https://www.youtube.com/watch?v=b7iuFIKmkN4
THEORY OF CONSCIOUSNESS DEVELOPMENT VIA POMC
THE THERMODYNAMIC PROBLEM OF CONSTRUCTION OF THE HUMAN BRAIN FROM VERSION 1.0 FOUND IN CEPHALOPODS:
One of the most amazing things about the human brain is that it is capable of performing trillions of computations during consciousness while using a very low power voltage—on the order of 20 watts. No one knows how this process happens.
If you have any light bulbs in your house, you will see that even your refrigerator light bulb uses more power than your brain, and it can only turn light on and off when the door opens. When you have a basic understanding of how one can engineer a low-power computer with a lot of computer memory, you will then need to know a little bit about Noether’s theorem, mass equivalence equations, and the controlling magnetic domains.
KEY BLOG POINT: At 16:32 in the video above, you discover why melanin and water are the ultimate heat engine. The Carnot theorem is deeply buried in the tissues of all mammals. Mammals absorb light and turn it into heat, rapidly transferred into the water to be buried at the electronic and vibrational level of mammalian cells. Water touches every level of where wide-band gapped semiconductors are. No part of biology is untouched by water. This is why time is a unidirectional arrow in life. Energy flows from hot to cold. This includes light energy from the sun. This defines entropy. So when melanin degenerates, the energy buried in water cannot get more energy buried into it. This means the semiconductors become starved of energy = fibromyalgia, cognitive fog, TBI, PCOS, NAFLD, and obesity. Get it. Melanin renovation solves the entropy story in all mammals.
Most people know that computers use magnetic drives to store memory in digital form. The problem is that magnetic drives are the energy hog in computers, and it has been a real problem in extending the battery life of computers or, for that matter, any technology that uses batteries. So far, in the technology industry, they have tried to better the situation by improving battery technology and using lithium-based batteries, but this is problematic because these batteries cannot be safely shipped via planes all over the world because of their vulnerability to explosions and fire. (Carnot)
I have told you that as part of the three-legged stool, light, water, and magnetism in Energy and Epigenetics 4, all life organizes around these three concepts. In fact, the atomic and molecular organization of the cell is critical in understanding these foundational principles. So, how does the cell maintain “battery power” across all the collagen and water semiconductors in the human body? ATP is the first layer of energy generation but it is not the most important.
There are 2 main processes that determine health, illness, and body composition for humans. You must increase your ability to collect photons or you can increase your magnetic moment by capturing as many photons and electrons as you can in your life. To begin with, the tissues in your body must be put in a position to collect photons and electrons.
This aspect of health is 100% controlled by proper circadian signaling of the environment sensed by the brain. Then, you must be able to assimilate or catch the electrons and photons to stream and move them in semiconductive circuits where they are needed within your internal power grid. The wide band gapped semiconductors I have described to you in this series create stronger light inside of you than the sun provides to your body. This light has to be captured to be made useful. The topologic insulators within you, like melanin, help you accomplish that task. Your brain captures DHA from the marine photosynthetic chain and puts it in the cell membranes of the retinohypothalamic tract before the melanin targets. Cortisol via ACTH from POMC slows the immune response, and the breakdown products of DHA, resolvins, protectins, and maresins stop the inflammatory cascade and begin the recovery and wound healing part of the cascade in the immune system. POMC controls both arms of immunity.
Interestingly, when mitochondrial redox is low, and heteroplasmy rates are high, DHA is not efficiently transformed into resolvins, protectins, and maresins. DHA also lowers SCD1 to push biochemistry from the highly inflammatory omega-6 pathway into the omega-3 pathways, stopping inflammation and beginning wound healing via resolvins, protectins, and maresins created from the omega-3 fats. This is also true in older people who take exogenous DHA. Taking DHA, in that case, has no benefit and may hurt people who have built-in poor redox chemistry at the tissue level because of mtDNA dysfunction that limits the VUV-IR-A at our wide band-gapped semiconductors. DHA also provides a break in inflammation to allow for wound healing.
At life’s genesis chaos has to gain order. Dissipative structure theory really aims to solve this problem for cellular biology. It uses AMO physics to get the job done. Remember that stored energy in cells is coherent energy in water. 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.
This arrangement allows us to capture photons efficiently. In this atomic arrangement, your cell membrane becomes an antenna for the electromagnetic force found locally in your environment.
Like most things in the technology industry, the new technological advances are based upon an expanding knowledge of solid-state quantum physics. The ironic finding is that Lady Evolution has been using this epigenetic tool chest to build us for 4.6 billion years with her quantum blueprint as well. The problem is today, in centralized science, few people know it. The human brain uses many photoelectric switches in proteins to control light & water’s magnetic domains in our tissues. In the human brain, this innovation in neurons and cerebral spinal fluid has had spectacular returns on equity for Nature. Humans also benefit from this arrangement in the extracellular and intracellular spaces because the water flows between neurons and glial cells become controllable by light frequency changes to lower power consumption.
POMC allows the transmission of electromagnetic waves into tissues to create a time-varying media for biology.
