Our eutherian cousins that can still hibernate increase their brains' ascorbic acid reserves before entering hibernation. This tells me they are increasing their ability to use magnetochemistry and the radical triad method in quantum mechanics I covered in the Decentralized medicine blogs. This helps water flow in aquaporins in the CNS and PNS using proton tunneling. Hibernation is linked to winter and a lack of environmental UV light, while cold temperatures affect changes in the leptin-melanocortin pathway. This increases endogenous UV light production from metabolism to increase ultraweak UV bio-photons. These actions increase blood glucose from POMC cleavage to act as antifreeze in the plasma. The light a semiconductor interacts with emits different light spectra, which can be used to complete different physiologic tasks in a cell.

Chronic cold exposure is the only thing that shuts down IGF-1 and mTOR simultaneously safely without affecting longevity or telomere biology. Why? Endogenous UV light controls mTOR biology and does not allow for changes in basal metabolic rate during starvation in hibernation. The endogenous UV light stimulates thyroid function, so BMR increases to help burn the animal's fat stores during torpor. Moreover, the cold temperature causes insulin to become impotent and causes disease from insulin resistance because insulin loses its compelling power in cold below 62 F degrees. Insulin works biochemically differently in summer than in winter due to its temperature lability.
And here is the bigger shocker: Glucose is the only thing that can slow down timing the clock genes in front of every somatic mammalian gene. This allows it to control the ROS/RNS function to ensure timing is quantum precise. Getting the effect requires cold, so hibernation is linked to freezing temperatures when UV light is absent.

Contrary to popular belief, The Warburg effect, which uses glucose and glucogenic amino acids, has other roles for us because humans never face a proper winter. We lose the ability to see those effects, but they still operate in us when we get out of nature's way.
Ketosis lacks environmental context, and not all versions of ketosis are equivalent. This is why a ketogenic diet is not always effective.

What is the proof of this: superoxide levels and ubiquitination rates.......and F:N ratios in mitochondria........but no one is looking there; guys like Gary Taubes and Nick Norwitz and his food guru buddies need to back off the ketone measurements and focus on the real prize.......superoxide, ROS, RNS levels use for signaling in different tissues. Each tissue has a different threshold, and this is why ketosis is not a fixed problem for cancer. Food can never fix a quantum-based disease. Cancer is that type of disease.
It turns out that PD, AD, T1D, T2D, and AI all have super low superoxide pulses from their cytochromes because the blue light in those people's environments is destroying circadian clock management in the leptin-melanocortin system. If you can’t make SO, you cannot enter autophagy to recycle redox-shifted mitochondria. And protons outflow from cytochromes is affected. The flow of electrons can reverse as well.

PHOTONIC OVER ELECTRONICS IS AN ANCIENT MEME THAT IS CODIFIED IN THE ART OF THE SPHINX

When this happens, you remain sick, have a lousy body composition, low T, low IGF 1, and become infertile regardless of how much fat you eat. To ……burn fat properly outside of torpor, mammals must see the AM sunrise. If they do not, this stimulates the torpor response. You never see the effect if you are not cold and ground as a mammal should be. And since evolution is about reproduction, if you’re infertile, it means you need to ask better questions to your food gurus. Not one of them will ever put this together for you.
Why don't I see that from food gurus or biochemists? It is terrible for their business models.
Rest assured, there is a decentralized answer, and that answer is in SO and F:N ratios and the variation in voltages in cell membranes induced by light to alter your CO2 and BUN/creatine ratios. These exhaust fumes from metabolism link to the bio-photons spectrum you can create within your colony of mitochondria in a tissue.
You need to go back and really carefully read Warburg's work. Few have. He found a prize about something other than glucose.
These altered distances and movements of mitochondria to the nucleus are critical in developing diseases like cancer. Why? The further the mitochondria move from the nucleus, the more pseudo-hypoxic the nucleus gets. The less O2 the nucleus receives, the less chance ROS and RNS are made. This tells us the Warburg metabolism is about trying to reset the lousy timing inside the cell from the effect of the light environment. The worse the circadian mismatch is, the more it favors a Warburg metabolism to limit ROS damage. Glucose allows for small amounts of ATP, and ATP is made more rapidly than it can be via the TCA cycle. The TCA cycle takes much longer at the quantum level to create ATP inside the cell. ATP allows the unfolding of proteins and provides water to engage the protons and electrons in those semiconductive proteins. In ubiquitination 5, we tackled this mechanism.


