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Dr. Jack Kruse
Dr. Jack Kruse

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QUANTUM ENGINEERING #72: MELANIN SUPERPOSITION

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 in mtDNA.

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 as they aged in their own lives with their light choices.

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/

QUANTUM ENGINEERING #72:  MELANIN SUPERPOSITION QUANTUM ENGINEERING #72:  MELANIN SUPERPOSITION

Comments

Curious your thoughts on methylene blue, Jack. Have you published any literature regarding it? I have found it to help my eyes a ton, in tandem with morning sunlight exposure. Now I’m seeing that in may influence the NAD+/NADH ratio, which should be regulated solely through sunlight. Is it beneficial to dose in the absence of light and will it impact by morning activities if I do it this way? Thanks ! Happy to be part of your community.

Lance Mezh

Beautifully written again Jack🙏

Stian Van Zweden

Do I ? Yes. It is another timing disease due to bad light choices.

Dr. Jack Kruse

Do you believe in adhd? My dad and brother have it. they spend a lot of time with technology and social media. I tell them that they could build up there attention span by starting with 1 minute and gradual going up to a few hours. My thinking is if they don't use it they lost it. They definitely need more sun as well.

chad brown

Discussion can only happen if you are member of the website not just patreon. info@kruseatdestin.

Dr. Jack Kruse

yes they do

Dr. Jack Kruse

New to the community. Started morning sunwalks 9 days ago, orange blue-blocking lenses while on the computer all day, will remember to ground - feel much better and lost 0.8 pounds per day without any attempt. Jack mentioned in a writing or podcast that people with retinal damage low in the eye (computer screen blue light) tend to have symptoms of hypothyroid, obesity, diabetes, high blood pressure, peripheral arterial issues, muscle weakness, out of breath. The hypothyroid has not been diagnosed, but 3 mg of iodine/salt once a week mostly fixes the extreme muscle weakness. Because you were speaking directly to me, I got started. I need to learn about the cold therapy protocol (38 North). I planned on testing this protocol for a year to see if there was improvement. It took a day or two (I was not paying attention). The dyspnea (out of breath) is 90% better especially considering my considerable weight, sugar response to insulin much better by 200 mg/dl, I feel much better in general, systolic blood pressure is down 20, and 8 pounds weight loss. Thank you! My concern was that my eyes were too damaged for the POMC system to work. It seems the POMC pathways are working, at least enough, based on the rapid results. This is health and life saving!

M Inmyopn

Quantum dots QDs are great probes in theory. Experiments in cell culture might be relevant when QDs are used. Maybe someone with experience with QD probes in cultured cells could comment. In animal experiments, QDs have a level of toxicity that increases with each dose when administered periodically. This might be similar to the immune response referred to as the Shwartzman Reaction. Endotoxic shock is an example of a Shwartzman Reaction. https://pubmed.ncbi.nlm.nih.gov/36764372/ Question: do QDs perturb studies in cell cultures? This QD topic is more for my knowledge and does not contradict the points made about how our cells obtain or create specific energy and deal with wastes.

M Inmyopn

very much enjoyed the content of this post as well as the bonus material in the comments. thank you.

James Paulus

Jack- Fellow MD here- I’m an integrative medicine doc that focuses on Dermatology and fully embrace your ‘inconvenient’ paradigm. My best friend (brother from another mother)’s father (his hero) has brain melanoma mets and I think there’s maybe the opportunity to help here. The man was a first responder to 9/11. Was chief of NYPD in early 2000’s. He’s saved many lives. They suspect melanoma is due to exposure at 9/11 event. I would love to discuss with you if you’d be willing. -Fellow MD trying to make sense of the nonsense we call medicine. - George

