a pair of radicals.

The radical pair mechanism is based on the dependence of product yields on

1) the hyperfine interaction involving electron spins and neighboring nuclear spins of atoms and

2) the intensity and orientation of the geomagnetic field.

3) the chemical reaction kinetics in radical pair mechanism (RPM) is related directly to the qualities contained in the magnetic field in question. Overall, the spin evolution between singlet and triplet states in ROS/RNS radicals are affected by the magnetic field, is the key feature for radical pair mechanism.

4) Early proponents & biophysicists missed the magnetochemical effect in cells and focused on light chromophores.

This told my decentralized mind that one needs to know the general scheme of chemical reactions involving radical pairs generated from singlet and triplet precursors; one needs to understand the spin dynamics of the radical pairs; and the magnetic field dependence of product yields caused by the radical pair mechanism. It also told me I needed to understand solar cycles and disease patterns better.  This told me I needed to look carefully at the eye of birds where the RPM mechanism was discovered in the mid 1970s. So that is what I did. If you go back and look at the Cold Thermogenesis #6 blog post you’ll see what I said there about the eye and spin dynamics. It was all there early.

During summer solstices did you know that pipes corrode faster than normal? Do you know why this happens? It is the same reason bipolar patients symptoms get worse during the summer solstice: Magnetic field strength is at its strongest. Did you know the Pandemic of 1918 also was linked to solar dynamics and magnetic strength? The majority of pandemic influenza outbreaks since 1700 CE were associated with minima and maxima of sun spot numbers linked to the 11 year solar cycle. In fact, seventy-four percent of influenza pandemics and epidemics (26/35 events) since 1700 occurred at or within one year of the peak or trough in sunspot numbers, increasing to 89 percent (31/35) within two years. This links magnetic field strength to immune function.

Chemical reactions in our immune system that involve radical intermediates are influenced greatly by magnetic fields. These fields act to alter their rate, yield, or product distribution. These effects have been studied extensively in liquids, solids, and constrained media such as micelles. None of these are well studied in centralized medicine. They will be well studied in El Salvador’s new decentralized system. It maybe the earliest detection system of disease we have today.

CONSIDER THIS EXAMPLE:

The involvement of singlet oxygen in biophoton emission has implications for our understanding of many diseases like mast cell disease in the skin that links to immune function. Mast cell dysfunction is linked to an absence of 1270 nm light in skin of mammals. Singlet oxygen is known to liberate this frequency of light as the picture below shows. People with mast cell disorders do not make enough hydrogen peroxide from their mitochondrial respiration. As a result, with a comorbid lack of sunlight containing 1270 nm light and lack of H202 creation in tissues is asosciated with immune dysfunction in mast cells. There is a lesson here that radishes are teaching us about mastocytosis.

People with cancer, autoimmunity, mastocytosis, and poor wound healing always are deficient in AM sunlight. Why? This is when we get a lot of NIR light that has 1270nm light. Early morning 6AM -9AM sunlight has a relative irradiance that has a higher amount of photons in the visible and NIR spectrum compared to midday exposure (noon). The picture tells why you decentralized medicine always recommends AM sunlight. This sun time = TINA = THERE IS NO ALTERNATIVE. You remember that recent blog?

All of you know about the COVID pandemic. Do you know that it began during a weak solar cycle. This was my first evidence that the 2020 Wuhan flu was manufactured because it made no sense based on what I know about immune cell function. What prediction can I make right now about those who took the experimental treatment? 2024-2026 will be deadly for those people. Why?

The 1918–1919 pandemic flu virus happened during during an exceptionally strong solar cycle and caused acute swelling of and bleeding from the lungs from the healtiest people on Earth, and people who were infected typically suffocated within one to two days. Most were men in great metabolic shape. The second wave of the pandemic was responsible for the most deaths, due to an unusually severe hemorrhagic pneumonia. Today, in 2024 we just had 4 massive CMEs where the aurora’s were seen into the tropics, and the people who were the most healthy are dying at unbelievable rates now as evidence by my Tweets over the last 9 months. How did i know in 2020 this was coming. I know history and I know about the RPM mode of transmission to ROS/RNS.

H5N1 is bird flu. Why is the CDC, FDA, and WHO warning today’s COVID jab victims today about bird flu? Because they know they caused the COVID pandemic accidentally via gain of function study in Wuhan and now they are seeing evidence of patients in the experimental group who are beginning to experience similar pathologies to those of the 1918–1919 pandemic. Namely they are EXPECTING MASSIVE acute respiratory distress syndrome to overwhelm high vaccinated populations. This is the collateral effect they fear. The act of blocking your eye or skin from the sun around these coming dates might be a deadily choice for many. Also on these dates I expect we will have serious political and economic news hit to change sentiment rather quickly. Neurologic processing changes this way when ROS/RNS peaks.

HOW DO YOU TREAT IT BEST?

ARTIFICIAL RED PANELS DO NOT EQUAL AM SUNLIGHT EVER.

The radical-pair mechanism explains how a magnetic field can affect reaction kinetics by affecting electron spin dynamics. Most commonly demonstrated in reactions of organic compounds in cells involving their radical intermediates, and a strong magnetic field can speed up a reaction rates by decreasing the frequency of reverse reactions. This is why bipolar patients are acting very bizarre this year. It is also why those with neurodegeneration are having wild swings in their symptoms day to day now. Look at the narratives around Biden’s behavior lately. It is all controlled by the puse of ROS his defective mitochondria are making during this tumultuous time as we revovled around the sun.

Mitochondria act as signaling organelles in low-oxygen conditions. Hypoxia (0.5–3% oxygen) increases mitochondrial ROS that activate transcription of adaptive genes. Anoxia (0–0.5% oxygen) initiates mitochondrial outer membrane permeabilization (MOMP) to activate cell death. You’ve been given an amazing piece of decentralized science today. Use it wisely.

My predictions for my tribe in SOLAR CYCLE 25?

Know your solar history and you choices around the jab. On September 15, 2020, the solar minimum occured between Solar Cycle 24 and 25 – the period when the sun is least active – happened in December 2019 when Wuhan virus escaped. When I reviewed the 13-month period, the smoothed sunspot number fell to 1.8. The only part of the government who told the truth at this time was NOAA and NASA. According to the Solar Cycle 25 Prediction Panel they are praying for weak Solar Cycle 25 because of the lab leak. Early 2024 results however, have showed their guesses were WRONG. They expected peak sunspot activity expected in July of 2025, but within the last month we have had spectacular CME from sunspot activity that hit Earth. This is why so many people with jab injuries, mental illness, clots and cancer are hitting my emergency room like nuts the past 6 months. I expect the July 2024 – July 2025 Solar cycle to be DEADLY.

The Solar wind energy striking the Earth’s magnetosphere affects the entire environment because the pressure on the region increases and the magnetosphere shrinks sometimes four Earth’s radii. This sudden compression causes earthquakes in specific plates. We’ve had a quite a few more earthquakes in El Salvador the first 6 months of 2024. Maximum quake frequency occurs at times of moderately high and fluctuating solar activity. Terrestrial solar flare effects which are the actual coupling mechanisms which trigger quakes appear to be either abrupt accelerations in the earth’s angular velocity or surges of telluric currents in the earth’s crust. It appears even earthquakes are magnetochemical.

Solar Cycle 24 was average in length, at 11 years, and had the 4th-smallest intensity since regular record keeping began with Solar Cycle 1 in 1755. It was also the weakest cycle in 100 years. Solar maximum occurred in April 2014 with sunspots peaking at 114 for the solar cycle, well below average, which is 179.

Solar Cycle 24’s progression was also unusual and why NO PANDEMIC should have hit us at this time. This is why I knew in 2020 that this was a gain of function Lab leak manufactured problem. Now you know why I was so on top of it. in 2024 the Sun’s Northern Hemisphere led the sunspot cycle, peaking over two years ahead of the Southern Hemisphere sunspot peak. This resulted in solar maximum having fewer sunspots than if the two hemispheres were in phase. This has a lot to do with the changing of the magnetic poles in the Northern hemisphere now. The magnetic North Pole is now in the UK. Recall, last summer I visited this area. Now you know why.

Solar Cycle 25 PREDICTIONS for the EXPERIMENTAL GROUP AND THOSE WITH LOW REDOX
For the last eight months of 2023, activity on the sun steadily increased, indicating we transitioned much more rapidly to Solar Cycle 25 in the first 6 months of 2024. More people already sick with diseases will die sooner. Kids with autism will struggle more this year. People who have a framshifted genome will get sicker quicker and die more rapidly than their centralized MDs expect. The more healthy they are, the more likely they will get sick and die. It is only shocking when you DO NOT UNDERSTAND THE BIOPHYSICAL LESSONS IN THIS BLOG.

