EMF 4: WHY MIGHT YOU NEED CARBS FOR PERFORMANCE?

   



HOW DOES THIS ALL WORK TO MAKE ATHLETES THINK THEY NEED CARBS?

 

With chronicity of poor decisions built in from poor ATP recycling,  (low brain dopamine) eventually, the body will lose its endogenous reference point. The brain is so slick in quantum computing, it can even adapt and rewire to use the molecular clocks in other organs when the SCN is blinded by modern life’s electron loss temporarily.  However,  as damage mounts, with time that system fails too. The net result in modern life is a slow insidious loss of endogenous bio-chemical control functions becoming increasingly out of sync, not only with the Earth’s resonance frequency, but also with our internal molecular clocks that coordinate physiologic functions body wide. You learned about them at the end of EMF-3, they are called CCG’s.

 

For example consider the real cause of auto-immunity: the body loses the ability to recognize what is “self” and what is “not self,” as it loses ATP function in the guts T cell’s in the GALT, which tell B cells in the GALT when to precisely turn off antibody production to a food antigen, at the correct molecular time. When the timing of this reaction is off, the result is an autoimmune attack on its own cells.  If you also happen to be a poor ATP recycler, you might use up all your methyl groups in the ATP-CP system and this further pushes you to any AI you can imagine.

 

I hope this begins to raises a few more thoughts for you to ponder now. Do cells shift their internal contents to favor certain reactions at particular times?  We have no idea because modern science is not asking this question because they are unaware of it.  How have the molecular sizes of toxins shifted over evolutionary time?   Could this be a cellular response to crowded target cells and more complicated cellular bio-kinetics of metabolic pathways?  We don’t know the answers to the questions because modern science (especially obesity literature)  remains in the dark over these factors and does not even realize they maybe the biggest factor in the equation of disease reversal.  I began to question these things when I was re engineering myself, and what I found was enlighten to my knowledge.

 

TRUTH BOMB: Timing matters more than what we eat.  If your clock timing is off you will never get to optimal. This is why circadian control must be restored before you alter your diet or begin to exercise. If you do not follow this you will never restore the ability to easily recharge your mitochondrial batteries using the D-ribose pathways. You will always rely on the two other less efficient ATP recycling systems,  and you will suffer inefficiency for energy, sleep, and have, muscle pain after most activities. We need better mitochondria before we begin to stress them further. This is why it is a cornerstone of the Leptin Rx.

 

TRUTH BOMB: Biologic reactions follow the same relativity regarding time. This cellular theory of relativity is found in levee one of the QUILT. It is, that important. It is also the reason why biochemists, researchers, and doctors seemed to be stumped by the causes of modern neolithic diseases. Most people think the problem is tied to diet, exercise, or laziness. They never consider the effect of how the timing of these reactions is set.   It is set by the circadian clock of the brain, and transmitted to every other cell in the body.   Today we have epidemics in obesity, cancer, diabetes, stroke, fertility issues, and many other neolithic diseases. They are all connected to a loss in the ability to account for time for proper biochemical reactions. The cause is because we are bathed in a sea of artificial light, man made EMF, and nutritionists who advocate for the electron poor diets. Something ubiquitous has to be behind our modern neolithic diseases, because epidemiology has established that epidemics are not caused by genetics. They are due to epigenetic effects that appear globally over a short evolutionary history.

 

THE TAKE AWAY:  When timing is off molecular crowding begins to accumulate within a mitochondria and with enough time, chaos ensues in the cell to destroy cellular signaling.

 

Chaos in space is called entropy, and in chaos in molecular biology is called inflammation. Inflammation is positively charged, and inflammation leads to more mitochondrial inefficiency, and loss of electron chain transport efficiency. When we lose energy we lose the ability to run processes in cells. This results in a loss of cellular signaling and once this happens all types of chaos ensues. This is how all neolithic diseases begin and progress to things like cancer and infertility.

 

When our brain can’t tell time neither can our cells; this implies we can’t sense our external or internal world correctly, and the result is disease.

 

We lose our intuition and our brain dopamine levels fall and our hormone panel gets destroyed. Cold Thermogenesis helps slow your electron loss while your “new behaviors” like Epi-paleo Rx, EPCOTx, Leptin Rx, grounding, avoiding EMF, increasing your personal magnetic field to deliver more electrons per unit time you are alive, and this allows you the “time” to recover from your energy deficit to refill your inner mitochondrial membrane with electrons to fuel ATP production to restore health.
This is the CIRCLE OF LIFE.

 

If you want to see step one in reversal of your current problem, read this link here.

 

Even a 5th grader knows what is best for them.

