When humans began using the alien portion of the electromagnetic spectrum along with the blue light on every screen in tech gear everywhere is when the obesity curves turned. It was not the food as the slide below shows. 1980 is when TV use really became explosive for color TV and 1995 was when technology spending took off and it created computer screens and terminals.
It was light and that light ruined how mitochondria could or could not handle food electrons and protons in mitochondria. Leptin resistance causes obesity. Leptin resistance = LR. LR = low melatonin because of melanopsin dysfunction. This story should not shock the older members in here but yet again you guys surprise me. Where was leptin found? Subcutaneous fat in 1994 at Rockefeller University.
Where does leptin have to go to tell the body about energy balance according to the old leptin blogs? The hypothalamus.
What connects the two?
Light connects them.
The light you choose, and not the food you eat. Food out of season from the control of photosynthesis is a problem but nothing compared to the light your eye and skin observe and measure.
A lack of full-spectrum solar exposure during the day, or getting man’s light at night is the most common reason for disease epidemics today, and in my opinion, the most overlooked issue in all of medicine these days. When blue light, RF, or microwaves affects melanopsin adenosine biology is altered. This is how adenosine rises and it is when melanopsin receptors are recycled.
Proper ocular melatonin cycling requires that these two frequencies (UV/IR) be present in the AM to stimulate the regeneration processes in the eye during the daytime. This quantized process also requires ABSENCE of blue/green light between 400-560nm post-sunset!!!! When these things are off the result always = INFLAMMATION = too many protons (deuterium) and/or not enough electrons at the mitochondrial cellular level = lowered melatonin levels in the eye, brain, and blood plasma.
The same is now true in the skin and subcutaneous fat because melanopsin is there now too. The same thing is true about our arteries. That is how leptin resistance occurs at the tissue level. Melanopsin dysfunction turns retinol into a “time bomb”. That time bomb is a disease. Free retinol destroys melatonin and DHA atomic lattice in tissues. This RUINS the band gap conduction in tissues. Diseases cause you to lose time and a loss of time is because tissue level entropy is increasing.
Moreover, that time bomb ruins the aromatic rings in melanopsin, leptin, and melatonin to ruin their ability to communicate with the hypothalamus to give accurate light/time information about energy balance because information quanta are LOST to the colony of mitochondria in that tissue.
Life is designed to be as predictable as a pair of dice and this is why eukaryotes used viral parts and then stole a bacteria and turned it into mitochondria. It allowed cells to make better predictions using excited electrons, protons, deuterium, and diurnal and seasonal solar light changes to gain that stability by organizing cells to remain far from equilibrium.
Anytime you slow light down with an interaction with matter in a cell your cells become capable of slowing time or losing time and creating and changing a living system. (Vermont video 2017)
Biochemical FLUX is explained by LIGHT: How does the enzyme know where the substrate is? It follows the path that light left in its wake. That pathway is made by excited electrons that leave the lattice and move within the electron clouds because light only interacts with electrons. Enzymes all work by proton tunneling. Red light is what moves things with mass. Protons have 1836 times more mass than electrons. Light moves electrons by exciting them photoelectrically.
Protons work differently with light. Red light moves things with mass, so the mass of the proton and red light’s ability in a cell are yoked to circadian signals inside a cell. So the pathway where a connection needs to be made between two chemicals or atoms in a cell will be lined with protons and neutrons in our protein lattice. It is almost like having a canyon carved into the cell for running water to follow.
In this analogy, the running water is the light that the cell assimilated, harnessed, and frequency adjusted in some way. Cell water does not equal tap water. Cell water is equivalent to water in our blood plasma. This means the type of protons in water matters deeply to a cell. Blood has more deuterium in it than cell water does for a quantum mechanical reason. It creates the UVC light that leptin needs. This is why cell water is capable of acting as a molecular mirror (Vermont 2018 talk) for the 42% of infrared-A light in terrestrial sunlight.
Therefore, the enzyme gains knowledge of the path it should take because light leads it to its partner molecule. This happens are lightning-fast speeds (atto or femtoseconds) because the interaction between light and electrons is instantaneous. This means an enzyme knows the path through “a quantum observation’ of the system dynamically, of course.
