Sunday, September 26, 2021

Diver elongation of telomere



The latest link

My comments are in italic.

 

It is worth examining this since it will have theoretically similar performance to HHP-HBOT and have lower cost as ordinary air can be used instead of oxygen expense. It matters not that the HHP-HBOT effort may be faster. A quick design of the simulation machine says that the costs are returns on the machine, attendant (rs 20000 per annum including benefits) and electricity, thus price of Rs10 per day of 2hr sessions can be achieved per 4 patients per day every 10 machines, attached to a hospital as shop. The attendant can run a shop filled by many machines, reducing the cost by that factor. Such machines will be useful for persistent diseases targeted for repeated treatment. These abstracts say that divers encounter HHP with ordinary air and a machine proposed have reasonable chance to work.

 

1.           Abstract

Many cross-sectional studies have tried to assess the in vivo effect of oxidative stress on organismal aging in general and on telomere length dynamics specifically. Here we followed telomere length dynamics over a 12-month interval, in divers exposed to intense hyperbaric oxygen in comparison with an age-matched control group. Both groups were exposed to extreme physical activity, as well. Among the divers following the oxidative stress, significant telomere elongation was observed in granulocytes and naïve T cells, but not in memory T cells and B cells. Telomere length in granulocytes was mildly elongated in the control group as well, a finding that may relate to the extreme physical activity to which they were exposed. While telomere elongation in naïve T cells may be attributed to telomerase activation, we suggest that in granulocytes the elongation results from undifferentiated hematopoietic cells carrying longer telomeres that repopulate the peripheral hematopoietic compartment. This event might be accompanied by enhanced cell division within the repopulating pool. Since the aging of mammalian tissues can be attributed in part to the reduction in the replicative potential of self renewing cells, enhanced cell turnover under conditions of hyperbaric oxidative stress might be directly relevant to tissue and organismal aging.

Research highlights

 Telomere elongation in granulocytes and naïve T cells in divers exposed to oxidative stress. No telomere elongation in memory T and B cells in divers exposed to oxidative stress. Telomere elongation in naïve T cells may be attributed to telomerase activation.  Oxidative stress may lead to repopulation of the peripheral hematopoietic compartment.

 

2.          Abstract

Many cross-sectional studies have tried to assess the in vivo effect of oxidative stress on organismal aging in general and on telomere length dynamics specifically. Here we followed telomere length dynamics over a 12-month interval, in divers exposed to intense hyperbaric oxygen in comparison with an age-matched control group. Both groups were exposed to extreme physical activity, as well. Among the divers following the oxidative stress, significant telomere elongation was observed in granulocytes and naïve T cells, but not in memory T cells and B cells. Telomere length in granulocytes was mildly elongated in the control group as well, a finding that may relate to the extreme physical activity to which they were exposed. While telomere elongation in naïve T cells may be attributed to telomerase activation, we suggest that in granulocytes the elongation results from undifferentiated hematopoietic cells carrying longer telomeres that repopulate the peripheral hematopoietic compartment. This event might be accompanied by enhanced cell division within the repopulating pool. Since the aging of mammalian tissues can be attributed in part to the reduction in the replicative potential of self renewing cells, enhanced cell turnover under conditions of hyperbaric oxidative stress might be directly relevant to tissue and organismal aging.

Saturday, September 25, 2021

Hibernation



latest link            next link


There is a reason why club 3 technologies together in that not only wish death is achieved, something new is made that removes the infinite boredom that may result. The two technologies beyond amrit for infinite life, within current physics and hence more than sci-fi (tech fi in my lingo) are, 

1. Wish death or amrit, must be first to utilize later technologies

2. Hibernation/Astivation to travel the solar system using realistic technologies

3. Brain download for light-speed travel without time elapse

#3 can be way down in the future with MIT technology to greatly expand the folded brain. It is #2 that requires research, continuing now, to perfect. We understand cold hibernation some. It became evolution engineered to allow animals to migrate towards the poles. The two poles are distant on the globe, hence the fauna that developed in the sea and on land are distinct. The north pole has polar bears and walruses for example. The south pole has penguins and eels for example. Evolution had to independently develop the mechanism for hibernation and tissue preservation on freezing.

The first overarching statement I make is that all cold hibernations examined so far, as well as extensions imaginable, will never be applicable to warm-blooded creatures like us. Stating this, I deny every sci-fi so far. The point is the regeneration of blood after freezing is not possible on thawing. Not only do I condemn sci-fi but all post-death cryopreservation which preserve with freezing.