I have a sense Solar cycle 25 is also going to be be unusual with more strength and higher peak of sunspots than NASA and NOAA expects. In Solar cycle 25 NASA said they expected only 115 sunspots. The first 6 months of 2024 told me otherwise. We are experiencing it right now based on the recent auroras and the weather in the tropics. We are seeing this in the radical changes in President Biden’s behavior and his mental state. Right now El Salvador is getting smoked by harsh weather NOAA/NASA/Bukele did not expected. This is why I am making my predictions to you right now. Right now people are getting more sick and dying who should not. I know why. This blog has those answers. ROS is out of control in living things.  Few see what I see.

What was buried in the CT #6 blog? How quickly solar activity rises is an indicator on how strong the solar cycle will be and how diseases states will react. Share this uncommon adivce with your loved ones.

CITES

https://pubmed.ncbi.nlm.nih.gov/20106674/

Rodgers, C. T. Magnetic field effects in chemical systems. Pure Appl. Chem. 2009, 81 (1), 19–43

https://www.patreon.com/posts/19082581

 

There has been some recent news out about folate levels, sunlight and artificial light. Many people do not know folate is a photosynthetic chemical and it links dark skin (melanin) for natural folate protection.

We have clear evidence (Cite 1) that ultraviolet radiation affects directly in proportion to folate human blood. Seasonal cycles repeat annually and light stability is more common at low latitudes. Therefore, the amount of photosynthetic chemicals we use acts as a photosensitizer to our chromophore proteins. This has big implications inside the tropics. The percentage of low folate values increases in summer by almost 3.5 percent in comparison to winter. Moreover, geneder differences are huge. Overall folate levels are lower in men as compared to women, regardless of seasonality. This makes sense because of who has the children.

Vitamin B9 (Folate) was first extracted from spinach leaves in 1941. The term folate comes from the same root as foliage: green and leafy. Folates are vital: they accept carbon atoms and pass them on as needed as the fundamental basis for proper methylation. This implies that during summer months folate levels should be expected to be at their lowest levels NATURALLY.
Folate biology has a specific and tight seasonal control mechanism linked to light.  This is not a food story at all 

What if there is no seasonal or light controls in place? 

Folate is often given to pregnant women to prevent spinal dysraphisms today. This is something pediatric neurosurgeons deal with and why I know a lot about them.  The incidence of these conditions has dropped but it is has done at a COST.  Why?  but too much folate/folic acid causes cognitive haze and sleep difficulty and may cause neural migration problems in artificially lit environments.  This should awaken you what I wrote in Quantum Engineering #45..   In North America, (CAN/USA) folic acid was added to all grains in 1996.  This is only a few decades ago and we are seeing the transgenerational effects of this right now in our children’s disease phenotypes.

In general, it does not appear that even large amounts of folic acid taken orally are acutely toxic in adults. However, given the fundamental role of folate levels in synthesizing nucleotides (including RNA and DNA) and in methylation reactions as a methyl donor, high levels may have inadvertent implications for proper methylation of DNA during times of rapid cell division, such as in prenatal development. You’d think the idea that adding folic acid to the food supply might have caused centralized medicine to expect unintended consequences.  Few thought about, much less studied it.  I have always been worried about this effect since I learned that B12 was a photoreceptor in humans.  (slide from Vermont)

This idea has been speculated in research circles as early as 2005, and specifically speculated to be relevant for the increase in autism in 2011.
MOST PEOPLE WITH MTHFR DEFECTS ARE SUPERSENSITIVE TO LIGHT VARIATIONS

An early review of potential problems with mass folic acid supplementation of the food supply was undertaken by Lucock and Yates. Here, they noted that a drastic increase in folates could lead to a selection for the previously rare MTHFR genetic substitution of T for C at area 677 (MTHFR C677T), and that if folic acid is supplemented at doses above 400 mcg that unmetabolized folic acid will circulate in the blood supply at a level largely consistent with the excess dose. In 2005, Lucock and Yates noted that high levels of folic acid in the blood does not generally occur as a result of ingesting natural folates and that “no work has been done so far to evaluate the biological and genetic consequences of excess long term exposure” to these circulating folic acids on DNA/RNA biology. After that review, there were two separate findings of unexpected increases in asthma and breathing problems associated with folic acid use.
It now appears that we have clear data that excessive methyl donor transfer has significant epigenetic effects in humans. This work dovetailed with another review questioning the wisdom of mass folic acid supplementation published in 1996. Smith et al. pointed out that by supplementing the food supply; several hundred thousands of persons are exposed to greatly increased levels of folic acid. These authors noted that prior research had shown that expectant mothers with low vitamin B-12 (most vegans/vegetarians) AND high levels of folic acid were associated with offspring having an unexpected increased risk for insulin resistance and disease associated with this condition.  This is worrisome when you know that blue light exposure does the same thing and more.

Troen et al. found that some women past childbearing age subjected to high folic acid supplementation may be at risk for reduced immune system functioning causing inflammatory autoimmune conditions to spike. This problem has gotten worse since I first looked into it in 2005.

Did you know mammals exhibit genomic instability under conditions of folate deficiency in the skin. Remmber your skin is a neuroectodermal derivative. A lack of folate adversely effects your skin’s cellular capacity to handle UVR light. This is why so make pale gingers burn so fast. Moreover, did you know that optimizing folate levels in skin is beneficial in preventing or repairing the pro-carcinogenic effects of UVR exposure? Folate restriction by any modern excuse leads to rapid depletion of intracellular reduced folates resulting in S-phase growth arrest. Did you know this leads to ncreased levels of inherent DNA damage, and it causes increased uracil misincorporation into DNA. This is called a frame shift mutation and it is how light can cause transepigenetic signaling. This frameshift mutation will not cause a significant loss in overall cellular viability. It is how mammals adapt to changing seasonal light environments. Folate depleted keratinocytes can be sensitized toward UVR induced apoptosis. This changes the biophoton spectra emission from mtDNA and this displays a diminished capacity to remove DNA breaks. This allows for changes in phenotype. This occurs by photo and oxidative DNA alterations. Your dermatologist likes to call this damage, but Mother Nature uses this for seasonal adaptation in your skin. When this occurs more UVR = more melanin production. This protects your folate stores from degrading. Nature is amazing when you see her recipes. Dermatolgyis dangerous because they do not understand what she is doing on your behalf. Thus, folate deficiency creates a “permissive environment for genomic instability to allow for seasonal change. It is not an early event in the process of skin carcinogenesis or autism. If one abuses the use of folic acid and blue light than you can and will get diseases. The effects of folate restriction, even in severely depleted, growth-arrested keratinocytes, were reversible by repletion with folate foods. In summertime, foods with folate are plentiful in the tropics for this reason. Photosynethesis always has our cells backs.

 

FOLIC ACID SUPPLEMENTS EXACERBATE MTHFR DEFECTS

Methylenetetrahydrofolate reductase (MTHFR) is an enzyme encoded by the MTHFR gene and has significant implications in the field of decentralized medicine. This enzyme plays a critical role in the folate metabolism pathway, which is integral for processes like DNA synthesis and repair, as well as epigenetic alterations via methylation by light variation. Variants of the MTHFR gene are associated with altered enzyme activity, which can, in turn, affect mtDNA heteroplasmy and disease phenotypes. This happens by alterations created in the spectra of biophotons made via metabolism. You’ll hear more about that soon enough.

Increased consumption of folic acid is prevalent in our modern world, and has negative consequences for MTHFR patients.. The effects of folic acid on the liver, the primary organ for folate metabolism, are now being unfolded. Methylenetetrahydrofolate reductase (MTHFR) provides methyl donors for S-adenosylmethionine (SAM) synthesis and methylation reactions.

New data now suggests that high folic acid consumption reduces MTHFR protein and activity levels, creating a pseudo-MTHFR deficiency in the liver and skin of mammals. This deficiency results in hepatocyte and keritinocyte degeneration in both organs, suggesting a 2-hit mechanism whereby mutant hepatocytes cannot accommodate the lipid disturbances (how fatty acid carbon lenghts are dealt with and how melanin operates in the skin) and altered membrane integrity arising from changes in phospholipid/lipid metabolism. People forget the skin biology needs optimal light to control the lipid rafts in the skin as seasons change. Folic acid destroys this ability. This data has clinical implications for individuals consuming high-dose folic acid supplements, particularly those who are MTHFR deficient.

WHAT ABOUT CYP VARIANTS?

CYP enzymes are heme based and subject to blue light toxicity. They have been identified in all kingdoms of life: animals, plants, fungi, protists, bacteria, archaea, and even in viruses. This is why so many astronauts have viral particles in the blood and space is known to foster cataracts and protein folding issues in the eye. However, they are not omnipresent in all bacteria; So space blood infections vary compared to the ones we see on Earth. More than 50,000 distinct CYP proteins are known to man.