George Gavrila

Hi Jack, your a master of quantum biology, and how you explain its relevance and predictability in our unhealthy anthropogenic world of nnEmf confusion and delusion. This post is exceptional, and again very carefully crafted into a symphony of facts, references and cohesion. Your investigations into quantum nature of large biomolecules, resonant frequency and function is illuminating for me..THANKYOU. As a retired engineer, with majors in physics, chemistry, thermodynamics, and understanding of crystals, spectrophotometry, and xray diffraction in solids everything you post makes perfect sense. When my sick friends and GP ask me how I have recovered from chronic fatigue, fibromyalgia and prostrate cancer I'm always referring to your skillfull and innate ability to explain things, making them become Mitochondriacs and question, to really think ...deeply and critically about their health advice, guiding towards your work, and helping them to understand your insights. As such, I am more familar with atomic and chemical spectral emissions, field electrical, magnetic forces. With your posts, I now connect with vibrational energies of harmonics and molecular cohesion with native Emf have applied these to reset myself, and friends suffering chronic illneses. Always, following your insight of seasonal and diurnal sunlight Emf its spectra, and magical power of water molecules, and cell ATP, biological utility of electrical magnetism within us and its power to move quantum things. I try to open their minds and field of view to the natural world you positively connect with in your posts..BTW, I used your posts and Suns noon day UV spectrum to improve recovery from two bouts of COVID 19 infections over the past 2-3yrs. Your a wonderful teacher Jack... thankyou, again. I believe future investions into quantum biology of cells will find our biophysical abilities may be faster than speed of light experiments (deduced for a vacuum)..particularly for a healthy CNS, and speed of information Emf travel across a brain cell synapse. Or, maybe how light frequencies move cohesively and resonantly within our brain-body in a symphony with its magnetic fields and our environment..I would liken this metaphor to perhaps, how the electric universe theory and plasma physics explains-predicts the workings of the cosmos, and how Birkland currents connect all things we understand for astronomy and in particular the Earth's electromagnetic connection and communication to the Sun.. perhaps, our homosapien brains are connected to these cosmic fields as well... by some philosophers we are all connected with "a universal intelligence". It's a happy thought of quantum duality, and superposition too. All the best from Oz, Down Under.

Chris Sussmilch

https://x.com/DrJackKruse/status/1763942470641983863

Dr. Jack Kruse

What got me home? Hypocretin and melanin-concentrating hormone (MCH) are expressed by different cell populations in the Lateral Hypothalamus. I learned this in residency. (Broberger et al., 1998; Elias et al., 1998; Peyron et al., 1998). The hypocretin system enhances arousal (Hagan et al., 1999), potentially related to metabolic state (Yamanaka et al., 2003), and loss of hypocretin peptide or its receptors results in narcolepsy (Chemelli et al., 1999; Lin et al., 1999; Nishino et al., 2000; Peyron et al., 2000; Thannickal et al., 2000). MCH neurons were also be involved in the regulation of energy homeostasis but in a rather counterintuitive way. MCH injections into the brain cause a robust increase in food intake (Qu et al., 1996; Rossi et al., 1999); blockade of the MCH receptor reduces body weight (Borowsky et al., 2002). When melanin was stimulated via POMC it always controls appetite and food intake. Because of the relationship of MCH and melanin it told me light had to be the trigger I was missing. This is when I thought back to the lesson of Julian Battle from the Monk book going to the top of mountain coming back tan, fit, and less of an asshole. It all clicked in a moment.

Dr. Jack Kruse

Glucagon-like peptide 1 (GLP-1) is synthesized in the brain (Han et al., 1986; Jin et al., 1988; Larsen et al., 1997a), in which it may act as a neuromodulator (Kreymann et al., 1989). GLP-1 has been detected in the caudal brainstem in a subset of neurons in the nucleus of the solitary tract (NTS), a key relay of interoceptive information from the gut linked to the vagus nerve in humans (Larsen et al., 1997a; Merchenthaler et al., 1999; Saper, 2002). GLP-1-containing axons ramify widely throughout the hypothalamus, particularly in the paraventricular nucleus (PVN), arcuate, and lateral hypothalamic (LH) regions (Han et al., 1986; Jin et al., 1988; Rinaman, 1999). These were the early neurosurgery links that would eventually form the Leptin Rx.