Cryopreservation is not just sci-fi research, but immensely important in organ donation. It is estimated that only 20% of people get donations usefully while they wait in queues and die not only because of donor shortages but transportation losses. And here I claim that cryopreservation is not possible!

So is it the end? Not really because there exist warm-blooded animals that hibernate! The process has a different name - astivation. The best model is the Madagascar lemur! The evolutionary reason is the same - food sources in the predictable part of the year dry up. Only tolerated by animals that can genetically activate it! How does it work and who researches it?

In it, the body temperature drops, say 10fahr, the animal becomes lethargic, and heartbeat drops from the usual 180 to single digits. Unlike cold hibernation, the animal quickly recovers within a week, restores heart and breathing, and then rapidly drops to a torpor state again. Astivation itself lasts several months with a weekly brief waking up.

I think the wake-up episodes allow the body machine to be kept up, even while the lemur sleeps. I can imagine humans in the situation of multi-annual sleep with their bodies being woken up, and even monthly restore to expel wastes and restore hyper-nutrition food (lemur solves food issue by gorging when food is plentiful and storing energy as fat in their enlarging tail, thickens 40%, lemurs called fat-tailed in local lingo).

Who researches astivation?

video: Doing research on lemur

If you can afford it


 The latest link

This is not a simple logical essay, but the result of very hard work over twenty years, witnessing the dawn of amrit, hoping that I can distinguish it and partake in it. Belief in any religion is not criminal, finding ANY support for any distinct unobjective argument based on whatever you believe is criminal. I say above from 20 years of hard study. Science as rational skepticism RS is extended to TRS by me to define engineering as triaged RS. Evolution is viewed as natural engineering on life, solving polynomial and nondeterministic polynomial problems using time and biological sexual inheritance, intermittent & natural selection. 

Undo Aging - normal middle class or better

 

Aging undo is the oldest desire of humans, recorded since Gilgamesh of Mesopotamia 4000 years before. Since then, conscious and nasty stupid criminals have routinely attempted to sell based on guarantees to arrest the pace of aging. I pull no punches – every such person, especially claimants associated with the religion of ALL kinds is a criminal. Note that my introduction itself delineates who isn’t and is worth spending time on. If you disagree then fuck off, this is not for you.  

 

With this definite position, what remains? Simple logic states that some axioms must remain that are basic to your argument, these then define a new religion. True, except that one can define some axioms by statements that are falsifiable, but true objectively, italicized to indicate the word phrase has an extensive philosophical meaning needed to understand beyond lazy conversational usage, for example, paradigm change. Objective truths imply experimental repeatable. Clearly, all historical facts cannot be objective. That aging can be addressed without any presumptions is hard but required.

 

Science is a collection of objective truth. Thus, it has the property of being falsifiable. Positively, it is rational skepticism. It can be viewed as a collection of models on mathematics, objects, or animals. I assert that one can understand nature, behavior, life by science. Life here means creation (evolution), progress (medicine), and aging.

 

These are four defining properties of evolution (triage, natural selection, intermittent, sexual duplication) that result in triaged evolution essential to obtain a result in evolution-reasonable time. Imperfect consequences happen because evolution success is by choices resolved to favor objective survival over usefulness for humans. It explains while whales, elephants, and naked molar rats live so long, free of disease, we don't - it is all triage, not the stupid choice of any god.

 

Basis of triaged evolution?


Coming up with organs for new chemicals is a slow non-engineer aspect of evolution. Much better for survival is an unusual use of existing chemicals. It will propagate by improved survival of those capabilities. But there is a problem, which system gets the chemical first if use is shared.  Given the style of evolution, it is easy to see that the organism which divides unequally will prosper over communistic equal division if the user1 is more important for immediate survival than the user2.

 

As aging undo bioengineers, we do not have to ape natural evolution blindly. Let us pseudo-argue from D3 and K2. The body can use the D3 vitamin as making calcium precipitate more on bones and dissolving its precipitate in vascular paths. Naïve evolution prefers bones as the strength of bones improves survival (fix varying amounts of osteoporosis starting osteopenia). The vascular calcium creates only osteoarthritis, painful but not useful in survival. K2 vitamin (best as MK-7) acts like D3 but does not do bone fix like D3. So a diet good in d3+k2 is a lot better for patients to escape osteoporosis and osteoarthritis, no matter how evolution proceeded in the patient. Given D3 is a fat-soluble vitamin, it can be eaten every day, weekly and monthly, depending on the patient. I take all K2 and some D3 per day, rest every week. D3 poisoning happens but very rarely, the current dosage max of 30,000 IU per week was routinely done at 500,000/month IU in the sixties. It is hard to self-poison. Typical extreme dosage results in D3 high, like president Trump's speech in Florida, after releasing from Corona-19 infection.