Most CYPs require a protein partner to deliver one or more electrons to reduce the iron (and eventually molecular oxygen). Remember electrons must be excited by sunlight to use the photoelectric effect in the photon traps in aromatic amino acids. Based on the nature of the electron transfer proteins, CYPs can be classified into several groups: I covered this with Rohan during a past Sunday Q & A that lasted 5 hours. Members should listen back to those recorded Q & As to refresh their minds.

• Microsomal P450 systems, in which electrons are transferred from NADPH via cytochrome P450 reductase (variously CPR, POR, or CYPOR). Cytochrome b5 (cyb5) can also contribute to reducing power to this system after being reduced by cytochrome b5 reductase (CYB5R).
• Mitochondrial P450 systems, employ adrenodoxin reductase and adrenodoxin to transfer electrons from NADPH to P450.
• Bacterial P450 systems, employ a ferredoxin reductase and a ferredoxin to transfer electrons to P450.
• CYB5R/cyb5/P450 systems, in which both electrons required by the CYP come from cytochrome b5.
• FMN/Fd/P450 systems, originally found in Rhodococcus species, in which an FMN-domain-containing reductase is fused to the CYP. (cytochrome 2 in humans is related to this system.
• P450-only systems, which do not require external reducing power. Notable ones include thromboxane synthase (CYP5) for platelets, prostacyclin synthase (CYP8) for PG synthesis, and CYP74A (allene oxide synthase). You should begin to see just how we are beings of light who need solar programming by sunlight and not man-made light.

Anything transferring electrons to proteins = a semiconductive circuit. When you understand the photoelectric effect only works with photons and electrons you begin to see why SNP status are mostly superfluous and generally do not matter when you’re in the sun chronically and you have melanin in your integument and interior properly renovated.

Melanin operates in us to charge separate water into its components of H+ and oxygen and 2 -4 electrons. The level of oxygen dissolved in cells is critical in varying the ultraweak biophoton signature from metaboilsm. Those two electrons liberated from charge separation obviate the need for exogenous and endogenous sources of electrons (grounding/food). SNPs evolved because mammals varying in how they ground and what they eat based on latitude and what photosynethesis can provide. SNPs and SAPs tell vary in how melanin biology is operating. They are like equalzer buttons for music made in cells.

People with a lack of melanin think SNPs matter way more than they do because functional medicine MDs tell them this. This is incorrect. Pale people without enough melanin lack electrons to run their semiconductive circuits. You’d be wise to avoid that level of centralized thinking in the future. Folic acid lowers electrons = lowers your redox power.

How humans operate is specific to humans and not to other mammals. Most of the BH4 and Vitamin C used as cofactors deliver electrons to the biochemicals. BH4 and Vitamin C deliver the exogenous sources. Melanin delivers the endogenous source of electrons. Humans create massive amounts of electrons when POMC is operational in their tissues. Here you see Noether’s thereom show up yet again.

THE SUN IS THE BEST SOLUTION TO THIS PROBLEM

SUNLIGHT reduces all these risks, while modern lighting exacerbates it.  Moreover, it appears nature is trying to tell us that the sun raises melanin and melanin is protective.  Strong solar cycles in photosynthesis seem to simultaneously lower folate in foods in the summertime for a deep reason. That reason is epigenetic hypermethylation which can lead to sleep apnea and cancer formations later in life due to altered DNA methyl marking. This process also alters how RBC circadian cycles (ferrodoxin) can work within their circadian cycles with the innate immune system and TOLL receptors.  Most people with anemias have this intrinsic problem linked to modern behaviors around light.

Folate is destroyed by strong sunlight with both UVA and UVC light. Darkened skin protects the stores we have, but there is now proof that folate levels are designed to be low when the solar radiation is strong in the local environment. These days most people are eating food humans have been engineered and/or genetically altered in some way. Then add in the effect of Artifiical light day and night.  This throws off the normal variation of the natural folate cycle during seasons. Today, people in developed countries are getting MASSIVE amounts of folates in the form of folic acid. This is the real reason to avoid grains.  Folates are now being ingested in three ways: as natural folates from food, as synthetic folic acid added to processed grains and synthetic from vitamin supplements.  All of these idea are counter evolutionary to Nature’s laws.

SUMMARY

Methylation patterns are linked to how light is transformed in a cell. When sunlight is absent for any reason mitochondrial redox drops. When this happens energy transformation drops. As a result of a lack of energy methylation problems shows up in both genomes. Decentralized clinicians know what to look for. Allopathic and function docs would know what to look for because they still have no idea that light controls the enzymatic flux in metabolic pathways.

Loss of mitochondrial redox power causes methylation problems to manifest in your labs without any SAP/SNP issues present in your MTHFR survey or nuclear genome. Very few clinicians know a lack of sunlight causes methylation defects.
It shows up in your labs in a very specific pattern of results as an accumulation of methionine and S-adenosylhomocysteine, with low or low-normal levels of S-adenosylmethionine (SAM) and homocysteine. PBM treatment fixes it. Sunlight is always the best treatment. Supplements not so good.

As a result of the supplementation of folic acid, the circulating level of unmetabolized folic acid, as well as total folates, has greatly increased over the past generation, probably to levels largely unprecedented in human history.

Folic acid has been shown to be able to epigenetically alter the functioning of the genome and to have long term effects on gene expression as I mentioned above.

The Centers for Disease Control Vaccine Safety Datalink data set compared children with autism to control children on several variables. Many people who think the link of vaccines to autism might be shocked to find out that folic acid supplementation during gestation is associated with a serious increased risk for autism. I believe the combination of artificial light and folic acid supplementation are causing neural migration problems.  This is why parental melanin levels are important clues.  This effect remains even when health-seeking behaviors and other variables are controlled. This is information parents of kids with AUTISM need to know. Autism, asthma, allergy, ectopy, eczema, diabetes T1D, T2D, and MODY, auto-immunity, and spinal abnormalities have their lowest incidence is lowest in equatorial environments and it appears now we know why this is the case.  This is decentralized medicine 101 I will bring to El Salvador.

CITES

 

1. Valencia-Vera E, Aguilera J, Cobos A, Bernabó JL, Pérez-Valero V, Herrera-Ceballos E.. ‘Association between seasonal serum folate levels and ultraviolet radiation’. ‘J Photochem Photobiol B’. 2019 Jan;190:66-71

2. https://threadreaderapp.com/thread/1656714608793485326?refresh=1683832764

3. https://www.linkedin.com/article/edit/6330012027309875200/

4. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862485/

5. https://en.rattibha.com/thread/1798513232203673687

The circadian system orchestrates the temporal organization of many aspects of physiology, including metabolism, in synchrony with the 24 hr rotation of the Earth. Like the metabolic system, the circadian system is a complex feedback network that involves interactions between the central nervous system and peripheral tissues. Massive amounts of emerging evidence suggests that circadian regulation is critically linked to metabolic homeostasis and that dysregulation of circadian rhythms can contribute to all diseases. Conversely, metabolic signals feed back into the circadian system, modulate by applying what circadian gene expression is based on the light sensing from the environment. This alters behavior and disease phenotype. A loss of circadian periodicity causes metabolic derangement. Light controls food at all levels.

The podcast above was all about the treatment of idiopathic intracranial hypertension that manifests with optic nerve swelling, visual changes due to retinal blood vessel defects, and headache.  You might be surprised to know that idiopathic intracranial hypertension (IIH) is also associated with tinnitus.  That should stop you dead in your tracks if you are black swan mitochondria considering my recent podcasts and blogs here.  You now know that your cochlea is lined with melanin.  In fact, every sense organ is between the environment and the brain.

CPC stands for a clinico-pathologic conference that we often see in medical schools that are used for teaching students and doctors.

Today you are going to medical school, albeit, a decentralized medical school lesson how why light trumps food.

What did the centralized podcast lesson above miss?  Melanopsin has been found as the dominant opsin in the human brain but it is also found in blood vessels of the brain and is critical in relaxing these blood vessels.  What happens when there is melanopsin damage to the vessels of the retina and brain when there is associated melanopsin damage?  Do blood vessels relax or do they become stenotic?  Might this be what the group of endovascular neurosurgeons missed above?

I think so.

What happens when melanopsin damage occurs?  The weak covalent bond between it and vitamin is broken and Vitamin A is liberated.  The freed vitamin A destroys all the photoreceptors like heme proteins, nitric oxide, B12, monoamine oxidase, glutathione, and many others.  It ruins the ability of cells to use light to signal to and fro. Fidelity of signaling is destroyed.

Vitamin A is the first discovered fat-soluble vitamin and is primarily found in animal products or converted from dietary carotenoids in plant products. It is not a single compound but a group of derivatives including retinol, retinal, retinoic acid (RA), and some carotenoids according to different terminal functional groups.  In general, vitamin A refers to retinol, while retinoid refers to a general term that includes vitamin A metabolites and compounds and exhibits vitamin A-like biological activity.

