There is a nanomotor in your mitochondria thats spins 9k rpms, thats faster than a corvet

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Rhonda in a yellow top!!!


Cold shock and heat shock protiens for longevity.
 

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Stephanie sennef with mercola discuss glysophates, deuterium depleted water, structured water, covid911. How they all are connected!!!!!

Sennef has a new book out in june 2021!!!!
 

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In remembrance of American Martyr, Ashli Babbit.
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WHY ARE MITOCHONDRIA HUNGRY FOR CALCIUM IN STRESS?
  • Published on March 10, 2016
Author’s photoJack KruseCEO of Kruse Longevity Center of Florida
Melatonin is a biogenic amine made by the interaction of UV light and tryptophan. In vertebrates, like humans, melatonin secretion is regulated by norepinephrine another catecholamine called noradrenaline (synonymous with norepinephrine). It is the main neurotransmitter of the sympathetic nervous system. This system is driven by the PVN in the hypothalamus. It is responsible for tonic and reflexive changes in cardiovascular tone. Here again, we see how a nucleus in the brain stem is linked to the retina where light interacts with the circulatory system where the photo-proteins in RBCs are, porphyrins and hemoglobin. WBC's in humans make huge amounts of melatonin in the blood.
These connections are important for the collection of light frequencies from the surface skin where the circulatory system can reach the surface when incident light hits it. Here you can see how melatonin in the eye, WBC’s, and skin are coupled to the circulatory system. Norepinephrine is a cold-mediated catecholamine hormone. It needs Vitamin C as a co-factor to be made. The same thing is true with cortisol and dopamine.
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Cooling skin temperature stimulates plasma norepinephrine release and allows us to absorb more UV light. UV light also stimulates norepinephrine release when the sun hits our skin and blood plasma. When noradrenaline is released, calcium is released into the cytosol in a quantized fashion to the proportion of UV light assimilated by the cell. The cytosol of a cell is where our mitochondria are located.
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This process also controls the flow of magnesium from the cytosol to the matrix via MRS2 transporter. Mitochondria are battery-pack organelles, or cell units with specific functions, that fuel the energy of almost every living cell, and they have an insatiable appetite for calcium. This dehydrates the cells and because magnesium is water-loving, mitochondria get a relative depletion of magnesium. This depletion cannot be repaired with a supplement. We have to lower the heteroplasmy rate so mitochondria can make water as a by-product of glucose metabolism or beta-oxidation of fats like the picture below shows.
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It appears UV light assimilation on our skin limits calcium flow into a mitochondrion deep in our tissues. No one appears to know why fundamentally a lack of UV light increases calcium flows, but I have a sense it is used as a signaling molecule and one that might be involved with inverse beta decay reactions in the matrix. It appears that blue light and nnEMF also stimulate calcium flows into the matrix to destroy the inner mitochondrial membranes delta psi. Right now, it is clear when calcium enters the matrix, ELF- UV light and IR light are liberated from the matrix while the voltage on the inner mitochondrial membrane falls. As this occurs the mitochondrial size expands and the distance between respiratory proteins increases. MICU1 is essential for calcium uptake in mitochondria to control its effects in the matrix. MICU1 however, doesn't span the entire membrane. It needs another protein to do that. MCU, short for β€œmitochondrial calcium uniporter" is its partner protein.