The enzyme, a protein, has alpha helices that absorb light in specific spectral frequencies. That is what semiconductors do. Those helices are tuned to the frequency of the substrates. Infrared spectroscopy demonstrates that each organic molecule has its own unique signature. Amazingly, the alpha-helices are just the right size coils to be easily tuned to the entire infrared and visible spectrum. The enzymes often organize as dimers for depth perception, just as we have two eyes.
THE BASIS OF THE LEPTIN Rx WAS ALWAYS LIGHT BASED
Your body is a collection of semiconductors that DNA has magnetically stored in our nucleic acids. Those semiconductors only work with visible light. Melanopsin, retinol, melatonin, and leptin are all biological semiconductors. How does it work Jack?
Leptin induces two major effects on cells and their mitochondria by triggering a photonic signal transduction cascade: enhancing mitochondrial biogenesis and activity as well as enabling cell propagation and differentiation. The janus kinase-dependent signal transducer and activator of transcription 3 (STAT3), the adenosine monophosphate kinase (AMPK), and the peroxisome proliferator-activated receptor gamma coactivator (PGC)/peroxisome proliferator-activated receptor (PPAR) pathways are converging in supporting mitochondrial function and cellular proliferation.
The diversity of leptin-dependent signaling in the skin is illustrated by the fact that the hypoxia-inducible factor-1α, which controls the expression of multiple different genes, including that of key regulators of angiogenesis and wound healing, is also upregulated by the action of leptin.
THE PHYSICS OF LIFE IS LINKED TO COLOR
The color of absorbed and emitted light both depend on the band gap of the semiconductor. Visible light covers the range of approximately 260-760 nanometers. This corresponds to 1.8-3.1 eV (electron volts). The color of emitted light from an LED or semiconductor laser (LED) corresponds to the band gap energy and can be read off the color wheel shown below.
So consider the color of the human liver. It is the source of where gluconeogenesis or animal photosynthesis occurs in us. The liver is reddish-orange/brown when it is not diseased. The liver has this reddish orange because it has a lot of Iron oxides and this color confers has a 2.2 eV band gap. Now look at all the other things distal to the liver in the gut which relies on the band gap present in the liver being accurate as we live. In diabetics, it is destroyed. Diabetes is essentially a narrow-band gap disease.
The color of absorbed light in semiconductors includes the band gap energy, but also all colors of higher energy (shorter wavelength), because electrons can be excited from the valence band to a range of energies in the conduction band. Thus semiconductors with band gaps in the infrared range appear black because they absorb all colors of visible light. Nothing in humans truly is black. So this tells you in human biology nothing absorbs all colors of visible light from the sun.
They use parts of the spectrum of the sun to communicate information to drive physiology. This means the spectrum of life we live under is critically important. Skin and eye MDs tell us the sun is toxic yet modern humans do not live under that light, do they? And they get modern diseases that were rare before manmade light was created in 1893.
The band gap is a very important property of a semiconductor because it determines its color and conductivity of the semiconductor. Many of the applications of semiconductors are related to band gaps:
- Narrow band gap materials are used as infrared photodetectors and thermoelectrics (which convert heat to electricity).
- Wider band gap materials are used in electronics, light-emitting diodes, and solar cells.
- Biological systems use both. Bone for example is a wider band gap semiconductor. Cytochrome C oxidase is a narrow band gap semiconductor that creates water by converting mitochondrial heat and light emission.
To be clear let us go back to the liver to explain how color and conduction bands and light link. The liver has a band gap of 2.2 eV and thus absorbs light best at a λ < 560 nm. It thus appears reddish-orange (the colors of light reflected from Fe2O3 because the semiconductors in the liver absorb green, blue, and violet light best. It reflects most of the red and orange colors. Those colors are the most dominant parts of sunlight but aren’t as useful to the cells in the liver. Hepatocytes have a specific atomic lattice to do the things a liver does.
Hepatocytes are dissipative structures in the liver, but not the only ones. They transform light energy and create order from the disorder in light they use to operate. When things are broken down in the liver non alcoholic fatty liver disease manifests as a result.
Dissipative structure theory (Prigogine) led to pioneering research in self-organizing systems, as well as philosophical inquiries into the formation of complexity on biological entities and the quest for a creative and irreversible role of time in the natural sciences. This is why circadian timing is the critical factor in the Leptin Rx.