Preformed vitamin A (usually from animal products) and provitamin A (including beta-carotene, usually from plant-derived food) are the two forms of vitamin A in the human diet. After being absorbed in the intestines, these two forms of vitamin A are converted to retinol and then oxidized to form retinal and RA to support the biological functions of vitamin A. The retinyl ester is the storage form of vitamin A in the liver and must be converted to retinol before being utilized, and these vitamin A derivatives are finally metabolized by the CYP26 family enzyme.

CYP26 enzymes = the cytochrome P450 family 26 enzymes in ALL chordates. This includes all mammals.

The metabolic barrier provided by CYP26 enzymes in various tissues such as the testes likely ensures that RA gradients are regulated by enzyme expression and activity within the tissue and not by circulating concentrations. Therefore, understanding the destruction, activity, and expression of CYP26 enzymes in individual tissues and cell types is critically important for defining the relationship between all trans RA concentrations and biological outcomes within a tissue. This means retinoic acids also control all sexual behavior and fertility as well. Today we have record rates of infertility and transgenerderism. The link both are linked to the light humans live under. Few see this links.

Previous studies have shown that retinoic acid (RA), the bioactive form of vitamin A, is involved in the regulation of various intracellular responses related to biological rhythms. RA is reported to affect the circadian rhythm by binding to RA receptors, such as receptors in the circadian feedback loops in the mammalian suprachiasmatic nucleus.

Many people wrongly believe solar light cycles are tied to Vitamin D and its receptor in the skin, eye, and brain. Few know about vitamin A and how it controls the human photoperiod in our brains where our POMC neurons exist. It is the major player in determining photoperiodicity in the human brain because of how Vitamin A is covalently bonded WEAKLY to melanopsin. When blue light dominates an environment humans lost their photoperiodicity and develop sleep problems.

Photoperiodicity is accounted for by biophysical changes in Vitamin A in the brain. It accurately mirrors the changes in the brain and the body that occur between the seasons when you are a careful observer.

At the equator, light doesn’t vary at any time of the year. As latitude rises light variation increases. Your body responds to every degree of latitude change via Vitamin A biology and POMC translation. Read that again.

When comparing the effects of the short days that occur in winter with the long days that occur in the summer Vitamin A (retinoic acid) swings in massive amounts. Researchers are finally beginning to understand how the brain converts the electromagnetic signal of light, first to an electric message (DC current), and then to a chemical one in the neuron synapse called a neurotransmitter. Vitamin A entangles the brain to the skin with its cousin Vitamin D. It is also critical in ephaptic communication I mentioned it to Dr. Huberman on Twitter and he brought it up during the Rubin podcast. Ephaptic signaling refers to extracellular signals generated by either a single neuron or a population of neurons, and the neurons need not be in physical contact. This likely has a quantum mechanical basis linked to coherence.

SUMMARY

Hypothalamic tanycytes are chemosensitive glial cells that contact the cerebrospinal fluid in the third ventricle and send processes into the hypothalamic parenchyma. Hypothalamic tanycytes sense vitamin A levels in the CSF. Did you know this?

We know that there are big changes between seasonal conditions on the planet even at the equator, and that seems to be how the wild animal controls weight gain and energy balance naturally in the environment. It also explains why obese women with IIH have massive alterations of Vitamin A too. Modern humans tend to gain weight in winter, and this is likely a new phenomenon related to their light environments. This is when they should be losing weight according to Nature’s laws. If you open any newspaper in January in the northern hemisphere, you will see tons of ads for New Year’s resolutions and gym memberships at this time to humans lose weight. This is unusual when you consider that wild animals do the opposite in January. Wild animals tend to get fatter going into the summer, and leaner into the winter when the light cycle is lowest and food is more sparse.

We now know that the human brain can sense retinoids, and regulate whole-body retinoid balance. This is how seasonal; light changes and local light changes sculpt the human ectoderm.

The reason becomes quite obvious when you consider that wild animals live by the dictums of their environment, but modern humans create their own environment via culture and socialization. This creation of their own environments destroys their photoperiodicity and dramatically alters Vitamin A signaling in the brain. Vitamin A is crucial in properly regulating the clocks tied to the hypothalamus that controls appetite, feeding, and energy balance. This is how quantum time is altered.

Today researchers have found that between winter and summer, retinoic acid changes dramatically in all mammals. There is a lot more to this ‘quantum dance’ of Vitamin A too. It appears there is much more powerful retinoic acid signaling during the periods of summer compared to the short days of winter. This implies that Vitamin A levels in the brain must be correctly tied to the seasonal alterations in ‘adiposity’ and depression result. Vitamin D gets all the press in the media, but Vitamin A control in your brain is way more important seasonally because of how it links to the POMC biology of melanin inside your body. It seems counterintuitive until you understand how QED works in the brain.

CITES

1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432198/

2. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283048/

3. https://advances.nutrition.org/article/S2161-8313(22)00023-0/fulltext

4. https://onlinelibrary.wiley.com/doi/10.1111/jne.12886

 

https://twitter.com/DrJackKruse/status/1701982061865632202

Larger size = more entropy in the PLL and disc = loss of circadian timing which leads to less energy transformation in the tissue degenerating.

The same thing happens in heart failure. The heart gets larger.

The same thing happens in stars. Star gets larger when they die.

The same thing happens in an ankle sprain. Ankles sprains lead to swelling.

What is the embryological origin of the spinal nerve like the one pictured above?

The ectoderm is also sub-specialized to form the neural ectoderm, which gives rise to the neural tube and neural crest, which subsequently give rise to the brain, spinal cord, and peripheral nerves. It also gives rise to neural crest cells that create melanin in the spinal nerve.

The melanocyte lineage is derived from the neural crest, which has its origins in the neural tube. Following its formation, neural crest cells delaminate from the dorsal-most aspect of the neural tube by a process of epithelial-to-mesenchymal transition. The neural crest delaminates from the developing neural tube and overlying ectoderm early in development. The pigment cells are the only derivative to migrate along the dorso-lateral pathway. This should tell spine surgeons that most diseases of spinal nerves that are associated with sensory findings are telling us precisely where our patients have lost melanin endogenously. This is why I make my cervical and thoracic disc patients remove their shirts to examine their skin. I am looking for signs of melanin destruction, lack of electrical conductivity, and count the number of nevus present in the skin of the affect nerve roots. I am also looking for evidence of melatonin and melanopsin disruption in the same dermatome. I also look for abnormal cholesterol deposits.

Mitochondria are dissipative structures in cells, but not the only ones. They transform energy and create order from the disorder in light energy they use to operate. The water mitochondria create is probably the single most important dissipative structure that life is based upon in cells. So I always look for signs of dehydration in the skin in the dermatome in question. I look at capillary refill and skin turgor.

I also shine a red light on the skin to see the response of the underlying blood vessels. you can see the red light above penetrates deeply into the dermatome.

After that test is done, then I cover the area for a brief time and shine a UV light on the same patch of skin and see how it effects the underlying blood vessels on the surface. If the become very visible, this tells me a a great deal about the NO reserve in this dermatome. There usually is a big difference in the etiology of disc herniations in this test. In acute injury the disc disruption is from biomechanical failure and no from photochemical degradation related to melanin loss. This tells me the status of NO production at this dermatomal level along with the melanin issues present in this nerve distribution.

Veins appear blue/green because these colors have shorter wavelengths that scatter more than red light. This scattering of shorter wavelengths is the same reason the sky is blue or eyes are blue. Your body does not produce blue pigment. Instead, near infrared light enters deep into your skin, hits your blood vessels, and is scattered back to you with blue being most visible and red largely being absorbed. So the color you see is blue, not red. You’ll notice this does not happen when blood vessels are closer to the surface (e.g. veins in your eyes, or skin when you blush)

Doctors and nurses use NIR light to find veins in patients. VIDEO

In difficult cases I will put a tourniquet in the limb in question and make blood pool and then do a prick of the dermatome to check for the HbA1C in that distribution. I call this my melanopsin and melatonin effect. Blue light and nnEMF exposures in dermatomes chronically induce melatonin suppression and this disrupts the circadian-regulated mechanism in the limb. This circadian damage leads to hyperglycemia and hyperinsulinemia in the body part that causes premature aging and higher heteroplasmy. These limbs often have many dangerous looking skin lesion in this.

The C4-5 disc herniation pictured above tell us a story about melanin in the C4-5 neural distribution. There was a lack of melanin in the skin of this dermatome. C4 provides sensation for parts of your neck, shoulders and upper arms. This dermatome is usually covered in humans who wear shirts. Cervical nerve 5 controls the deltoid muscles of your shoulders and your biceps. C5 provides sensation to the upper part of your upper arm down to your elbow.