 

BRAIN/TIME SUMMARY:

The control of time in the brain is codified in three dimensions. Light, dark, and by electo-magnetic cells in our hypothalamus that pay attention to the Schumann resonance of the earth’s magnetic field. When the clock’s measurements are off kilter for any reason, we get resultant low dopamine levels in the brain and an altered hormone panel. Modern life has brought to us, ubiquitous artificial light and constant pulsed EMF’s over the last 100 years. If you look back at Brain gut 11, I spoke about the effect of light over diet in the human brain. 48% to 10 % neural tracts are allocated to photons over food electrons. Light and dark are two just two dimensions of how the brain tells time.

 

Just like a watch has three hands, an hour, a minute, and a second hand, our SCN has three as well. One for light, and dark, and another that tells us about the changes in the magnetic resonance in the environment. That frequency is codified by magnetic cells in our SCN, and the harmonic output is found in the alpha waves frequency of our brain waves. These waves control the circadian cycle and coordinate organ function. If anything blocks any one of the hands that tell time, we see changes in the clock, and we immediately frame shift electron flow in our mitochondria. That energy loss decreases the charging ability of our mitochondria to main cell membrane gradients. When we lose the charge of our batteries, disease soon follows. Light, dark, and the Schumann resonance allow us to yoke all our circadian cycles to our present environment. A poor diet just makes things worse, by causing more electron leakiness in the mitochondria decreasing our ATP levels even further. A diet that has more glucose in it because you eat it to fuel work outs, will cause further electron loss, and further decrease ability to replenish ATP from the best source, beta oxidation.  When you do this over and over and over, again you begin to believe you need carbs to fuel performance and endurance activities.  You do not.  The answer is found in the most chemically reduced pathway of life, the PPP.

 

So you maybe asking, can the brain or organ clocks be reset, after we screwed them up with carbs and crossfit?

 

Yes, I believe our chronotype can be reset. I spoke about cycloset in the EPCOTx webinar. The Leptin Rx uses food to do it, by altering your epigenetic switches, the hormones like leptin, eicasonoids, and cytokines. The Epi-paleo Rx prescribes a diet loaded in electrons from animals that have swam their whole life bathed in electrons from the oceans. Modern humans need electrons more and more everyday, because modern life steals them faster than we can replace them. Adrenal Fatigue Rx helps you stop leakiness at the PVN in the brain. I have given you many tools on the blog already to help change your epigenetic switches already. You just did not know the WHY. Now that you do, maybe, you might begin to implement the HOW, now.

 

Time is our most valuable asset. I think I have laid that out here. This all implies that we can reset our epigenetic switches as well if we begin now. We can alter our chronotype if we understand the “WHY“. Once you understand the why it makes the “HOW” easy to put into action. There are other Rx’s yet to come are also part of that “how.” Right now I am just shining light on the “WHY.”

 

TYING IT TOGETHER:

 

GEEKS: So the first thing a cell would see in an earth day is a period of day and night and the earth’s magnetic field. It also has to eat to make energy and it also has to control its own cellular division. So in essence the circadian cycle has to “yoke” to the metabolic cycle and its growth cycle. When it is night time, the cell becomes more reduced chemically and electrically. The chemical reduction is measured in something call TAN. (total adenine nucleotides) The electrical reduction is measured by something called the zeta potential.

During a low redox time, cells are usually recycling their components using autophagy (sleep). During the day while energy is being made to explore the environment, the cell is more oxidized because of increased leakiness of the mitochondria. Another interesting coupling occurs between the circadian cycle with the cell cycle. They are linked via the PER 1 and PER 2 genes. PER 2 directly effects the cell cycle in mitosis and also alters our response to glucose and carbs!!!  (Another reason why light, EMF’s and timing alters glucose metabolism directly.)

Mitosis is the phase in the cell that occurs just before cell division to generate an offspring. The mammalian period 2 (PER2) gene plays a key role in tumor growth in mice; mice with a mPER2 knockout showing a significant increase in tumor development and a significant decrease in apoptosis (levee 19 ). This is thought to be caused by mPER2 circadian deregulation of common tumor suppression and cell cycle regulation genes, such as Cyclin D1, Cyclin A, Mdm-2, and Gadd45±, as well as the transcription factor c-myc, which is directly controlled by circadian regulators through E box-mediated reactions.   E-box reactions are the chemistry that controls telomerase and our longevity. I mentioned these in some detail at Paleo Fx but it fell on deaf ears there, in my view, because they did not have the perspective of these EMF blog’s as yet. This means that sleep is tied directly into to cell cycle functioning and directly into cell mediated immunity at some deeply important level. That level is the expression or repression of telomerase which controls telomere lengths.  It appears that sleep directly effects the chronic diseases of aging and likely plays a role in all neolithic disease such as cancer development.  This means timing is huge for aging, performance, and longevity.