There is a well-known theorem of minimum entropy production derived by Ilya Prigogine, which states that entropy exported from a system reaches a minimum, or becomes zero, at thermodynamic equilibrium. Prigogine’s theorem is a direct consequence of Onsager’s reciprocity relationship. The principle of internal entropy compensation implies the principle of minimum entropy production, which is valid in dissipative structures built far from thermodynamic equilibrium.
WHAT IS ANOTHER DISSIPATIVE SEMICONDUCTOR IN US?
Hemoglobin is a porphyrin protein. Hemoglobin has a specific absorption spectrum. Porphyrins are semiconductors in living systems.
The most common examples of porphyrins are the heme proteins found in hemoglobins, myoglobins, P450 enzymes, cytochromes, catalases, peroxidases, chlorophylls, and bacteriochlorophylls.
The porphyrins are heterocyclic ring structures that include four pyrrole rings joined together through carbon (methenyl) bridges. The most abundant porphyrins in nature are found in hemoglobin and chlorophylls. In the center of porphyrins, a metal atom is chelated to the nitrogen atoms of the pyrrole units.
Whole blood has absorption maxima at 545 and 578 nm, as has been previously reported in the literature in cite 3 below. Hemoglobin is a semiconductor that has an isosbestic point. It has two forms oxyhemoglobin when it is carrying oxygen toward mitochondria and deoxyhemoglobin when it is carrying blood away from mitochondria back to the heart and lungs. An isosbestic point is observed in overlaid spectra when a chromophoric precursor is converted to a product with a different spectrum so it is often assumed that an isosbestic point occurs only when the precursor is quantitatively converted to a single product.
Isobestic points are used in medicine in a laboratory technique called pulse oximetry to determine hemoglobin concentration, regardless of its saturation rate of oxygen. Oxyhemoglobin and deoxyhemoglobin have isosbestic points at 590 nm and near 800 nm. RBCs are red because oxy-Hemoglobin does not absorb any light above 600nm. Hemoglobin makes up 94% of the mass of RBCs but RBCs do not work unless they are in the water. Blood is 93% water. Because of the atomic organization inside of cells (AMO physics) there is always light energy stored and available within the cell system. This is how entropy is limited in cells. This is the basis of what a dissipative structure is doing at the smallest level.
When sunlight hits RBCs a net negative charge forms adjacent to the RBC membrane in blood plasma (pic above). The energy derived from the sun is stored coherently in the RBC and in the water it floats in, and is ready for use, over all space-time domains present in tissues. Mitochondrial water production is critical in life’s semiconductive blueprint because porphyrins in cells bind iron, and carries oxygen to our colony of mitochondria in organs and tissues.
Mitochondria create water, CO2, and heat.
The fidelity of this water creation is the basis of the autonomy of organisms. Organisms are never simply at the mercy of their environments on account of the coherent energy stored. When the environment steals this ability from cells (nnEMF) cells are at the mercy of food and exercise. When you get enough sun food becomes less necessary. Everyone’s system is set differently because our semiconductors do not have the same band gaps based on genetics, skin color, eye color, haplotype, latitude, or atomic lattice arrangement.
More to the point, we don’t have to eat constantly (Leptin Rx above) when we’re in the sun, leaving plenty of time for other useful, pleasurable activities (SEX) that lead to the next generation of life. This is the evolutionary directive. Leptin also controls fecundity in us. All sex steroid hormone pathways in humans are filled with POMC neurons that create melanin. This means sunlight, also controls fertility. I believe because of melanin, the UV part of the spectrum is the most important part of fertility. This explains why so many young people are infertile today.
WATER IS ALSO A SEMICONDUCTOR
Light absorbed by RBCs changes the atomic/physical structure of the water surrounding RBCs and we can see this change when we see the charge around RBCs that have been irradiated by light.
The other consequences are that the organism is exquisitely sensitive and free from the mechanical constraints of life on Earth; and satisfies, at least, some of the basic conditions for quantum coherence. Water provides those abilities as well.