In the developing embryo, dermatomes arise from somitic mesoderm, which develops from the middle layer of embryonic tissue lateral to the developing neural tube. Dermatomes are arranged with basic segmental pattern in the vertebrate trunk, although some overlap exists with similar areas above and below.

SUMMARY

This Tweeter thought he was being wise ass when he responded in the thread by saying this:

https://x.com/AttacheCrypto/status/1702121454127485171

You cannot tell whether a man is clever by his answers, but you do get a great sense whether a man is wise by his questions.

The business of decentralized medicine is to teach patients to live with some uncertainty. It is not to reassure them, but to upset them.  It sounds counterintuitive until you understand the perspective.  This perspective is built when you watch a great white shark attack.  As the shark digs its teeth into the carcass of a dead whale his teeth are replaced and his bite gets sharper.  This allows the shark to get to the liver and heart of the dead animal which in turn provides massive benefits to the shark. When you dig your teeth into your own assumptions, your teeth, too become sharper. Your mind allows you to dig deeper into a subject. You become what the world needs simply by helping yourself.  Questions open a space in your mind that allow better answers to germinate and connect with other ideas like turning a field over.

 

The status quo is the opiate of the mind.  The status quo is driven by seeking comfort, convenience, and the desire for stability, and a steadfast refusal to embrace the suck that life brings to us.  It is brought us by design.  We need to learn from our failures.  Seeking stability leads to complacency and stagnation.  You become a fool when you stop asking questions.  Always question before you comply with anyone or anything.

 

For centralized thinkers, the status quo is a powerful force that stifles innovation, creativity, and critical thinking.  The master key of wisdom is a persistent and frequent questioning of the status quo.  Our mind opens and awaken by embracing stress because it turns on the light inside of us when everything outside feels dimmed.  Become facile asking question where the answer makes a difference to society.

 

As physicians, it is our job to question the rules in existence and those being enforced on our patients; we are the ones that must ask if they are relevant or outdated, necessary or arbitrary, helpful or oppressive to the truth.  Without excellent questions no human progress is possible.

 

Thank you Crytpoattache for being a douchebag. You stimulated me to create a lesson for my tribe. Always embrace the suck folks. You’ll never know where it will lead you.

 

CITES

1. https://threadreaderapp.com/thread/1636019966947348480.html

2. https://x.com/DrJackKruse/status/1793770875646570938

3. https://x.com/DrJackKruse/status/1613303897791295488

What if I was to tell you the two most important biomolecules that do this is dopamine and melatonin, would you believe it? Dopamine derives itself from the breakdown of melanin. Melanin can be made accretively from dopamine as well. This allows life to experience the world as it is not. It provides cells a new lens, a new perspective of what life might be like when additional energy is added to the mix. Ironically, a loss of oxygen is how melanin becomes dopamine. When you turn your attention away from reality, dopamine jumps to action. It allows you to “move beyond the concrete”, to a realm that doesn’t yet exist. It motivates you to pursue, to control, and to possess a universe beyond your immediate grasp.

To make large collections of semiconductive proteins like dopamine and melatonin quantum coherent you need to link them together electrically.  Melanin does this for mammals.  Melanin in your skin and neuroectoderm conduct DC electricity.  This is what links these biomolecules.

Melanin is the master semiconductive protein in mammals. Dopamine can be the child of melanin degradation. But melanin can be made accretively from dopamine as well. It is a bidirectional pathway in mammals. Dopamine can be made many ways by mammals. This neurotransmitter is often referred to as the “reward molecule”. From my vantage point, life in the primate clade is based around the thrill of the chase, the anticipation of something new, and the excitement of getting something that’s novel and unexpected. It is what really gets our molecules buzzing.

IS MITOCHONDRIA: METABOLISM LINKED TO MELANIN RENOVATION ENDOGENOUSLY?

Dopamine and melatonin have to be linked electrically to become coherent. This tells us that there should be a deep tie in mitchondrial metabolism and the electrical coupling of dopamine and melatonin. What is it?

Amano et al. (cite 4) have provided a theoretical framework that demonstrates that resting tremor and other motor behaviors seen in Parkinson’s Disease are actually metabolically energy efficient. They posit that the role of dopamine, which can be a precursor to the formation of neuromelanin, and energy metabolism in the brain is linked and supported this assertion with research finding that “dopamine lesions result in reduced glucose uptake,” showing a preservation of energy, and dopamine is related to glucose metabolism. They conclude, “the loss of dopamine neurons in Parkinson’s Disease is likely to contribute to dysfunctional glucose metabolism.” Ironically none of them have made the link to why red light lowers blood glucose by 27% nor why when melanin is missing in cells endogenously, cells lose their ROS generation power from mitochondrial metabolism.

It appears that ROS and a lack of redlight production in mitochondria maybe the key link in diseases associated with altered glucose metabolism. They also note the growing amount of literature arguing mitochondrial dysfunction is common in Parkinson’s Disease and is causing metabolic dysfunction. They went on to say that they have discovered that there is an inverse relationship between melanin levels and mitochondrial ATP production. In fact, it appeared to them that melanin may hold the primary supply of energy while mitochondria produce supplemental energy, in an opposing, but complimentary, interdependent relationship.

BACK TO SUPERPOSITION OF DOPAMINE. MELATONIN, AND MELANIN

In quantum science, objects such as electrons and photons have wavelike properties that can combine and become what is called superposed. Particles are not the only thing that can be superposed. So can whole atoms. Did you know that this ability in quantum mechanics is not limited to just atoms either.

Complex molecules can be superposed.

Many have heard about many world interpretations verison of quantum mechanics. Very few have heard about many world chemicals that are capable of staying in superposition to deliver different possibilities and outcomes in Nature.

Physicists have now proven any chunk of matter can also occupy two places at once. Physicists call this phenomenon “quantum superposition,” and for decades, they have demonstrated it using small particles. But in recent years, physicists have scaled up their experiments, demonstrating quantum superposition using larger and larger particles.

The double-slit experiment reveals the central puzzles of the decentralized systems in quantum mechanics, putting us ‘up against the paradoxes and mysteries and peculiarities of nature”.

Researchers had long known that light, fired through a sheet with two slits in it, would create an interference pattern, or a series of light and dark fringes, on the wall behind the sheet. But light was understood as a massless wave, not something made of particles, so this wasn’t surprising. However, in a series of famous experiments in the 1920s, physicists showed that electrons fired through thin films or crystals would behave in a similar way, forming patterns like light does on the wall behind the diffracting material.

If electrons were simply particles, and so could occupy only one point in space at a time, they would form two strips, roughly the shape of the slits, on the wall behind the film or crystal. But instead, the electrons hit that wall in complex patterns suggesting the electrons had  interfered with themselves . That is a telltale sign of a wave; in some spots, the peaks of the waves coincide, creating brighter regions, while in other spots, the peaks coincide with troughs, so the two cancel each other out and create a dark region. Because physicists already knew that electrons had mass and were definitely particles, the experiment showed that matter acts both as individual particles and as waves.

But it’s one thing to create an interference pattern with electrons. Doing it with giant molecules is a lot trickier. Bigger molecules have less-easily detected waves, because more massive objects have shorter wavelengths that can lead to barely-perceptible interference patterns. And these 2,000-atom particles have wavelengths smaller than the diameter of a single hydrogen atom, so their interference pattern is much less dramatic.

To pull off the double-slit experiment for big things, the researchers built a machine that could fire a beam of molecules (hulking things called “oligo-tetraphenylporphyrins enriched with fluoroalkylsulfanyl chains,” some more than 25,000 times the mass of a simple hydrogen atom) through a series of grates and sheets bearing multiple slits. Recall cells are filled with porphyrins like the two below.

In the experiment in Cite #1, the beam was about 6.5 feet long. That’s big enough that the researchers had to account for factors like gravity and the rotation of the Earth in designing the beam emitter. They also kept the molecules fairly warm for a quantum physics experiment, so they had to account for heat jostling the particles.

When the researchers switched the machine on, the detectors at the far end of the beam revealed an interference pattern like we see with electrons. In fact, the molecules being studied were clearly occupying multiple points in space at once. This means large biomolecules can and do act like electrons do. They do have a superposed ability.

It’s an exciting result, for quantum biology, proving quantum interference at larger scales is possible. This was the first time in history this has been detected.

 

SUMMARY

The implications of this endogenous ability in chemicals is the basis of how MOLECULAR RESONACE operates. Molecular resonance is a quantum mechanical characteristic of all matter. This ABILITY is inherently BUILT into how REALITY is perceived. It is buried inside of the chemicals that cells have chosen to use through evolutionary timescales.