Now you can see why I do not believe the Warburg metabolism is terrible. The mammalian retina uses it to limit ROS/RNS because the retina is always photooxidized from light use during the day. Glucose is the emergency break for circadian clock genes that sit right before our somatic genes. nnEMF creates massive ROS/RNS while causing a decrease in CO2 and water production from a cell. 

Today plants that evolved during the last CO2 famine will be the best plants to surround yourself with if you live in a nnEMF shithole. If you love the smell of gardenia, bourgonvilla, and magnolia, it tells me that your colony of mitochondria is not making enough CO2 or water.
Some will look at a plumeria flower (gardenia/magnolia) and try to tell us that its creation results from perfection in minimalism, but this only reveals what they do not know about thermodynamics. It is false. For me, it reflects the melanin sheets in their olfactory grove. People with lighter eyes and pale skin will be more drawn to these scents because of the lack of melanin in their three layer cortex in the olfactory nerve.

The Plumeria flower and the Trevi fountain represent opposite poles of the complexity argument I am explaining to you here. When life was simple, there was little oxygen, and we used glucose metabolism freely. A simple life requires simple biochemistry. Simple life always had a tightly coupled light and dark cycle because they had to exist by the dictates of their environments. Only eukaryotes can break this rule because they can change their environments. Humans are the most significant mismatch that Nature has built because of what their brains became capable of.
Did you know flowering plants like the plumeria species occur due to a lack of CO2 energy? So, their analogy is poor. They are minimalistic flowers/plants because of their low-energy environment. They are great examples of my point.
Plants also are made of DC electric semiconductors like we are. They reflect the light in their environment, structure, and phylogeny. Most plant groups were relatively unscathed by the Permo-Triassic extinction event, although the structures of communities changed. This may have set the scene for the appearance of the flowering plants in the Triassic (~200 million years ago), and their later diversification in the Cretaceous and Paleogene.

The latest major group of plants to evolve were the grasses, which became important in the mid-Paleogene from around 40 million years ago. The grasses, as well as many other groups, evolved new mechanisms of metabolism to survive the low CO2 environments linked to warm, dry conditions of the tropics over the last 10 million years. Beauty varies as environmental energies vary. Note the CO2 levels that PRIMATES EVOLVED. Note today, we are only at 420 parts per million. Modern humans forget that plants need CO2 to grow because of how photosynthesis works.

SUMMARY
Focusing on things out of your control, whether true or not, is a disempowering strategy. Focusing on methods and solutions to reverse a disease is better than treating it with a centralized Rx. This is what a decentrlaized leader advocates. The first responsibility of a decentrlaized healer is to define a reality that is a problem today and offer a durable solution. The last is to say thank you. In between, the leader becomes a servant to the public’s health. I plan to do this in El Salvador’s new healthcare system.
CITES
1. https://www.youtube.com/watch?v=2Xfa_V30tR0
Preston
2024-08-26 02:13:46 +0000 UTCDr. Jack Kruse
2024-08-19 12:22:07 +0000 UTCRoman S Shapoval
2024-08-18 23:10:25 +0000 UTCDr. Jack Kruse
2024-08-17 13:53:18 +0000 UTCDr. Jack Kruse
2024-08-17 12:29:25 +0000 UTCDr. Jack Kruse
2024-08-17 12:29:15 +0000 UTCSimon
2024-08-17 08:22:21 +0000 UTCAnthony Serdar
2024-08-16 20:05:54 +0000 UTCDDH
2024-08-16 14:37:29 +0000 UTC