QUANTUM ENGINEERING #25: DEMAR HAMLIN, JJ WATT, & LICTENSTEIN FERNING HAVE A LOT IN COMMON

A cardiac arrest is an acute loss of electric power to the heart.  When the heart fails rapidly what do we do?  We re-shock it to get it started.  The electrical shock restores the decentralized networks in us.  This is why adenosine is part of the ACLS protocol with AED therapy.

IS INTENSE RED LIGHT CAPABLE OF REPLACING AN ACLS DRUG?

SVT is a broad term for a number of tachyarrhythmias that originate above the ventricular electrical conduction system (Purkinje fibers). In cardiac arrest algorithms, ACLS tells us to use adenosine via IV push to rid the heart of this detrimental rhythm until the patient is not symptomatic.  Why adenosine?

Did you know red light from the sun creates adenosine normally in the heart when it is exposed to sunlight?

Modern humans rarely expose their skin to sunlight and this is one reason cardiac death is a leading cause of death in humans.  

IS THERE NOW EVIDENCE THAT INTENSE RED LIGHT can do THE same thing using the PER circadian gene system? Does this imply that red light is a drug equivalent?

YES.

Is there more to this circadian story you need to know? YES.

Adenosine-mediated increase of cyclic AMP (cAMP) is a core component of PER2 expression and PER2-mediated ischemic preconditioning of the heart.  This means sunlight creates a perfect circadian situation for oxygen in the heart and its conduction system.

THE KEY HISTORY LESSON

The most dramatic event in the history of the earth was the arrival of sunlight and its effect on oxygen on Earth due to photosynthesis.  Sunlight caused the great oxygen event. With sunlight, trillions of photosynthetic algae could now make oxygen, transforming the entire planet's atmosphere and setting up the perfect storm for the evolution of a mammalian mitochondrial world.

This study on adenosine, red light, and the heart shows, on a molecular level, that intensive red light therapy offers a better strategy for treating or preventing low oxygen conditions like myocardial ischemia.  Why?  Red light has no side effects but all drugs do.

In this paper below in an effort to find out why red intense light can do this, researchers developed a photonic strategy using optogenetics to protect the heart using intense light to target and manipulate the function of the PER2 gene which is expressed in a circadian pattern in the part of the brain that controls circadian rhythms. (Sounds like something Dr. Kruse would suggest no?)

You do know that sunlight is made of 42% intense IR-A light huh?

By amplifying this gene, the researchers using JUST LIGHT PHOTONS, found that it protected cardiovascular tissues against LOW OXYGEN conditions like myocardial ischemia, caused by reduced oxygen flow to the heart. Dr. Kruse called low oxygen situations pseudohypoxia. These are all associated with low NAD+ levels in cytochrome 1 and leptin resistance with low delta psi on the inner mitochondrial membrane.

They also discovered that bright light increased cardiac ADENOSINE, a chemical that plays a role in blood flow regulation and sleeps. Hey didn't Dr. Kruse just do a massive post on ADENOSINE last week on his FB page?  Yep.

Mitophagy contributes to mitochondrial quality control not only by removing damaged mitochondria but also by promoting the biosynthesis of new mitochondria. It has been demonstrated that there is a crosstalk between the mitophagy pathway and the mitochondrial biosynthetic pathway (10). Specifically, Plaikaras et al. established that mitophagy and mitochondrial biosynthesis are interfaced with each other to maintain mitochondrial homeostasis.

The implication of this work is there's no need to take PQQ, and other supplements, if your sleep is sub-par. Sleep and sunlight remain king and queen.  Sunlight controls the adenosine levels in humans

Hey, isn't leptin resistance a synonym for melanopsin dysfunction? Yes, it is. Tell me again how that works Dr. Kruse.

My Response: Blue light and nnEMF liberate Vitamin A from our cells and cell membranes to raise its presence in the blood plasma and this lowers plasma levels of Vitamin C and Vitamin D. When Vitamin is liberated by non-terrestrial light or trauma, it becomes an aldehyde that destroys the small molecule modulators of the mammalian circadian mechanism. PER1 and PER2 are light gears in that eye clock mechanism.