The most important biomolecules are coded for by DNA. DNA seems to favor biomolecules that have specific semiconductive and optical characteristics in their absorption and emission spectra. The design process of cellular life begins with the DNA code.   Centralized biology today is a detailed, disorganized collection of disparate facts. It is like a hoarder’s basement, or a rat’s nest. There is no decentralized connecting design of what is buried in DNA’s code. You can scoop up a bag full of facts and try to make sense of it, but that would be an exercise in futility. True wisdom is fractal and non linear. The design can be complex, with microscopic details, but the overall design is coherent and beautiful.  To make large collections of semiconductive proteins quantum coherent you need to link them together electrically.

We do this PHOTOELECTRICALLY.  This idea implies that cells have some electric tuning ability built into their protein structure.

It appears the choice is related to the spectrum of light that interacts with them. Possibilities and probabilities for life is made tunable just by changing the incident light photons. That is how these chemicals all operate. This implies that your mitochondrial metabolism creates an adaptable light spectrum during metabolism and it is this light that tunes and controls the chemicals in you to act in different ways.

A dopamine molecule consists of a catechol structure (a benzene ring with two hydroxyl side groups) with one amine group attached via an ethyl chain. The amine part of the ring contains nitrogen. If you draw the two possible Kekulé structures for benzene (pic below), you will know that the real structure of benzene isn’t like either of them. The molecular structure acts like it is capable of being in two states.

The two structures above for benzene’s ring are known as canonical forms, and they can each be thought of as adding some knowledge to the real structure. For example, the bond drawn at the top right of the molecule is neither truly single or double, but somewhere in between. Similarly with all the other bonds. The real structure is somewhere between the two – all the bonds are identical and somewhere between single and double in character.

Benzene two structures also sit in a superposed position. That’s because of the electron delocalization in the benzene ring. The aromatic rings of carbon in benzene are the playground for bio- photons as the picture below shows. Those benzene rings capture the photons and tune it.

As such, dopamine is the simplest possible catecholamine, a family that also includes the neurotransmitters norepinephrine and epinephrine.

If we take the two forms as the picture above shows perhaps the two most important ones, it suggests that there is delocalization of the electrons over the whole structure of the 6 carbon ring. With dopamine above, that electron density is a bit low around the nitrogen atom carrying the positive charge on one canonical form or the other. Any canonical form that you draw that shows nitrogen close to the ring, it follows that another atom must balance that charge. In dopamine that atom is oxygen at the 7 and 10 o’clock positions. Where the charge change occurs changes the absorption and emission spectra of dopamine. Separating negative and positive charges in this fashion is thermodynamically unfavorable. This is how tunability occurs with charge separation in a benzene ring. Light tunes molecules by altering their charges. This is why all the aromatic amino acids have benzene rings in their molecules. This also happens in methylene blue.

HOW DO YOU CREATE YOUR INNER MASTERPIECE?   YOUR CHOICES DICTATE THAT PATH

Dopamine controls the process of choice and action. Nothing EXCELLENT ever happens without EXECUTION. No masterpiece has ever been made by INTENTION alone. EXECUTION takes INITIATIVE and INTELLIGENCE. EXECUTION is the antidote to PROCRASTINATION. Ideation without execution leads to deletion of any idea. A poor idea executed accomplishes more than a great idea that stays locked away in a person’s head.  This blog is exploring how the small changes in light can affect change in your brain.  Actions end superposition. Actions – executions of ideas. EXECUTION calls off the fence of indecision and put us in the valley of decision; it calls us off the bench and onto the field. It does matter how much talent you have as a player in your life, but that talent is useless with inaction because you can never score a goal while you’re on the bench. That is how dopamine is the molecule of more for mammals.

This idea explains to us how dopamine can do all the things it is capable of doing without a lot of modifications we can observe biochemically. Dopamine drives you to seek out things far away, both physical, things you are blinded to, such as love, sex, wisdom, and power. Changing your ultraweal biophoton signature and shining it onto dopamine in certain circuits allows you to put hot sauce on your dinner, think about building rockets to fly to the moon, worshipping a God in the sky, beyind the space and time frames you live in. This chemical appears to have unlimited abiliities to bring to your life endless possibilities over any distance, whether that distance is intellectually or geographical. In your brain’s quantum computer, dopamine has become a single molecule that is the ultimate evolutionary handy tool. It is what moved us past Neanderthals, and began to urge us, through multiple tracts in our brains to move beyond the pleasure of just being, into exploring the cosmos of possibilities that come into focus when we imagine. Every creature on Earth has dopamine and melatonin in their cells, but no creature has more of them then humans. Madness and genius both depend on how dopamine is programmed by light. This tells you dopamine itself is capable of superposition. This idea also underpins this cliche as well. Talent hits targets no one else can hit; but genius hits targets no one else can even see.

I think this idea extends to chiral molecules in biology. DNA is made up of chiral molecules. Matter-wave diffraction patterns can put chiral molecules into superpositions of left- and right-handed forms. Experiments have already shown it and this will enabling new studies to be done of how the two states interact with their environment to give two different outcomes.

Small chiral molecules such as amino acids and sugars are the building blocks of larger molecules, such as proteins and nucleic acids, which are also chiral. A chiral molecule and its mirror image are called enantiomers; one is dextrorotatory (D) and the other is levorotatory (L). This is another way evolution likely happens that is also a break with Darwinism.

Most of you know I think this guy in the Tweet is a Twit when it comes to science. But even a blind squirrel is able to tell time correctly twice a day. Listen carefully what he says about Neanderthals and what I have told you about dopamine and creatitivity in this series already.

https://x.com/got_cake/status/1791306643809980457

Semiconductive quantum dots (QDs) have been widely used for fluorescent labelling in modern experiments. However, their ability to transfer electrons and holes to biomolecules leads to spectral changes and effects on living systems that have yet to be exploited in centralized science. Cells appear to do this easily.

How do I envision how this operates in us?

Quantum Dot-dopamine conjugates can be used to label living cells in a redox-sensitive pattern: under reducing conditions, fluorescence is only seen in the cell periphery and lysosomes. As the cell becomes more oxidized, Quantum Dot labelling appears mostly in the perinuclear region of cells. This would include in or on surrounding mitochondria where biophotons are created metabolically.

With the most-oxidizing cellular conditions, Quantum dot labelling throughout the cell is seen already in experiments. Thee experiments have taught us phototoxicity results from the creation of singlet oxygen, and it can be reduced with antioxidants. Melatonin is the major antioxidant inside the cell created by mitochondria to manage this process. there are many small molecule proteins liberated from mitochondria that could do this. When you comprehend what I am proposing here this picture below should have new meaning. It shows you how reality is perceived and how it can be changed rather easily. This explains how dopamine can build creativity, madness and genius in humans and how its creation can vary in one single life to explain what happened as Jimi Henrdrix, Kurt Cobain, or Jackson Pollack aged in their lives.

The living universe selects for maximum entropy, and minimum waste heat. Melanin was critical in evolution of bringing biological complexity to the interior of mammals.

In this context, the melanin universe in mammals can and should be seen as a self-organizing system that seeks to optimize its energy use and minimize waste heat. This is reflected in the emergence of complex structures and patterns in the universe, from the formation of galaxies and stars to the development of dopamine, and life on Earth.

The universe and cells have much in common. Both are decentralized systems.

The idea that the a cell and the universe are self-organizing systems that seeks to maximize entropy and minimize waste heat has far-reaching implications for our understanding of life and the universe and our place within it. It suggests that the universe is a dynamic and ever-changing system that is constantly seeking to optimize its energy use and maximize its complexity. It also suggests that tissues, collection of cells have the same ability buried within them.

Dopamine narrates your life and it is the main story teller of how life came to be within the primate clade in evolution.

CITES

1. https://www.nature.com/articles/s41567-019-0663-9.epdf

2. https://wires.onlinelibrary.wiley.com/doi/full/10.1002/wcms.1640

3. B. A. Stickler et al., “Enantiomer superpositions from matter-wave interference of chiral molecules,” Phys. Rev. X 11, 031056 (2021).

4. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285053/

The Melanin Renovation Rx is based on Noether’s theorem, which is the key missing piece. The theory states that every differentiable symmetry of the action of a physical system with conservative forces has a corresponding conservation law. The symmetry in the mammalian physical system is based on UV light. Time symmetry implies energy conservation. So, what happens to mammals when they lose energy? They lose time symmetry. In other words, time flows differently backward and forward. There was a time on early Earth that the TCA cycle only flowed counterclockwise because there was not a lot of oxygen or as much UV light around.

It sounds incompressible and unimportant until I remind you of what you just learned about the TCA cycle in the last few blogs. In modern times, biochemists are familiar with it running forward clockwise with plentiful oxygen and sunlight is pumped into the system every AM, and it rotates counterclockwise when these conditions are not met. The implications of this rotational symmetry change are enormous for you understanding. Why? Your time experience varies depending on the direction of the spin of this cycle in your cells. Sounds crazy doesn’t it?