Dr. Jack Kruse

GLP-1 axons and receptors are heavily populated in the lateral hypothalamus, where hypocretin neurons are found. I knew this in 1999. I also realized after I read the Monk who Sold his Ferrari that this area was likely where sunrises where changing us via the electromagnetic force to control physiological actions of foods via the GLP-1 system. That is why I wrote a blog on narcolepsy 15 years ago. Paraventricular hypothalamic neurons were also directly excited by GLP-1 agonists. In contrast, GLP-1 agonists had no detectable effect on neurons that synthesize melanin-concentrating hormone (MCH). This clued me in that melanin was a huge part of this story.

Dr. Jack Kruse

This is remarkable! Thank you Dr. Kruse for organizing this impactful data. I believe you’re impacting a lot of lives by conveying this knowledge. I personally- can not thank you enough. You’re the man Jack!

George Gavrila

Insulin is another solar hormone I've written about – which is produced by a gut organ called the pancreas – acts like a key to unlock the cells’ ability to absorb glucose from the bloodstream through the cell wall. The glucose that is absorbed is then used as energy by mitochondria. It is the eye, mouth, tongue, skin, and pancreas that all need to be working in unison with sunlight to sense the right amount of the hormone insulin needed to be released for this whole process to function properly. With diabetes, this sensation process is faulty for many reasons. Most are related to light defects. There are two types of diabetes. Type 1 diabetes is a condition in which the pancreas produces little or no insulin, and it usually starts early in life. In Type 2 diabetes – which accounts for 95% of diabetes cases – cells stop recognizing and responding to insulin, and this is referred to as insulin resistance. With insulin resistance, glucose levels in the body rise after we have eaten, the pancreas detects the rising levels of glucose and produces more insulin to reduce glucose levels. When glucose levels continue building in the blood, this is referred to as glucose intolerance. Because of this there aDEEP link between Parkinson’s and diabetes tied to LIGHT. For a long time researchers have known that there is a close relationship between Parkinson’s and diabetes; a significant proportion of people with Parkinson’s have glucose intolerance and some also live with the added burden of diabetes. Insulin also does its job of controlling glucose levels in the brain. Insulin has been shown to impact dopamine levels – dopamine is a chemical released in the brain and used to send messages between nerve cells. This blog lays out some of those details. Research shows that insulin also helps with our cognitive function – the ability to think clearly, to learn, and remember. Notably, defects in insulin processes in the brain may contribute to Parkinson’s and the dementia associated with it.

Dr. Jack Kruse

Glucagon-like peptide 1 receptor agonists, or GLP-1R agonists, are a class of drugs that function by mimicking the action of naturally produced hormones in the gut called ‘incretins’. Hypocretin was the term used in the literature when I wrote about them 20 years ago. These gut hormones work by helping the body produce insulin when needed, they also reduce the amount of glucose released from where it is stored in the liver, they reduce the rate that the stomach digests food and empties, and can also reduce appetite. When eating food, the gut hormones stimulate the pancreas to release insulin needed to help cells absorb the glucose from our food. Receptors responding to these incretin gut hormones are present throughout the body including the brain. GLP-1 Receptor agonists act by increasing the action of the incretins or gut hormones in the body. Many studies have shown that GLP-1R agonists actions in the brain occur in a variety of ways; effecting neurogenesis (the process by which new neurons are formed in the brain), improving energy function, and providing a supportive and protective effect. The first GLP-1R agonist approved for the treatment of diabetes was exenatide. I think some of these drugs maybe used in autism research because of their neurogenesis effects.