It raises the question what in the hell do PER genes do?

Cell hypoxia is controlled by the hypoxia-inducible factor (HIF-1).
Do you know the link between HIF 1 to sunlight and oxygen?  Light and oxygen-sensing pathways are linked on a cellular level in ALL mammals (Gu et al., 2000, Hogenesch et al.,1998, McIntosh et al., 2010).  Hypoxia-inducible factor 1⍺ (HIF1A), is an evolutionarily conserved transcription factor enabling cellular adaptation to low oxygen availability (Semenza, 2011).  Here is the kicker:  It belongs to the same protein family as the light-inducible circadian core protein Period 2 (PER2) (Liu et al., 2012).

HIF-1 is what the entire hypoxia series was about on Patreon.  Review those blogs sometime.

So when you're missing sun your cells sense your missing oxygen and HIF-1 goes up and PER circadian mechanism genes go awry.  The circadian mechanism loses its periodicity.  Remember what you learned on Patreon about periodicity?  Periodicity is a synonym for the circadian clock mechanism.  This ruins every cycle in the cell that relies on it.

Once the molecular clock in the eye and peripheral clocks goes awry the implications for many neolithic diseases spiral out of control. What are some of the Vitamin A proteins involved in this downward spiral?

They are called retinoic acid receptor-related orphan nuclear receptors or RORs for short. The RORs have several isoforms too called RORα-γ. These proteins are also under the transcriptional control of CLOCK/BMAL1 heterodimers.

CLOCK and BMAL1 are positive regulators of circadian gene expression, and PER and CRY are the NEGATIVE FEEDBACK LOOP regulators that operate under day and night cycles. These are the positive and negative feedback arms of the circadian mechanism.

They must be coupled properly to terrestrial light to operate well and control all growth and metabolism, protein synthesis, and hormone production and release. It also controls receptor biology. It controls EVERYTHING. If they are not properly coupled to the light and dark cycles the eventual results are the extinction of both sides of the feedback loop. So when sunlight is absent we lose control of the negative feedback loop of the circadian mechanism controlled by PER2.  This is what causes the NAD+ drop in mtDNA.  That is how all human disease begins. It is circadian biology that couples all the molecular clock genes in humans and the SCN of the eye drives the program and the major timekeeper.  The SCN as the metronome of biology loses accuracy as PER2 drops.  PER2 is critical in controlling the optical periodicity of the circadian mechanism.

Are heart rhythms are controlled by the circadian mechanism in humans?

Yes, they are.  The enzymatic flux of the entire TCA cycle is also controlled by it in the electrical system of the heart.  Cardiac arrhythmias are a leading cause of cardiovascular death in humans. It has long been accepted that life-threatening cardiac arrhythmias (ventricular tachycardia, ventricular fibrillation, and sudden cardiac death) are more likely to occur in the morning after waking. It is perhaps less well recognized that there is a circadian rhythm in cardiac pacemaking and other electrophysiological properties of the heart. In addition, there is a circadian rhythm in other arrhythmias, for example, bradyarrhythmias and supraventricular arrhythmias.

Two mechanisms underlie this finding:

(1) a central circadian clock in the suprachiasmatic nucleus in the hypothalamus may directly affect the electrophysiology of the heart and arrhythmogenesis via various neurohumoral factors, particularly the autonomic nervous system; or

(2) a local circadian clock in the heart itself (albeit under the control of the central clock) may drive a circadian rhythm in the expression of ion channels in the heart, which in turn varies arrhythmic substrate.

Remember the free decentralized lesson from my FaceBook page on 7/31/2019:

I said, "Classic Paroxysmal SVT (supraventricular tachycardia) has a narrow QRS complex & has a very regular rhythm. ... A rapid heart rate will significantly reduce the time which the ventricles have to fill.