Theories of criticality in physics have been successfully applied to biology. The mathematical core of these theories rests upon the idea that a “phase transition,” which can be either critical or not, may be described as a point along the line where the intended control parameter runs. For example, the ferromagnetic/paramagnetic transition of iron and oxygen takes place for a precise temperature value, the Curie temperature.

Remember that light and temperature control the entropy flow in your circadian clock mechanism. When you realize this, you might begin to see how people experience time differently in their lives

If you paid close attention to the video above, you’d have heard that energy conservation implies time symmetry. It also follows that anytime there is a violation of time symmetry, the energy conservation of the system has been violated in some fashion. This happens when mtDNA is altered, melanin is lost, or water is not created in cells from metabolism. All of these things change oxygen tensions inside of cells as a result. All these things cause our cells to liberate more light than we should. This light liberation changes the AMO physics in mitochondria. That is what the ROS and RNS signal tells the decentralized clinician. These ideas are all buried in the slide below.

What facts about Nature isn’t in the slide above? Most centralized scientist believe ROS is associated negatively with cell function. It just is not true. ROS is not inherently negative for cell function; instead, it plays a complex role in regulating various cellular QUANTUM processes that centralized biology has not stumbled upon yet. The interplay between ROS, endogenous biophoton creation, and low intensity laser creation inside of cells offers opportunities for the centralized audience to rethink their beliefs and approaches to understanding cell biology. Most of centralized science has no idea that cellular conditions involving elevated ROS production (chronic diseases like diabetes) are associated with increased low-intensity light therapy sensitivity. The reason is quite simple. Diabetic tissues have lost most of the sotred photonic energy at the electronic and vibrational levels in cells. Diabetic cells emit higher amounts of biophotons to their environment in an attempt to raise their own ROS to actually stimulate higher ATP production. The problem is oxygen tensions in diabetics is low, along with biophoton power and intensity so that endogenous light production for regeneration becomes improbable. The detection of biophotons is now well established in the biophysical literature, is also associated with the production of ROS and the cellular redox state. Low intensity light therapy via PBM which mimics what red light from the solar spectrum normally gives the semiconductors in cells. This light also has the potential to induce cellular effects through accelerated ATP production. This paper here: HYPERLINK should blow your socks off. When I read it in 2010 I was stunned.

Humans no longer live in the light this mechanism is designed to work with. This is a big part of why we have chronic disease epidemics that we do today. Few see how light is the driver of the entire process. By the time this blog is done, I think you will have enough data to show you why I am adamant that light trumps food at all the most critical levels in cells.

WHY DOES COLD HELP MAMMALS ALSO CONSERVE TIME?

When the temperature decreases and passes through that point, the magnetic orientation organizes along one direction, and magnetism appears. When the temperature increases through that point, disorder prevails, and magnetism disappears. Magnetism emerges from the system’s atomic-molecular organization. Think of mitochondrions as organelles that create paramagnetic chemicals (free radicals) by altering the atomic lattice of atoms fed into it. Most of the atoms fed into mitochondria are not paramagnetic. Many of the atoms that come from mitochondria have distinct magnetic fingerprints. Those fingerprints emerge from alterations of the AMO physics that are occurring inside the organelle.

Mammals’ criticality begins with UV light because it works with mtDNA, quantum dots, and melanin to create VUV-IR light inside a cell. When the critical amount of these entities goes missing inside mammals, they suffer a loss of healthspan or a loss of time. Their TCA cycle does not spend most of its time spinning in a clockwise fashion. When they get enough AM light, and sunlight during the day, they become robust and antifragile because the TCA cycle is operating as it should. When they do not, they get sick and die sooner than they should.

The TCA cycle highlights this time symmetry idea. The same biochemical pathway is used to create and destroy cells. I have told you many times that everything can and should be thought of as a clock. That is clearly how Nature views the TCA cycle when you view it from this perspective.

Very recently in this series of blogs I told you about an experiment in 2012 that showed us that the laws of physics are not time symmetric. It was buried from most people’s awareness because the experiment occurred at the same time the Higgs boson was discovered. Prior to this 2012 experiment, centralized science believed, that whether you run “a clock” forward or backward, most believed the laws of physics to be the same because of Noether’s theorem. The 2012 experiment showed us otherwise and I became quite happy because it explained to me really what the TCA cycle was doing and why mammals lose light when the TCA cycle is spinning counterclockwise. During this shift in time, we should expect a change in energy based on the relationship of conservation laws to time time symmetry. That was the point of showing you the video above. The TCA cycle is a cell’s difficulty adjustment in how it tells time. I want you to understand that when time is the currency in question, energy has to be expended and it is lost to the environment. When this happens aging manifests. This is truly how time is created in biological systems based on a proof of work mechanism.

This concept of time is funda­mental to our way of thinking. It is derived from the more basic concept of the order in which events occur. Given the perspective I am trying to show you, I want you to ask yourself the following questions. Who or what should be in charge of time if putting someone in charge is not allowed in the system? How can you have a reliable clock if there is no central frame of refer­ence? The key here is to understand in your cell, a mitochondria is the time machine that houses this TCA clock. That TCA cycle mimics a difficulty adjustment in the cell. Can I just make energy or do I have to make things I need to operate my cell? Got it? How that clock works is based on how often it senses the sunrise in its environment. I have brought this message to social media for 20 years.

AMO PHYSICS INSIDE OF THE MITOCHONDRIA IS CRITICAL

This criticality of this idea scales and corresponds to the appearance of a “coherent structure” in mammalian cells, that is, space and/or time correlations at all scales, which at the transition point (melanin renovation point) give a “global” aspect to the new physical object. These ideas are pretty relevant to analyzing quantum actions buried within biological organisms.

Melanin is critical in maintaining the AMO physical organization of the mitochondria and the functioning of the TCA cycle. Why? Melanin is only translated from its parent gene when UV light is present in the mammalian environment and or its tissue. This point cannot be magnified enough of how critical this relationship is to light. No other gene is linked to smallest part fo the visible spectrum of the sun and this same frequency of light is linked to every single biophoton cells release. It is a remarkable connection in nature that has gone unnoticed by centralized science.

Biological systems, on the other hand, exhibit criticality across multiple parameters such as genetic variations, environmental changes, and interactions with other organisms. This ongoing criticality allows for flexibility and adaptability in response to changing conditions, ensuring the survival and evolution of the organism.

Furthermore, the concept of criticality in biology extends beyond individual organisms to entire ecosystems. Ecosystems are complex networks of interacting species and environmental factors, and their stability and resilience are maintained through a delicate balance of interactions. When this balance is disrupted, it can lead to catastrophic shifts in the ecosystem, such as species extinctions or ecosystem collapse.

Overall, the concept of criticality in biology highlights the dynamic and adaptive nature of living systems, and underscores the importance of studying and understanding the complex interactions that govern biological processes. By recognizing and studying critical transitions in biological systems, we can better understand how organisms and ecosystems respond to environmental changes and potentially develop strategies for conservation and management.

Circadian control in a tissue is an ideal example of how biology builds its most important criticality.  Its efficiency is correlated with mitochondrial redox power between -440meV to -200MeV.  Outside this “critical” zone, life has problems.  Without the maintenance of this redox zone, the clock within the time machine is altered, and mammalian health metrics fall apart.

I submit to you that both of the pictures above are showing you Nature’s recipe for time buried in living systems. The first picture you are well acquainted with if you are a scientist. The second one is for mathematicians which also shows how light time shifts mammalian longevity.

Life solves this problem by re-inventing time itself. It says no to seconds and yes to mitochondria to create its own version of biological time stamping in cells. All clocks rely on periodic processes, something that we might call a “tick.” Mitochondrial periodicity is linked to AM sunrise and this begins the “tock” that clicks in the TCA cycle. The frequency of your clock — how often it ticks — depends on its use-case with the light choices you make. Your clock is an atomic optical lattice clock.

Most clocks you are familiar with have a fixed frequency. After all, we want to know the time precisely when we are going to a meeting or a class. There are, however, clocks that have a variable frequency. Your circadian clocks are based on the variable frequencies of how the sun changes in a day. Those clocks are called metronomes. A metronome has a variable frequency that you can set before you make it tick. While a metronome keeps its pace constant once it is set. This is why AM sunlight is irreplaceable in humans. It sets the pace for the TCA cycle. This makes the TCA act like a difficulty adjust knob in the clock.