Liquid water on Earth is quantum coherent even at ordinary temperatures and pressure. This is why Nature got the idea to build cells around liquid water. It functionally is a naturally formed quantum computer. Liquid water made in the mitochondrial matrix is the most wonderous chemical Nature has ever built because the water forms more coherent domains than the water from the hydrology cycle.
Even latitude variation shows how water homogeneity changes as solar inclination affect its molecular arrangements and bond angles in hydrogen in water. Mitochondrial matrix water associates with macromolecules and membranes in cells into a gel-liquid crystalline configuration that enables enzymes and nucleic acids to function as quantum molecular machines that transform and transfer solar energy at close to 100% efficiency.
Liquid crystalline water at interfaces also provides the excitation energy that enables it to split into hydrogen and oxygen in photosynthesis, simultaneously generating electricity for intercommunication and for the redox chemistry that ultimately powers the entire biosphere on the 3rd rock from the sun.
Water is the means, medium, and message of life and it has to be made in large quantities in your mitochondrial matrix for you to remain healthy. Any reduction in its production will lead to some diseases.
SOLID STATE BIOLOGY IS MELANIN-LEPTIN Rx SPECIALTY
How do semiconductors handle a variable spectrum of light in physics?
Increasing the mole fraction of the lighter element (than the semiconductor atom) results in a larger band gap, and thus higher energy of emitted photons. This is how ELF-UV frequencies are controlled in cells. It is also how mitochondria vary light emission in cells to inform DNA what to do.
EMFs in mitochondria inform DNA what to do. DNA signal organelles how to arrange atoms in cells to store energy by molecular resonance. Leptin evolved to control this process in your cells. Light coming through your eyes and skin begins the process.
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.
To understand the last sentence you must understand what semiconductors really do. Why do they have certain colors and what controls their ability to conduct electricity and create light for optical signaling in cells?
Pure (undoped) semiconductors can conduct electricity when electrons are promoted, either by heat or light, from the valence band to the conduction band. The promotion of an electron(e-) leaves behind a hole (h+) in the valence band. The hole, which is the absence of an electron in a bonding orbital, is also a mobile charge carrier, but with a positive charge.
The motion of holes in the lattice can be pictured as analogous to the movement of an empty seat in a crowded theater. An empty seat in the middle of a row can move to the end of the row (to accommodate a person arriving late to the movie) if everyone moves over by one seat. Because the movement of the hole is in the opposite direction of electron movement, it acts as a positive charge carrier in an electric field or magnetic field.
This solid state physics lesson above taught me to look at the choroid in the human eye to learn something about the future risk for obesity. This is when I began to get interested in OCT of the retina.
The opposite process of excitation, which creates an electron-hole pair, is their recombination. When a conduction band electron drops down to recombine with a valence band hole, both are annihilated and energy is released. This release of energy is responsible for the emission of light in LEDs. This is how light is created in cells to make ultraweak UV light spoken about in this book below.
UNDERSTANDING BIOCHEMISTRY IS NOT ENOUGH IN A BLUE-LIT 5G WORLD
Alchemist & Metaphysician = ancestral beliefs that biochemistry in a textbook is the definitive science of how life operates. This is myopic. In 2023, n fact, it is pure BS. Biochemistry is really a solid-state story of light and hydrated semiconductive proteins that change their ability as the electromagnetic signals on their surfaces, and this is capable of changing the geometry in their lattice via a change in charge density. All this is done epigenetically by light.
People forget that Einstein taught all of science that light and time are relative. This means that food is also relative to the time of the day, but the implications of both are not obvious to those who have not that deeply about it. Once you do you’ll understand nature better.
For example, the great thing about telescopes is that they are time machines. Because light travels at a finite speed When we look up at stars we see how the light was in a previous time. The great thing about microscopes is that we can see how time elapses because the speed of light within a tissue varies and is reflective and instructive to our perceptions.
Do you look “at science” or do you look thru science through a lens? I submit that most of us are prisoners to modern science perspectives because we see it via “their lenses”. People who only understand biology via the biochemistry we know are people I avoid. I look at nature and turn it 90 degrees, 180 degrees, 270 degrees, and degrees in between. This is what quantum mechanics requires us to do. Every time I do this, my perspective of a problem changes and I learn a little bit more about what I missed from the fundamental view from which I was taught.