The heart fills during diastole, and diastole is normally 2/3 the cardiac cycle. A rapid heart rate will significantly reduce the time that the ventricles have to fill. The reduced filling time results in a smaller amount of blood ejected from the heart during systole. The end result is a drop in cardiac output & hypotension.
With the drop in cardiac output, a patient may experience the following symptoms.

These symptoms occur more frequently with a heart rate >150 beats per minute as the ECG strip shows below:
Shortness of air (S)
Palpitation feeling in the chest (S)
Ongoing chest pain (U)
Dizziness (S)
Rapid breathing (S)
Loss of consciousness (U)
Numbness of body parts (S)

The pathway of choice for SVT in the tachycardia algorithm is based on whether the patient is stable or unstable clinically.
The symptoms listed above that would indicate the patient is unstable are noted with the letter (U) in a cardiac code situation. This can present outside a code situation when someone has a very low redox state because of a very poor environment linked to blue light and nnEMF toxicity. This mimics adrenal fatigue and brainstem pathology, sleep disorders, and eating disorders. Stable but serious symptoms are indicated with the letter (S) above.
Insert any 3G-5G city or environment. a \/, trauma, poor sleep = an acute or chronic adenosine problem.

HYPERLINK

What screws up sleep ultimately in decentralized networks in cells? Problems with adenosine at the brain stem level. Go look up what adenosine signals in us.  It is the biochemical signal that begins the sleep cycle in humans.  This is why ACLS uses adenosine to treat acute mitochondrial failure in the heart that results in SVT cardiac rhythms........guess what drug is used for cardiac tachycardias in ACLS?
ADENOSINE via IV push = a DEFECT IN PER 1 or PER2. SOUND FAMILIAR?

Light-deficient humans get electrical problems in their hearts before the disease begins that people can see and sense.  That is what bad rhythms mean in patients whose heart is still pumping but acting badly.  They are all light deficient, solar light deficient, and most of the time blue light toxic.

How do you like me now?

When the system teaches ATLS/ACLS/BLS/CPR recertification you can see where their focus really lies if you are paying attention. Pre-covid videos and protocols are available for you to review. Every variable has been subjected to intensive statistical analysis to increase the odds of survival, but there will be no mention of how a broken circadian mechanism leads to all codes covered by their protocols.  That includes myocardial infarction, clots, or seizures; which are the most common cause of acute arrest today.  To a decentralized mindset, you might think this omission of the circadian defect should invalidate the stats and protocols they regurgitate until you realize what perspective they play this game with.

For example, historically, a small child has been more likely to choke or ingest a poison than suffer spontaneous heart problems than an older child or adult. The protocols never take new data that the system is built around.  This eliminates new decentralized options and just keeps publishing ideas of treatment that are based on data that may have changed and has not been updated. No updates or changes for first responders are present, except for the new advice of not performing mouth-to-mouth resuscitation on kids. I wonder if we will ever acknowledge the elephant in the room, and change our dataset and actions or if organizations like the AHA, ADA, FDA, CDC, and USDA will continue to feed us garbage into perpetuity.

Why would you expect a centralized healthcare Rx to be set up to work for you based on their perspective on health?   Do you realize who is being harvested and bled dry by these beliefs??  The public is.  If you knew the sun fixes this and drugs induce many more problems than they solve you'd realize you really do not need most of what centralized healthcare sells you.

How does a centralized healthcare system operate?  Is it for your benefit or theirs?  In most cases, protocols are set up for the chronic profiteering of the system.

Centralized healthcare remains fully ignorant about how light operates in our bodies by design. The people who profit make the curriculum that the experts are forced to learn from organizations like the AHA, ADA, FDA, CDC, and USD so they can sell products, drugs, foods, and suncream to you because their advice is given to you when you visit the centralized system for advice. It is a giant financial feedback loop and you are the patsy. The decentralized healthcare system warns you with data (adenosine a drug in ACLS can be replaced by the red light of the sun to get the same effect for the heart)  that if you avoid the sun and wear suncreams the guys selling as the centralized solutions (Pharma/food/AHA/CDC/FDA facade) their profits rise while your health risks multiply over time. As the risks rise they are ready to wallet biopsy you as an inpatient next. The centralized circle of life explained.