Calcium is toxic to mitochondrial size and the inner mitochondrial geometry when UV light is not exciting electrons, and this is why all cancers seem to be associated with an insatiable appetite for calcium. This calcium release increases the amount of ELF-UV light from fluorophore proteins and respiratory proteins (NADH). In cells under stress, they begin to use the IP3/DAG signaling pathways when mitochondrial proteins are expanded on the inner mitochondrial membrane. This raises calcium and lowers magnesium egress into the matrix while many fluids rush into the matrix to destroy its ability to make electrical energy from chemical substrates.
ELF-UV exposure of the skin and cooling both increase catecholamines and this, in turn, helps increases melatonin secretion in WBC’s to modulate inflammation in the skin and blood plasma. This is why a Warburg metabolism is signaled because all the aromatic amino acids make biogenic amines with UV light due to the photon traps they contain in their benzene rings.
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The aromatic amino acids' interaction with ELF-UV light is what makes things like the biogenic amines from ELF-UV. Every biogenic amine is made this way.......and in a cancer state, there are no biogenic amines being made in high enough quantities. This is why aromatic amino acids are up-regulated with calcium and magnesium drops like a rock in a Warburg metabolism.
In stressed cells, cancer cells, and most illness states there are always abnormal hormone panels. Why? What controls pituitary hormone release? Dopamine and prolactin. Both of them are biogenic amines as well. Solar light builds our hormone panels by building dopamine in our eye, retina, and frontal lobes using aromatic amino acids that absorb UV light. That light is used to power up electrons before they fall back to the ground state.
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The excited electrons can then be properly assigned by acquiring an electron spin in mitochondria at cytochrome 1, where NADH contains massive stores of UV light energy in its proteins. NADH is a fluorophore protein (340nm). In this way, UV light from the sun via our eye acts as the currency in the protein backbones of our compound pharmacy that contains our hormones in our pituitary gland every day to make things we need from solar light.
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When a Warburg metabolism is engaged, a cell is maximally stressed, and the cell is trying to create things it needs to retain the light it has absorbed from its surfaces. We’ve known for decades now that neurons in the brains of people suffering from the neurodegenerative disease are often marked by mitochondrial calcium overload and a falling magnesium level. We still have no idea why it really happens if you read the literature. I think I do have an idea of why it happens because of something I learn about photons.
Large electric and magnetic fields are capable of confine light. This happens in the sun. It also happens that mitochondria make both electric and magnetic fields too. In this way the matrix mimics the physics of the sun. It also turns out that lowered electric and magnetic fields allow for excessive light release. This is used in the sun and it appears this is how mitochondria release ELF-UV biophotons for signaling.
The flow of electrons is tied to the voltage of the mitochondrial membrane. This explains why ketosis is a great tool in any disease with stressed cells and colonies of mitochondria. If you're really interested in understanding the physical mechanisms of the Warburg metabolism, you must know that the electric and magnetic charge on eukaryotic cell membranes by itself, can contain light by QED principles. Modern medicine's problem is that no one in biology realizes this bio-physical fact. And that is why biology struggles with explaining the physical basis of the Warburg metabolism. Ketosis helps this situation but cannot reverse the disease because the power plant remains defective. The matrix has to be replaced and melatonin controls the two change programs in mitochondrial biology.
This is why ketosis helps in many diseases, especially neurodegeneration, seizures, and traumatic brain injury. Ketosis increases the voltages because it increases the sheer number of electrons from fats to boost the electric charge. This boost in voltage improves the tunneling of electrons on the respiratory proteins of ECT. But this increased flow of electrons does nothing to lower heteroplasmy, to decrease the size and shape of mitochondria, and that is the key physical ability that must be restored to reverse an illness. Ketosis is ONLY a tool, not a panacea.
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If the electrons from a ketogenic diet are imprinted with light information in the UV range to become excited, then the situation is improved and melatonin is made to get rid of the poorly functioning mitochondria. Excited UV electrons increase NAD+ at cytochrome one (pic above) while also increasing oxygen delivery to the distal end of ECT since oxygen is the terminal electron acceptor. These things act to help shrink the respiratory protein shrinking and condensing the cristae, while endogenous melatonin production rises.