Dr. Jack Kruse

Drugs aren’t the only way to stimulate hunger-controlling parts of the brain — electricity can work, too. Functional neurosurgeons implant wires into brains where melanin is missing. In November 2022, researchers at Penn announced that stimulating a part of the brain called the “nucleus accumbens” aided weight loss in two severely obese women with binge eating disorder (BED), a disorder characterized by episodes of rapidly eating a lot of food while feeling a loss of control. While BED itself isn’t as common as obesity, 70% of people with the disorder are obese, and the study demonstrates how identifying and stimulating the right parts of the brain can help people limit their food intake. In terms of treating obesity, a team from Allegheny Health Network thinks it might know what the “right” part is, too. In 2021, they launched a small trial to stimulate an area called the “lateral hypothalamus” in the hope it will help regulate hunger in people with obesity. Those results are expected in 2025. While both the AHN and Penn treatments require patients to undergo invasive electrode implantation surgeries with neurosurgeons, researchers are developing less-invasive methods for stimulating regions in the brain using GLP-1 drugs. Now you can see why my TED talk was so problematic for BigHarma. They have billions on the line keeping people out of the sun and using sunscreen contacts and sunglasses.

Dr. Jack Kruse

These lifestyle drugs are getting ready to get another large boost soon. Novo Nordisk has announced via its financial reporting requirements that preliminary results from a trial that has been running since 2017, which found that semaglutide reduced the risk of heart attacks, strokes, or death from heart disease by 20%. If confirmed, this major payoff to overall health could encourage more insurers and Medicare to cover the drug and, potentially, other weight loss prescriptions. They are studying PD in this trial. I know it will help PD because these drugs mimic AM sunlight effects as I wrote about in the Leptin Rx. Most people know that neurosurgeons implant DBS into the Globus pallidus for PD treatment. This effectively adds a DC electrode to this pat of the brain to keep endogenous dopamine and melanin operational. The sun normally provides a DC elctric current via your eyes and skin. When this is defective, PD symptoms can manifest. This isn't the only disorder these drugs are being studied in neurosurgery.

Dr. Jack Kruse

The 3 GLP-1 drugs approved for weight loss are Novo Nordisk’s Wegovy (semaglutide) and Saxenda (liraglutide) — Eli Lilly’s drug Mounjaro (tirzepatide) has been added to the group and will now be heavily pushed in Europe. If you understand this blog well, you'll likely figure out that the GLP-1 drugs can help people with PD because of their defective mitochondria and higher than normal blood glucose. Red light will reduce the BG, and if you add UV it will go down even further. But most people with PD are like MS patients. They live far from the equator and they are within 75 miles of large cities. That is why PD has exploded in these areas.

Dr. Jack Kruse

More than 8.5 million people worldwide are living with Parkinson’s, a progressive neurodegenerative disease caused by the loss of brain cells that produce dopamine. This blog links why PD patients have a huge problem with blood glucose. Blue light and nnEMF destroy melanin and this drives blood glucose higher. At the same time these people also are deficient in sunlight with UV and IR-A light. Centralized researchers remain stumped why there is a link between Parkinson’s and diabetes — people with diabetes are 40% more likely to develop Parkinson’s disease and that their symptoms tend to progress more rapidly than in non-diabetics. If you have read this entire series you will remember I mentioned early on about the orexin system and its link to the melanocortin pathways. Hypocretin (Orexin) System is a key stimulus for AM wakefulness followed by the drive to eat. AM sunlight is its most potent stimulus. In the Daniel Prince podcast I did I mentioned this was why my Leptin Rx TED talk was removed. The GLP-1 drugs mimic AM sunrise. The function of this neuropeptide is thought to promote wakefulness and stimulate appetite. The cell bodies containing hypocretin are located in the dorsolateral hypothalamus and project to the locus coeruleus and numerous other areas of the brain including the cortex. The human GLP-1 hormone, is produced after you eat and acts on the brain in a way that suppresses hunger. GLP-1 agonists were originally developed to treat diabetes in the mid 2000's — and they also lower blood sugar — but doctors noticed that patients placed on them were also losing a lot of weight, leading to studies of the meds as obesity treatments. This all happened when my Leptin Rx was very popular.

Dr. Jack Kruse


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