POMC translation into tissues changes the crystalline nature of tissues because the chemicals cleaved by POMC create massive amounts of electrons. This allows different frequencies of light to be captured and be made useful physiologically. What are the implications of this ability?
Time reflections in tissues occur when the entire medium in which an electromagnetic wave travels suddenly changes course. This causes a portion of that wave to reverse, and its frequency transforms into another one. This means that we will see different flickering colors within a material. It also implies that tissue has to be littered with many different proteins that are able to respond to the creation of different colors.
- For more than 50 years, scientists theorized that an electromagnetic wave could be reflected temporally—not just spatially.
- Scientists have been unable to confirm the existence of time reflection due to the amount of energy required to create a temporal interface.
- Understanding Noether’s theorem helps make sense of this phenomenon in biology.
The explanation of spatial reflections—whether by light or by sound—is pretty intuitive. Electromagnetic radiation in the form of light or sound waves hits a mirror or wall respectively and changes course. This allows our eyes to see a reflection or echo of the original input. However, for more than 50 years (since 1971), scientists have theorized that there’s another kind of reflection in quantum mechanics known as “time reflection.”
Energy is understood well in physics because of Einstein’s mass equivalence equation and Noether’s theorem. Energy is a physical concept but is not really explained well in biology. We know what E=mc^2 means, but what does her theorem tell us?
Emily Noether taught us that with respect to energy and momentum in the universe, light energy “informs” space and time how to curve. Space and time inside of a cell link to Fermat’s equations of how light travels in a medium. Fermat’s principle states that “light travels between two points along the path that requires the least time, as compared to other nearby paths.”
From Fermat’s principle, one can derive
(a) the law of reflection [the angle of incidence is equal to the angle of reflection]
(b) the law of refraction [Snell’s law].
I discussed this recently in a podcast with Sarah Pugh, Ph.D. of the UK.
Noether’s equation says that any symmetry, either local or global, implies there must be a conservation of some physical quality in reference to energy transformation to keep the system functioning. Mammals break TIME symmetry by conserving and amplifying POMC biology in their tissues. The POMC is translated the more light and charge can be stored at the vibrational and electronic level. POMC is only translated by “specific frequencies of light in the UV range but cleavage decisions are made by other frequencies of light. Most people have no idea that just about everything I post about POMC/melanin falls directly in line with Noether’s idea in biology. They will soon.
The big question right now should be in your head why have scientists worked toward recreating this theoretical time reflection in a laboratory experiment? This process allows more minute control of electromagnetic waves and it can vastly improve wireless communications which would lead to advancements in low-energy, wave-based computers.
Nature did this long ago with cephalopods 10 million years after the Cambrian explosion and this process was refined by the evolution of the nervous system all the way into the mammalian clade. Humans today have the latest refinement of this process in the skulls and it was driven by POMC biology and wide-band gapped semiconductors that could take visible light and use it to change it to light frequencies more powerful in our interiors via the innovation of light chromophore proteins (melanopsin, flavins, B12, B3, NAD+, Vitamin A, Vitamin D, etc..) so that this light could be captured by our melanin sheets deep inside our tissues for physiologic use. This process explains how the human brain only needs 20 watts to operate.
In other words, Noether’s theorem allows us to know everything there is about electromagnetic waves—both forward and backward. When melanin is renovated, the right side of the top level of the slide below allows cells to go right to left and REGENERATE thermodynamically.
We can regenerate melanoma, PD, or anything else tied to it because of the ideas in this blog and the video above. When you hear the podcast I did with Sara Pugh, Ph.D., be ready for shock waves.
At 54:30 from the video above. Melanin is “the tokamak” of the quantum cell. Quantum engineering of Nature was perfected in mammals.
ENERGY IS BURIED AT THE ELECTRONIC LEVEL IN CELLS
The energy derived from the sun is stored coherently in cells and ready for use over all space-time domains. Sunlight is transformed by semiconductive proteins into electrical signals. Mitochondrial water production is critical in the blueprint. How cells transform solar energy is 100% based upon QFT/QED and not the classic biological dogma all physicians and scientists learned in their training. These semiconductive proteins in our cells have side groups that have special molecular abilities. The primary and secondary protein structures are determined by the DNA code. This relationship maintains the selection of proteins that are capable of a specific type of semiconduction (hydrated wide band gapped) essentially dictates how cell water can or can not bind to the backbone of the protein to work. The instructions for this blueprint are built directly into the DNA and RNA code. No other energy is needed to maintain this organization. This binding has huge implications on how biochemistry can or can not act within a cell. Tertiary and quaternary protein bending is required for final tissue-level physiology. This protein bending requires accurate timing by using incoming solar energy to the organism via the eye and skin. This is where POMC becomes very important in mammals. Deciphering signals in light can happen at night time because light energy is stored in the cell’s protoplasm when the sun is not present. Melatonin is a great example of this. An inability to transform energy is why bent proteins seem to be found in cells that have poor optical control and show up in many neolithic diseases today.
Consider ATP as an example.