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I teach my patients and my members how to do that first before I employ nutritional ketosis. A ketogenic diet comes second because the size of your mitochondria is linked to your zip code. Your zip code is linked to the light you live under. Where you live dictates your quantum yield of sunlight. That is what excites our ketogenic food electrons. Those excited electrons are what make free radicals at cytochrome 1. Free radicals have unpaired valence electrons that have either a spin up or spin down. The two spins states mimic the binary system in computing making them the ultimo quantum dots for the quantum computers in your cells called mitochondria. The sun makes very specific free radicals.
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Blue light and nnEMF make deadly free radicals via the Fenton reaction and peroxynitrite pathway.
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We also know that the secretion of many hormones, like insulin, is triggered by calcium spikes in the cell’s cytoplasm. This clearly makes the case that insulin really is a solar hormone. Insulin is anabolic when it is created and released under the power of terrestrial sunlight stimulus and makes things when it is married to UV light from sunlight. This situation varies when you live under ALAN = artificial light at night/day.
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When insulin is released, and no UV light is present simultaneously to excite the electrons from ketosis, we wind up with a Warburg metabolism. Non-native EMF and blue light exposure at night both cause massive increases in calcium flow to the cytosol. This also favors a Warburg metabolism and cells begin to lose ELF-UV. By clearing cytosolic calcium and raising magnesium, mitochondria can shape these photonic signals to control the light it releases. Scientists studying the nexus of energy metabolism and cellular signaling will be particularly interested in MICU1 and MCU and how circadian biology controls these mitochondrial dynamics. A Warburg metabolism is a light-mediated issue, not a food story. Nutritional ketosis cannot solve a quantum problem tied to ALAN or nnEMF.
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Melatonin is a free radical scavenger and it is acting to alkalize the blood plasma in the circulatory system to affect the size of the exclusion zone in the water in blood plasma as well as the lowering the lipoprotein particle size and phenotype in the plasma. This is why altered lipid panels are found in cancer states. The lower melatonin is in WBC’s, the lower the EZ is in blood, and the higher triglycerides are in the blood and one would expect higher levels of inflammation in the blood markers. This is why HS-CRP, ferritin, low Vitamin D3 levels, and lowered sulfated cholesterol are all linked in inflammatory states where stressed cells are absorbing massive amounts of calcium into their mitochondria, which dramatically lowers magnesium in the matrix lowering delta psi, and this causes lower electric and magnetic fields in our colony of mitochondria and as a result, they leak too much ELF-UV which ruins cell signaling. All of these things are associated with the physical decoupling of processes with light and water. This ruins the bio-physics that control the size and shape of the respiratory proteins to lead to disease by raising heteroplasmy rates.
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Our quantum yield or the light we choose to live under is REALLY what determines our light zip code and our disease footprint in the modern world. Our light zip code is more important than our nuclear genetic code when you understand how mitochondria are operating in our cells. This is no joke. It is the basis of 40 years of mitochondrial research by people like Doug Wallace, Nick Lane, Jodi Nunnari, Vamsi Mootha. People laughed at me 3 years ago when I said this publicly .........they won't much longer when they finally read the data from these researchers. Follow the data not the meme of modern genetics. Genes are not the dictator of the genome they respond to it using the senses built into our respiratory proteins. It is clear that mitochondrial mutations appear way before any nuclear changes occur in all diseases including cancer.
Common sense no longer grows in everyone's garden because no sun = no dopamine or melatonin = poor thinking = worse insight = no understanding of evolutionary physics built into mitochondria.
This is why cancer therapy's that have been directed at the nuclear genome since 1971 have failed miserably. You'll never find the buried treasure if you're looking under the wrong stone. Stop looking under stones and begin to look under rainbows. Light, not food, and certainly not the nuclear genome is where the problems lie.
 