 

DEEP CIRCADIAN GEEK FEST REVIEW:   Adenosine opens the door to sleep, but the alpha waves created in the SCN have to be present at the right time to allow it recycle ATP and our proteins. Timing is critical. This is why circadian biology trumps all the biochemistry pathways in books.  It also completely explains why every human gene has a CCG in its transcriptional promoter region.   What good are the biochemical pathways if they do not occur when they are supposed to?   Alpha waves are the guardian of properly entering circadian cycling in the brain. When the alpha wave resonance is altered because of the frequency of certain EMF’ present,  this throws off all the nanoscopic precision required in biochemical reactions everywhere in the cell.

When this occurs in the mitochondria we lose maximum power. We learned in the January webinar that the mitochondria produce four times the amount of kilo-joules per unit of water that we need before we see abject organ failure.  Organ disruption of failure begins at 58 kiloJoules based upon data we have today from physiology.  When mitochondrial function falls below the 50% efficiency ratio, that we discussed in the December 2012 webinar, we begin to see cellular evidence of molecular crowding and this “throws” biochemical reactions “off kilter” in every cell of our body because this circadian cycle is “hard wired” to the growth and metabolic cycle of all cells. They are linked via the PER 1 and PER 2 genes. PER 2 directly effects the cell cycle in mitosis. Studies in animals and plants suggest that cryptochromes play a pivotal role in the generation and maintenance of circadian rhythms. Cryptochromes (CRY1, CRY2) are evolutionarily old and highly conserved proteins that belong to the flavoproteins (B vitamins) superfamily that exists in all kingdoms of life.

Cyptochromes are found in the light transduction pathways of all mammals including man. In, EMF 1, hopefully you saw this in the video I asked you to watch in the beginning of the blog. If not look at this shorter video.

In fruit flies (Drosophila), cryptochrome (dCRY) acts as a blue-light photoreceptor that directly modulates light input into the circadian clock, while in mammals, cryptochromes (CRY1 and CRY2) act as transcription repressors within the circadian clockwork. Transcription repressors are elements that directly alter the transcription of mRNA and all protein synthesis in every cell that uses it. Some insects, including the monarch butterfly, have both a mammal-like and a Drosophila-like version of cryptochrome, providing evidence for an ancestral clock mechanism involving both light sensing and transcriptional repression roles for cryptochrome. Cry mutants have altered circadian rhythms, showing that Cry affects the circadian pacemaker as well. Drosophila with mutated Cry exhibit little to no mRNA cycling. Recently scientists have actually spliced, and moved the human cryptochrome gene to these mutant flies and they restored their ability to sense magnetism and restore their molecular clocks of these insects proving definitively humans sense magnetism.

 

Today’s blog shows you WHY that ability is a BIG DEAL.

 

So you might be asking how does the cryptochrome tie directly into the main cell cycle gene PER 1 and PER 2 to cause disease? Well, the insect experiments showed us a point mutation in Cry-b, which is required for flavin association in CRY protein for functioning, results in no PER or TIM protein cycling in either insect. You might be shocked to hear that cyptochromes exert their biologic effect using a photo-electro effect on the flavin proteins in the cryptochrome.

Einstein already proved that light bends in relation to gravity and to time in a jungle in Africa in 1922 with the help of Eddington. It seems we now have evidence the our environment transmits quantum effects, or what we call quantum sensations, that our quantum computer (brain) pays strict attention too to recreate our reality in space/time.   It implies that our current idea of time is really a quantum sensation and not a real reality at all.  I know that just hurt your head, but it is true.  I believe this will become obvious to many in biology.  In EMF 5 you will see a nuclear physicist bring this point home right in your grill.  Quantum biology is no longer a physics problem.  It is a huge problem for you and evolutionary biology to deal with.

Why has this all remained a mystery to science for so long?  Quantum effects have always been in the domain of subatomic particles and not the macroscopic parts of life. Life’s mysteries have always been studied using biochemical equations, with the belief that the effect of physics is already built into those equations. Well, up until now one has thought, just maybe that time was relative to the very biochemical equations themselves,  to directly alter energy production. Remember E=MC2. Light and mass are both affected by electromagnetic fields of all types!!!