I learned to do this from DaVinci and Michelangelo who were masters of altering the ground and foreground in their works. They changed the sizes and shapes of proportions in their art to make the visualization of the observer more lifelike. They were masters at altering the lens that we see the world through to make it more accurate based on where we were in space and time I view science in the same way. I need to alter the perception of what we currently believe so you can see the parts of science that are unobservable in action. Just because you can’t or don’t see it does not make it immaterial.
On the contrary, it turns out that what you can’t see and do not know are the most important parts of science. Do you look at that lens and observe how it might bend reality? You should because this is the mitochondriac way.
IMPLICATIONS OF THIS LIGHT LESSON
The mass of a body and its direction varies with the surface electric charge it contains. Since RF radiation induces massive surface charges we should have expected the obesity crisis during the technological revolution but we did not because we do not understand how the physics of cells are disorganized by nnEMF. When you add in what microwaves do to bonds and their angles it should be no surprise what melanopsin and retinol damage would do to things like leptin in the skin, blood vessels, and subcutaneous fat, but most people are small thinkers.
Choroidal Vascularity Index is novel parameter for Optical Coherence Tomography (OCT) and the earliest marker I know for oncoming obesity.
The paradigm in control of the truth only believe the fuel input affects the obesity quotient in the system because they do not understand the amazing nuance in how light works inside our cells. This implies that the addition or subtraction of light changes the charge of our cells and tissues, and thusly affects our BMI. In 1998, we found melanopsin in the eye. This is when I realized that when blue light hit the eye some part of the retina had to get larger. I looked for the answer and I found it. (pic below)
I knew that some parts of the eye would be losing light energy and have to get larger as a result before the same process happened in the body. The picture below is of a choroid that got larger before a shift worker gained 30 pounds in 4 months. Melanin-leptin biology ties to the semiconductive circuit in the central retinal pathways.
The choroid gets fatter/thicker before your waistline does. The physics of light told me that and now the literature has that proof for you to examine.
Until recently, the choroid’s inaccessibility—essentially buried beneath the retina—has made it a little understood anatomical structure. But this thin layer between the sclera and the retina, the “middle coat” of the eye, is vital to ocular health. It supports the outer layers of the retina by supplying nutrients and removing waste. Choroidal melanocytes absorb intraocular scattered photons (light). The superfluous flow of blood through the choroid assists in the removal of heat derived from the metabolism of phototransduction. Also, the suprachoroid lamina provides a safe route of travel for the long posterior ciliary arteries and nerves as they course toward the anterior aspect of the globe.
Choroidal analysis, in addition to retinal imaging, can provide supplemental information regarding disease progression. The thickening of the choroid is the first step in human weight gain. The thinning of the choroid is an indicator of myopia with advancing stages of non-exudative age-related macular degeneration (AMD). This then correlates with the rate of visual field loss in eyes with normal tension glaucoma (NTG).
In healthy eyes, the choroid is typically thickest beneath the fovea, where its average thickness ranges from 262µm to 354µm. The surrounding superior and inferior choroidal quadrants within the macular region are generally thicker than the nasal and temporal quadrants. The temporal choroid is thicker than the nasal choroid, which decreases rapidly toward the optic nerve. This is important when one considers the somatotopic organization of the melanopsin system in the eye linked to the RPE. It is also different and organized around how the visible light spectrum bends in the eye. Generally, the superior choroid is thicker than the inferior choroid. The choroid tends to be thinner where melanopsin photoreceptors are located. This thinning of the inferonasal macular choroid marks the location of the embryonic optic fissure of the diencephalon and likely represents a normal “relative coloboma area”.
Additionally, the thinning of the choroid between the fovea and the optic nerve may predispose the formation of peripapillary atrophy. In the optic nerve, the peripapillary choroid is thinnest inferiorly and may contribute to the pathogenesis of glaucoma in susceptible cases of myopia. Below is an enhanced depth choroidal image of a normal eye, a function of optical coherence tomography (EDI-OCT).
Above is a Gray-scale EDI-OCT of a healthy eye. The white arrows correspond to the choroid/scleral junction.