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5G. Is messing with your water!!!!

Water is the means, medium & message of life
Article
Full-text available
Mar 2014
Mae-Wan Ho
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Context 1
... hydrogen ion (protons) and electrons go to reduce (fi x) carbon dioxide into carbohydrates and the biomass of photosynthetic organisms, which serve as food for herbivores, and down the food web to include the vast majority of air-breathers. During respiration, carbohydrates are broken down by oxidation (with oxygen) in mitochondria to release energy for growth and reproduction, regener- ating carbon dioxide and water [ 10]. This completes the living dynamo of photosynthesis and respiration, the magic roundabout that turns inanimate substances into living organisms (Fig. 4). However, it takes 12.6 eV to split water, an energetic photon in the soft X-ray region that would destroy life, and is not what green plants and cyanobacteria use. They use mainly red and to some extent blue light in the visible spectrum. More than 50 years ago, Nobel Laureate biochemist Albert Szent-GyΓΆrgyi already suggested [30] that water at interfaces was the key to life. He proposed that water at interfaces such as membranes is in the excited state, which requires considerably less energy to split than water in the ground state. Most if not all water in living organisms is interfacial water, as it is almost never further away from surfaces such as membranes or macromolecules than a fraction of a micron. This is the β€˜liquid crystalline water’ mentioned at the beginning of this article, which is present in all organisms, animals and plants. And chloroplasts where water is split are particularly rich in membrane surfaces, as are mitochondria, where water is regenerated. A sign that interfacial water is excited is a voltage difference at the boundary between interfacial water and bulk water, as predicted by Szent-GyΓΆrgyi [30]; and that was observed not long after his proposal (see [24]). A vivid demonstration of interfacial water hundreds of microns thick next to the surface of a hydrophilic gel was presented by Gerald Pollack and his team at University of Washington Seattle [31] (see also [32, 33, 34]), which excludes microspheres as well as other solutes such as proteins and dyes, and hence referred to as an β€˜exclusion zone’ (EZ). Del Giudice and colleagues [25] suggest that EZ water is in fact a giant CD stabilized on the surface of the hydrophilic gel. As coherent water is excited water with a large collective of almost free electrons, it can easily transfer electrons to molecules on its surface. The boundary between fully coherent interfacial water and normal bulk water becomes a β€˜redox pile’. In line with this proposal, EZ water does have a potential difference of –100 mV to –200 mV with reference to the bulk water, and can act as a battery [34, 35]. Pollack’s explanation for the formation of EZ is based purely on classical physics, and converges with Del Giudice’s quantum fi eld theoretical explanation. This con- vergence between classical and quantum description is itself a sign of quantum coherence 7 WATER THE MESSAGE AND MESSENGER OF LIFE – SUPERCONDUCTING PROTON CURRENTS The core chemistry of life is reduction-oxidation or redox reactions that transfer electrons between chemical species. The movement of electrons is nothing if not an electric current. However, water electricity is special in that it also involves the movement of positive charges, i.e. protons [36, 37]. Water conducts protons by β€˜jumping’ down a chain of water molecules connected by hydrogen bonds (Fig. 5). A proton leaps on one end of the chain, and a second leaps off at the other end, while electrons are displaced in the other direction. This is much faster than an ordinary electric current involving the fl ow of electrons. Structured water confi ned in carbon nanotubes less than 5 nm in diameter was demonstrated using high resolution transmission microscopy accompanied by parallel modelling with a Hyperchem software package. The water appeared completely different from that confi ned in larger nanotubes [38, 39] (Fig. 6). I suggested that water confi ned in the small diameter nanotube, being more ordered, could be superconducting because proton jump-conduction could occur simultaneously down mul- tiple chains of hydrogen-bonded water molecules [40]. Later, Fullerton and colleagues offered a convincing model of liquid crystalline 6-member diameter nanotubes of water interwoven with the triple-helix molecules of collagen molecules in the collagen fi bres [41] (Fig. 7) reminiscent of those identifi ed in the small diameter carbon nanotubes; suggesting that these water structures in the extracellular matrix could also be superconducting [42]. It has been known since the 1970s that collagen supports jump conduction of protons and proton conductivity goes up exponentially with water content. Bardelmeyer [43] found that electrical conductivity in bovine Achilles tendon is fully determined by hydration, and the current is primarily carried by protons at water contents up to 45%, and by small ions at water contents beyond 65%. Between water contents of 8.5% and 126%, conductivity went up eight orders of magnitude. He also estimated that pure water’s dissociation constant is 10 -5 that of absorbed water; i.e. adsorbed water is more likely to let go of protons. Similarly, Sasaki found that the conductivity of collagen increased markedly with water absorbed – at an exponent of 5.1–5.4 – between a water content of 0.1–0.3 g/g [44], suggesting that continuous chains (of fi ve or more ordered water molecules) adsorbed in collagen enable proton jump conduction to take place. As seen earlier, the proton is in a delocalized quantum state even in bulk water under ambient conditions. This delocalization has been confi rmed recently for water confi ned in range of hydrophilic gels (reviewed in [45]). Delocalized protons mean jump conduction can be very fast indeed. Nafi on is a synthetic polymer used as a proton exchange membrane. Its chemical structure is a hydrophobic backbone with hydrophilic side chains. When hydrated, it forms channels of inverse micelles with hydrophilic groups facing the cavity and hydrophobic groups facing out. This structure is a good model of the living cell. The interstices between fi bres of the cytoskeleton and cytoplasmic membranes form inverse micelle nanospaces and channels that drastically alter enzyme/substrate relationships, often greatly enhancing enzyme activity compared with bulk phase thermodynamic models that still dominate conventional cell biology (see Chapter 18 of Living Rainbow H O [10]). 2 When Nafi on was drawn out into fi bres by electro-spinning, the proton conductivity of fi bres with diameters >2 ΞΌm was similar to the bulk Nafi on fi lm ( ∼ 0.1 S/cm). However, when the fi bre diameter was <1 ΞΌm, proton conductivity rose sharply with decreasing fi bre diameter and reached 1.5 S/cm for the 400 nm diameter fi bre, an order of magnitude higher than the bulk Nafi on fi lm, or silicon, a semi-conductor. Conductivity of the fi bre also increased a 100-fold as relative humidity rose from 50% to 90%; in comparison, conductivity of the bulk fi lm increased only 10-fold [46]. The inverse micelle model may be even more relevant to the extracellular milieu of multicellular animals, which is traversed by collagen fi bres consisting of fi brils interwoven with nanotubes of water (Fig. 7). These water channels aligned with collagen fi bres are most likely the anatomical cor- relates of the acupuncture meridians of traditional Chinese medicine, as I and David Knight fi rst suggested in 1998 [47]; the hypothesis is still much alive and untested [48]. What one needs to imagine are proton and electron currents fl owing inside the cells and over extracellular distances, delivering physical and chemical messages concerning the redox status, setting in motion the requisite core chemical reactions that restore local and global energy balance (and also the peripheral chemistry that forms the basis of the highly nuanced passions and feelings that make life so exciting for organisms). 8 THE ELETROMAGENTIC LANGUAGE OF CELLS AND MOLECULES Finally, how do cells and molecules actually fi nd one another? Conventional wisdom says hormones and receptors, cell–cell recognition molecules, and lock-and-key principle for molecules that some- how bump into each other at random (see current authoritative textbook Molecular Biology of the Cell [49]). Actually, there is substantial evidence that ...
 