 

SUMMARY:

This is evidence of evolutionary change in the how the molecular clock was refined in higher animals (eukaryotes) after the K-T event. Post K-T, is when the mammalian clade exploded onto the Earth’s stage. As chronologic earth time has elapsed, evolution has simultaneously sped up, implying that accurate time keeping in all cells becomes more important as life evolves to maintain optimal ATP production. This means proper and precise yoking of time is quintessential for survival, if you’re an animal that is going to be able to accurately account for cell growth and the cell cycle. Today, we can no longer do that well past two decades of life, because of the epigenetic changes we have forced upon the world. We have altered natural light signals, increased EMF signals to ridiculous levels, all while the Earth’s magnetic field has declined according to US Geologic surveys.

These three things have caused a quantum change in how we tell and perceive time and the result is neolithic illness because these mistimings are directly related to the cell cycle via lower ATP levels.  It appears if we do not get the message soon we are all headed for the 6th extinction event.
I hope this helps you understand how powerfully important molecular timing is to all life.   As life gets more complex on the eukaryotic tree circadian biology increases its effect on biochemical reactions.  Accurate timing of our biochemistry is our most valuable and critical asset in any disease reversal.

This is foundational biology for my Quilt document at my site; where quantum mechanics and physics teach you biochemistry can be frame-shifted very easily…….and why what is in the bio-chemistry books……maybe a big fallacy because the kinetics of the cells reactions are all relative to time.  Biology has a way of showing you its truths, even if you do not believe them.

 

The moral of the PPP:  What comes easy wont last you long, and what lasts you long wont come easy……….

 

You just have to keep your mind open to the things you may not know. All science is based upon constant discovery. When you discovered something then it becomes a new jumping point for the next journey.

 

CITES:

1. Circadian Feeding Drive of Metabolic Activity in Adipose Tissue and not Hyperphagia Triggers Overweight in Mice: Is There a Role of the Pentose-Phosphate Pathway?
Endocrinology 2012 153: 690-699
2. Dehydroepiandrosterone reduces preadipocyte proliferation via androgen receptor
Am. J. Physiol. Endocrinol. Metab. 2012 302: E694-E704
3. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265077/
4. http://www.kaganovichlab.com/uploads/7/2/5/6/7256268/ellis_-_2001_-_macromolecular_crowding_obvious_but_underappreciated..pdf
5. http://www.sussex.ac.uk/Users/ctf20/dphil_2005/CSNs/Minimal%20Genome/Bray1998.pdf
6. http://www.biochemsoctrans.org/bst/028/a193/028a193b.pdf
7. http://blogs.smithsonianmag.com/hominids/2012/05/chimpanzees-sleep-in-trees-to-escape-the-humidity/#ixzz2Hv9lnTZQ
8. Ober, Clinton; Zucker, Martin; Sinatra, Stephen T. (2010-05-06). Earthing:The Most Important Health Discovery Ever?
9. Dehydroepiandrosterone Inhibits Glucose Flux Through the Pentose Phosphate Pathway in Human and Mouse Endometrial Stromal Cells, Preventing Decidualization and Implantation
Mol. Endocrinol. 2011 25: 1444-1455
10. High glucose inhibits glucose-6-phosphate dehydrogenase, leading to increased oxidative stress and {beta}-cell apoptosis FASEB J. 2010 24: 1497-1505
11. Applewhite R. “The effectiveness of a conductive patch and a conductive bed pad in reducing induced human body voltage via the application of earth ground.” European Biology and Bioelelectromagnetics 2005;1:23-40
12. Chevalier G, Mori K, Oschman, JL. “The effect of earthing (grounding) on human physiology.” European Biology and Bioelectromagnetics January 31, 2006; 600-621
13. http://science.howstuffworks.com/humans-age-in-space.htm
14. http://spaceflight.nasa.gov/station/crew/exp7/luletters/lu_letter13.html
15.”Relativity and the Global Positioning System”, Physics Today (May 2002), at equation (2)
16. http://www.nature.com/ncomms/journal/v2/n6/full/ncomms1364.html (human magnetic sensing abilities)
17. http://en.wikipedia.org/wiki/Cryptochrome (how they work in mammals and insects)
18. http://www.cee.mtu.edu/~reh/courses/ce251/251_notes_dir/node3.html (MIT physics geek link)
19. http://www.oddee.com/item_96973.aspx (Sunrises in orbit)

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Comments

  1. How do you get in and out of the PPP pathway? How can we endogenously produce ribose without carbs?

  2. How do you get in and out of the PPP pathway? How can we endogenously produce ribose without carbs? Where can I read about how carbs make mitochondria leaky?

  3. Shilohman says:

    Wow, this to me is really the Unified Field Theory of Epi-Paleo. Thanks Dr. Kruse.

  4. All I can say is that THIS is the blog I’ve been waiting for.

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