While time causality is essen­tial in biochemical pathways, it is not suffi­cient to explain biological time keeping. This is why we have molecular clocks. They focus on time causality. The more counterintuitive reality of timing in the mitochondria is that they need unpredictability to work well. Why do we need two ways of handling time? It turns out we need unpre­dictability for time to flow for our quantum realm in cells. In the physical realm, we observe natural processes to describe the flow of time. We observe a general increase in entropy and call that the arrow of time. Even though the laws of nature seem to be obliv­ious in regards to the direc­tion of this arrow in most cases, certain things can’t be undone, practi­cally speaking. You can’t unscramble an egg, for example..

Similarly, entropy-increasing functions are required to estab­lish an arrow of time in the quantum realm in mitochondria where subatomic particles are being used for timing. Just like it is practi­cally impos­sible to unscramble an egg, it is practi­cally impos­sible to unscramble the epigenetic signa­tures that control the genome. When timing is off in your mitochondria that is precisely what happens to your DNA and that is what causes genomic shifts in cancer.

In biology, the proof-of-work mechanism is physi­cally linked to what happened directly with the sun that day. It is not just a record of an event — it is the event itself.

Without this controlled increase in entropy in cells, we could go forward and backward in time without consequence. Cells rely upon two sources of unpre­dictability: biochemical reac­tion times and the proof-of-work mechanism in sunlight’s energy. Just like nobody can predict what your Twitter feed will look like tomorrow, nobody can predict what the next human offspring will look like in the future either. This is what powers evolutionary change. This is how biological timestamping operates. It is not the world Darwin saw. It is a quantum mechanical process that uses light to create a ledger of time we call life. How is that for a new way to look at yourself?

SUMMARY

In a mitochondria, all we have is subatomic particles which contain data from our environment. It should follow then, that the biological realm is infor­ma­tional in nature, the obvious conclu­sion is that compu­ta­tion is all we have. If your world is made of data, manip­u­la­tion of data is all there is. This is why Nature built a mitochondria after endosymbiosis. She needed a time machine to make complex life.

Proof-of-work works in Nature-to-cell setting because it is trust­less, and it is trust­less because it is discon­nected from all superfluous inputs — such as the readings of clocks, food, your family’s opinions, or the narrative of social media. It relies on one thing and one thing only: compu­ta­tion requires work, and in our universe, work requires energy and time. The brilliant thing about cell biology’s proof-of-work mechanism is that it creates its own reality, along with its own space and time.

Einstein proved time is relative, and simul­taneity is nonex­is­tent. This fact alone makes all timestamps — especially across large distances like we have in biology — inher­ently unreli­able. This is why the SCN needs to be time stamped every morning by AM sunlight. It is also why your iPhone needs to update its GPS coordinates to work. It also explains fully why timestamps of GPS satel­lites have to be adjusted constantly, by humans on the surfaces of Earth to make tech gear operate properly. For life, biological timestamping has to be very precise to maintain health. If it is not chronic disease is the result. This is why evolution built the TCA cycle to function in spontaneous fashion. See Nick Lane’s picture below. Nick still has not figured out why Nature did this.

The reason was simple. Life has to be costly in time and not in energy. The TCA cycle is the diffi­culty-adjust­ment in cells. It’s evolutionary function is about keeping a constant time in cells, not a constant level of immunity in all tissues or in energy expen­di­ture. We know the TCA cycle varies its energy production in various tissues. Using the TCA cycle spin was an ingenious early step in evolutionary design because longevity has to be costly in time, not energy. Time is the most valuable asset in Nature because it has a fixed quantity. Energy can be sourced in many ways quantum mechanically by cells. if you are understanding this blog well now, Noether’s theorem says that energy conservation is LINKED to time symmetry. This means that every improve­ment in energy gener­a­tion in cells over evolution would allow life to create time. Time is the only thing cells cannot make more of. They became able to build complexity because they began to harvest more energy from the environment. That is what the picture above Nick’s head really says, but Nick is yet to realize it. I hope you do now too.

Nick Lane is correct that understanding why the TCA cycle underpins life is a great mystery to be solved. I am giving you my solution in this blog. It has been in my head for 20 years. The TCA is the biological diffi­culty adjust­ment life needs because it is essen­tial as some of the amino acids its uses.

Because, without it, the internal clock of mitochondra would tend to go faster and faster as more biochemical pathways join the biological network in cells. It would speed up biosynthesis pathways we use to create offsprings via sex. We would quickly run into the coordi­na­tion problem that mitochondria was built to solve as evolution’s time machine. Cancer is this coordination problem. This is why light stress increases ATP production. ATP production is telling us something about the NAD+ to oxygen difficulty adjustment in mitochondria. Something is awry in our quantum timing mechanism. This story goes way back in the blogs. Don’t believe me? READ IT.  Note the date. The ideas in that blog began in my head in 2000-2004. You likely never saw it this way before today.

By viewing living entities as extended critical transitions, we can see them as dynamic systems that continually renew and adapt their structure. This perspective allows us to understand the complexity of biological processes in a new light, recognizing that they are not just static phenomena, but rather evolving and changing systems. This can help us overcome the challenge of analyzing the intricate and nuanced nature of living matter, providing a framework for studying and understanding biology in a more interconnected way. This is the idea buried deep in the QUILT document.  Ultimately, this change in perspective from physics to biology offers new insights and approaches to unraveling the mysteries of life.

There is a very common belief in humans in a divine force or energy that gives life to all living beings has been prevalent throughout human history and has shaped the way we view life and existence. It has provided a framework for understanding the purpose and meaning of life, as well as guiding moral and ethical behavior.

The concept of life as a gift from a higher power has been a source of comfort and hope for many people, offering a sense of purpose and belonging in a vast and often mysterious universe. It has also served as a basis for the belief in an afterlife or continuation of the soul after death, providing solace in the face of mortality.

While the scientific understanding of life has evolved and advanced over time, the religious and spiritual concept of life as a divine gift remains a powerful and enduring belief for many people around the world. It continues to shape our values, beliefs, and behaviors, influencing how we live our lives and how we view the world around us. Ultimately, the concept of life as a sacred and precious gift reminds us to cherish and respect all living beings, and to strive for a more harmonious and interconnected existence.

Some argue that the theory of evolution through natural selection contradicts the second law of thermodynamics, which states that entropy, or disorder, in a closed system will always increase over time. They claim that the complexity and organization seen in living organisms goes against this principle, as it suggests a decrease in entropy rather than an increase.

However, proponents of evolution point out that the Earth is not a closed system, but receives energy from the sun, allowing for the increase in complexity and organization seen in living organisms. They argue that the second law of thermodynamics applies to isolated systems, not open ones like the Earth.

Ultimately, the debate over evolution and thermodynamics continues to be a contentious issue, with both sides presenting compelling arguments. However, many scientists and scholars maintain that there is no inherent contradiction between the two concepts, and that they can be reconciled within the framework of modern scientific understanding.

As yourself this question: Is life a property of matter that does not naturally exist? Might life be a phase of matter that we invented with the help of the environment. On the most fundamental level, all matter that exists is just an arrangement of atoms and their constituent particles, is it not?

This perspective challenges the traditional notion of life as a distinct and separate concept. Instead, it suggests that life is simply a human construct used to categorize certain arrangements of matter. This mindset can lead to a greater appreciation of the interconnectedness and complexity of the universe, blurring the lines between living and non-living entities. It invites us to question our assumptions about what it means to be alive and opens up new possibilities for understanding the nature of existence.

Are mammals/humans, for instance, a bag of special water filled with 26-element human molecules that has been synthesized, by the operation of universe, over the course of the last 13.7 billion years? Or is this something more to this reductionist view point?

Living entities are not “just” processes but something more: they are lasting, extended critical transitions, always transient toward a continually renewed AMO structure. In general, physical processes do not change fundamental symmetries; to the contrary, they are primarily meant to preserve them.

Living organisms exhibit emergent properties (quantum mechanical) that cannot be fully explained or understood by simply breaking them down into their molecular components. The photomolecular effect is one example. These properties arise from the interactions and relationships between molecules and cells, and they give rise to the incredible diversity and complexity seen in the natural world.

Therefore, while it is important to recognize the fundamental chemical and molecular basis of life, it is also crucial to appreciate the complexity and emergent properties that make living organisms more than just the sum of their parts.

From Nature’s view, the world should be seen as only connec­tions, nothing else. Everything is based on probability and nothing is based on cause and effect. This is the perspective of this decentralized quantum biologist.

^^^^This is cite #7.

CITES

 

1. Principles in Geology, by Charles Lyell, 1868.

2. The Origin of Species, by Charles Darwin, 1859

3. http://www.staroceans.org/e-book/Haber_Stornetta.pdf

4.  https://www.math.columbia.edu/~bayer/papers/Timestamp_BHS93.pdf

5. https://medium.com/codex/power-of-merkle-trees-1e44819e9639

6. https://stephanlivera.com/episode/313/

7. https://www.nature.com/articles/s43587-024-00619-x4