EDI was pioneered by ophthalmologists Ron Margolis, MD, and Richard F. Spaide, MD, in 2009. Before their work, OCT imaging of the choroid was virtually impossible because of poor light source penetration through the densely pigmented retinal pigment epithelium, light scatter by the choroidal vasculature itself, limited axial resolution and motion artifacts. Today, we can obtain an OCT with a simple push of a button.
Today, we’re able to image deeper into the eye than ever before, allowing us the opportunity to evaluate choroidal thickness and morphology both for the benefit of patient treatment and for a better understanding of retinal diseases.
That is where I believed obesity began until December 2017. As of December 2017, new data showed melanopsin is also in the skin, subcutaneous fat, and arterioles below the skin and retina I know it can come from damage from either tissue today. Is the final story cast for me today? Nope. I have more expectations that melanopsin is going to be in other places too that explain diseases today medicine is clueless about.
Explaining how it all works is complex as the picture above and below show.
The collateral damage depends on how melanopsin was damaged and what other parts of the electromagnetic spectrum did the damage. This implies obesity is dynamic with respect to light damage too. Everything is relative in life and humans are too myopic to see this perspective.
FOR EXAMPLE: Can a simple blue LED light from a cell phone cause carbon-nitrogen (CN) coupling using copper in you? Yep. Researchers found that “blue light was able to start the photoreduction of a substrate to form an alkyl radical via electron transfer.”
Carbon nitrogen coupling is the most common bonding atoms in all of biochemistry. Do you still think you’re immune to all those LED’s TV’s, iPhones, screens, and iPads? If so, Mother Nature is chuckling at your arrogance, if you do.
And if you’re not arrogant about your technology use you are likely quite ignorant of the power of blue light to uncouple your cellular architecture in mitochondria and cells to give you diseases you cannot fathom that are linked to this interaction. ALS, PD, myopia, AD, cancer, heart disease, and diabetes. Yep, every disease you can think of is affected by this. It is time to upgrade your knowledge about light. HYPERLINK
^^^^The most honest accurate assessment one should have based upon where the science is pointing us in 2023. Your job is to know this is the way you need to be thinking.
SUMMARY
If you go back now and read this blog and read this one written 20 years apart you will see all the parts but I could not give you all the details because you did not know enough about light, water, and magnetism to understand how POMC fundamentally works with UV light.
This is my Black Swan mitochondriac perspective today. I taught myself to see and now I teach it to the masses who want to learn how we really work. We know BMI is not a universal constant in biology or physics, but we wrongly assume ‘big G’ is such a constant on Earth when we consider gravity. It cannot be a constant because the mass of any body varies with the surface charge given to it via the environment. This means fatness, muscle mass, and body type are a function of the light we live under most. These light waves “sculpt” the colony of bacteria in our gut and the colony of mitochondria in our tissues. This is where variance in humans comes from. It comes from a changing light spectrum. It is never a story about the food macronutrients contrary to what the simple minds tell you and conventional beliefs about dietary guidelines.
Food gurus keep blaming food and never seem to realize how powerful parts of the electromagnetic spectrum are in regulating melanopsin dysfunction in the eye, skin, and gut. Consider this latest warning from a chronobiologic researcher. “It doesn’t matter if you’re male, female, young or old, or what your ethnicity is, your body’s internal clock regulates half your genome,” says new light research data published in @ScienceTM http://bit.ly/2x7kNII#melanopsinwisdom. I wonder when Nina Teicholz and Gary Taubes will begin to study what really matters instead the blaming the dietary guideline for the obesity crisis. You must stop blaming food for what artificial partial light spectrum causes.
Food gurus only report on what makes them famous and rich.
CITES
https://www.cdc.gov/obesity/data/prevalence-maps.html
https://www.science.org/doi/10.1126/scitranslmed.aat8806
Barrera FJ, Yust B, Mimun LC, Nash KL, Tsin AT, Sardar DK. Optical and spectroscopic properties of human whole blood and plasma with and without Y2O3 and Nd3þ:Y2O3 nanoparticles. Lasers Med Sci. 2013;28(6):1559-1566.
Mace K A, Yu D H, Praydar K Z, Boudreau N. Sustained expression of HIF-1α in the diabetic environment promotes angiogenesis and cutaneous wound repair. Wound Rep Reg 2007: 15: 636– 645.
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