I'm shocked you're shocked.

IS THIS ALL HYPERBOLIC TALK?

Does centralized medicine have direct evidence that is visual that we are built entirely from many decentralized networks?

What can lightning strikes of living systems teach us about life?

Lichtenberg figures are reddish, fern-like patterns that appear on the skin when a patient is struck by lightning. These appear to be a result of an inflammatory response to the electric voltage as the current spreads out causing ionization and heat effects and damage to the small subcutaneous capillaries.

It tells us more about us and less about light. We are photoelectric beings and the marks on us outline many of the decentralized networks operating inside our cells. https://www.frontiersin.org/articles/10.3389/fmed.2021.663807/full

SUMMARY

The fastest way to make Lichtenstein's marks vanish is to add red light back to the system.  It sounds a lot like how we make SVT vanish from heart rhythms, doesn't it?  This makes electrical sense when you understand what these ferning patterns are on the skin.  They are a sign of an electrical discharge in the body that has lost an acute amount of redox power.  Red light is the easiest way to recharge the body quickly so its addition to the skin will make the repair happen more rapidly.

As cite one below shows us, the new mRNA \/'s can cause sudden cardiac arrest and we had visual evidence of that recently in an NFL game.  Many of you will read this and not believe it.  I want to remind the skeptics of this reality that also occurred this year in NFL circles.  Remember when JJ Watt had to have his SVT treated after he was injected with mRNA technology?  What did they do to treat him?

VIDEO 

They had to emergently shock his heart back into a sinus rhythm because the drugs they gave did not work.  This is really bad news for anyone who took the government mandate seriously and complied with it.   Do you think this might have anything to do with why he is retiring from the NFL now a few weeks later?  I think Demar Hamlin's acute cardiac arrest on MNF in front of the US public is going to become a commonplace post-vaccine mandate.  JJ Watt's case tells us that you do not need trauma to induce an arrest.  A bad rhythm may come first before the arrest occurs.

Might the same prescription of using light to combat disease be important in helping someone overcome that centralized healthcare injury?  Does this Tweet video look normal to you?

TWEET

Mitochondriacs know that answer.

Do you?

If you are vaccinated, and you are a highly paid professional athlete, you should be screened for the SCN5A polymorphism and Bruguda syndrome.   There are 4 known common polymorphisms of the SCN5A gene related to BrS, including R34C, H558R, S1103Y, and R1193Q. In my professional athletes who were forced to get the jab, we always suggested this hack.  The Rx for it was "endogenous and exogenous melanin renovation therapies" done in the offseason to prevent some of the things you saw last NFL season.  If you are a vaccinated human with heart rhythm abnormalities, you should ask your cardiologist to screen you, too, even if you are not a million-dollar athlete.  Most centralized cardiologists have yet to learn about this decentralized wisdom.  In 28 NFL cities, I have asked many of them about this science and got blank looks.  That explains what happened to JJ Watt and Hamlin.  

These SCN5A polymorphisms often decrease the expression of sodium‐channel proteins and alter gating properties, resulting in prolongation of the QRS duration and slow conduction in the heart, making sudden cardiac death and rhythm changes more common in the face of mRNA damage = higher cardiac heteroplasmy in young people = unexpected morbidity and mortality and sudden death 

CITES

https://twitter.com/vascohill/status/1613610308140138496

https://twitter.com/P_McCulloughMD/status/1613685112033394689

https://academic.oup.com/ehjcr/article/5/3/ytab054/6154461

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520649/

https://nigms.nih.gov/education/fact-sheets/Pages/circadian-rhythms.aspx

https://geardiary.com/2011/06/17/meet-winston-kemp-lightning-strike-survivor-and-lichtenberg-figure-owner/

https://www.cell.com/cell/fulltext/S0092-8674(13)01521-3