DECENTRALIZED MEDICINE #6: WHY ARE THE TROPICS HEALING?

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