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Inverse square law?

You are now living in the microwave oven.

Dr. Jack Kruse explains:


If you cant use time to.listen maybe jump up to 1:00:00 , about an hour in he gets into 5g pulsed weaponization and its effects electrically on your body and mitichondria.

Wuhan flu? Nope, its pulsed electromagnetic radiation so you can snapchat muffagas!!!
 

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Everytown for Gun Safety found that in 2020, the number of gun-involved road rage incidents that ended with death or injury almost doubled to 42 per month, compared to 22 per month in the four years previous.

Crazy on aeroplanes seems way up.

More kids suicide than covidcide.

Jack kruse predicts as 5g heats up the crazy will intesify... I'm watching him be right.
 

Panzerhund

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When people are suffering and dying, is that god's work also or are you going to blame that on a scapegoat?
My dear sweet summer child!

Does God create war and famine?

Does God create parents who abuse their children?

No!

People are at fault for every single problem with the world.

You are blaming God for things that people do to one another.
 

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Run this up to 20 minute mark if you in hurry.

Mitochondrial disfunction or failure to produce cellular energy is killing you.

This guy is blaming HFCS and copper depletion... fascinating@

 

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Light water and magnatism baybay!!!!
 

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85% of disease is a mitochondrial dissregulation?

Fix your mitichondria!

Doug wallace.

Abstract
The unorthodox genetics of the mtDNA is providing new perspectives on the etiology of the common β€œcomplex” diseases. The maternally inherited mtDNA codes for essential energy genes, is present in thousands of copies per cell, and has a very high mutation rate. New mtDNA mutations arise among thousands of other mtDNAs. The mechanisms by which these β€œheteroplasmic” mtDNA mutations come to predominate in the female germline and somatic tissues is poorly understood, but essential for understanding the clinical variability of a range of diseases. Maternal inheritance and heteroplasmy also pose major challengers for the diagnosis and prevention of mtDNA disease.
 
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