ATP is a natural electron-withdrawing protein, so its “real purpose” in a cell, organized in a quantized fashion, is to strip electrons to make proteins more positively charged. The waste product of ATP is adenosine and this is a signal that tells the brainstem it is time to sleep. When a protein gains electrons, it becomes reduced, and its charge changes, and when it loses them, it becomes more oxidized, and its charge density changes as well. Since proteins can both gain and lose electrons in this way, they can vary their charges between these electronic states, making them very reactive to low electromagnetic forces. This confirms the ideas of Albert Szent Gyorgi in 1941.
He predicted in 1941 that proteins are capable of semiconducting electrons when you look at their atomic molecular arrangements. He had no idea how protein bends, water, and atomic arrangement around the protein bends could be changed to control the actions of chemicals in biochemical pathways. He won a Nobel Prize. This molecular arrangement in cells allows for the creation of low-powered currents to gain directionality in tissues. This directionality links to the flow of entropy laid out by Carnot’s theorem above. Becker found when you renovated melanin with the DC electric current in animals, regeneration was possible. Becker found this in his regeneration experiments in the CNS and PNS on salamanders, frogs, and humans. This alteration of charge density is a critical point to understand because the charge is a conserved quantum mechanically.
What about some other biomolecules?
MELANIN + DHA + NAD+ + sunlight + heteroplasmy rate = optimize Kleiber’s slope line for humans. Anyone who tells you that Artificial Intelligence or any supplement/drug will substantially increase longevity does not understand the thermodynamics of life. Water is the key to Kleiber’s law because melanin dumps its entropy into water for further physiological use. The intrinsic value of vitamin B3- which is derived from NAD+ of cytochrome one leads to atrophic skin. When you use exogenous NAD+, it leads humans to a hyper-photosensitivity to sunlight. This is why so many are solar-sensitive or are told they are “allergic” to the sun. The reality is that they are deficient in NAD+ & have horrendous redox. NAD+ captures electrons and protons for mitochondria. This lady below was using NAD+ analogs to cause her skin changes.
SUMMARY
It turns out that photons and magnetic fields have innate solid-state effects which depend less on the energy of the field within the environment than on the ability of the field to orient molecules and atoms with light and magnetic moments. This sets the stage to develop quantum coherence in tissues and the development of the conscious state in life. As such, this gives them the possibility, based upon their ability to deflect moving charges. This ability is directly proportional to how well the 3-dimensional arrangement of the molecule, with the magnetic domain, can break symmetry in the system. Water is the ideal symmetry breaker in biology. The asymmetry of the water molecule is due to the 105-degree bond angle between the two hydrogens in relation to oxygen. This arrangement leads to a dipole moment in the symmetry plane pointed toward the more positive hydrogen atoms. In physics, however, symmetry means uniformity or invariance, or “the existence of different viewpoints from which the system appears the same” (Anderson 1972). Symmetry breaking is the process by which such uniformity is broken, or the number of points to view invariance is reduced to generate a more structured and improbable state. This new state requires that energy be transferred. What emerges from a break in symmetry is a new emergent property of matter. Water changes things. It is a molecular adapter that transfers energy to different forums for use.
It turns out water has this built-in ability because it is a perfect molecular magnetic dipole. It is asymmetric because of its binding angles. This is why just about everything can be dissolved in water. Water has the ability to transform into many forms itself, and it can transform many other sources of matter into something else quite easily. We use water’s asymmetry to break electrons from oxygen everywhere in our body. This means water is the perfect molecule to break symmetry in any thermodynamic problem. This should be no surprise to anyone with a basic chemistry background. Life & longevity are fundamentally thermodynamic problems.
Most people are not interested in learning what truth is. They would sooner sit in front of a box that continuously spits out lies and misinformation and entertains them. Why are we addicted to distraction in this modern world? Is it our weakness, or is it done to us by design? Is it possible that all profound distractions open certain doors in our imagination? Do we have to allow ourselves to be distracted when we cannot concentrate or focus on the reality of what is happening around us? Might it be that our dreaming imagination self seeks to tell us something your waking ears refuse to hear or accept?
Right now, longevity perspectives are dominated by mTOR biology.
Why is mTOR biology operational from yeast to mammals but not human mammals? The answer is in the way humans use POMC biophysically. Sabatini has no idea how glucose, oxygen, and phosphorous operate upstream of human mTOR, but he admits it publically when he speaks and I respect that. My podcast with Rubin and Huberman answers it. Wide-band gapped semiconductors make the light that controls the entire pathway rostral to Sabatini’s discoveries 28 years ago from Easter Island.
380 nm light is the switch between catabolism and anabolism in the mTOR pathway. Living below 380 nm light is where longevity happens in human mammals because of the translation of the POMC gene. That is where Noether’s theorem comes into the story. The mTOR biology links directly to the mammalian POMC story. How?
Neuropsin (OPN5) is an opsin family member known to function as a photopigment responsive to wavelengths in the near-UV (λmax = 380 nm). Now you know why mammals have the non-visual photoreceptor neuropsin in their most important tissues in the cornea, skin, and brain. OPN5 informs the mTOR complex how to act physiologically in a tissue. Should it be anabolic or catabolic? When Sabatini understands how light controls the mTOR complex, then and only then should he get his Nobel Prize.
CITES