 

I am a Ph.D. engineer, not an MD. The complete undo Aging is viewed by many native (America) persons as a subject for western MD, but I strongly differ. The entire undo Aging subject is essentially genetics and immunology, last being a specialty unknown to usual MD or MBBS to any depth. The mRNA forms a basis, just as genetic engineering does. The entire subject is better-called cell engineering, and that will be used by me hence, with undo aging being my goal and I posit that cell engineering does that. All structures bigger than a cell is where medicine starts.

 

Brand of suggested medicine

 

It is slightly unusual since I do not condemn methods. I do not consider any style to be free of errors but recommend all medicine not based on only cure but based on usual unintended errors too. By that belief, homeopathy is not criminal but excellent only whenever a placebo is useful. Legal limits must be placed on various formats to show experimentally that all patients that subscribe to a view benefit objectively. All practitioners are faced with a time limit and all practitioners are punished for patients not cured within diagnosed intervals at the start. It is the practitioner’s responsibility to refuse patients unlikely to benefit. People that benefit from placebo are afflicted with a transient disease. The goal is to separate them into genuine disease and transient diseases. Time is lost in genuine cases but to only recoverable extents.

 

Short statements to prevent bothering some people, fuck off if this bothers you.


Ayurveda and likes have a long history including a modern period free from the external disease-vector theory of causation and cure. Not all diseases are external organisms caused and this is exactly when allopathy fails, with excellent treatments but no cure for heart disease, diabetes, osteoarthritis, cancer, aging, etc. 

 

Undo aging is about compressing old-age decrepitude and life extension?


Undo aging with cell bioengineering is likely a cure for these chronic diseases, aging, and cancer as well. Apart from in vivo methods, cell transplantation CT techniques will be developed that can slowly, several cells at a time, will be able to extract in vivo cells, process them in the lab and restore them pipelined into the sampled organ. This is then the new medicine I wish to experiment with. But the current essay is on causation and cure, pointing out the failures and cures beyond excellent treatments of modern western medicine. I wish to complete this section with what more to allow beyond western medicine even while stating that ALL talking about wholesomeness, top-down, executive-like, and quantum mechanics in health are meta-moron (condemned to be unfixable chronic morons) emfubar criminals.

 

Who to believe and why?


There is a small list of pioneers in aging who have two and more paradigm-changing developments in aging and will not be falsely drawn into support of any new aging method for abusive advertisement professional reasons without critical speaking of others in this list. They are Dr. de Grey (SENS, Methuselah, funding,…), Dr. Sinclair (resveratrol,  NMN, optic nerve grow, …), Drs.  Conboy(Original parabiosis,1920 correction test, …), Dr. Horvath (DNAm, Eutherian aging, …), Dr. Yamanaka(DNA reprogramming,Yamanaka factors). You can set up your own list but I suggest a very shortlist consciously searched and applied. You are certainly stupid if this essay is ignored by inaction. Do something, not necessarily as I suggest.


Aging basics?


Objectively increasing health span by 14 years is easy, says Dr. Sinclair. The good advice from all elders of long sleep, low stress, exercising, good fat-free food, and short infrequent feed habits will do it. The objective for him with mice model experiments, and additionally for me by analyzing the life span of my father. My goal is curing chronic age diseases first, lifespan later! Healthspan at least 150 years.


Only science axioms?


This entire essay builds upon the objective possibilities of two century-old interventional experiments of the lifespan of animal models of mice, rats, primates, and observational studies on humans. Calorie restriction, Intermittent fasting, and exercise. Benefits of calorie restriction and exercise are possible with chemicals, best helped by lower intensity CR and exercise. Or practice CR+Intermittent fasting+exercise only and no chemicals, but that limits you to 14-20 years.


There is one test described by Dr. Sinclair on mice. An experimenter-set divided mice into several groups and fed them at different times various classes of food. Then they waited for mice to die. Uniformly, without distinction of foods taken, the longest-lived were those who were fed just once in a small time slot even if the mice gorged equal amounts to those with several well-spaced feeds! I call it intermittent feed. Both he and his 81-year-old father have a big dinner, soup, and tea several times the rest of the day. They are both healthy lookers and act young! Perfect for aging scientists - apply to self and family first. 


Aging theory?


You need to clean up vesicles and oppose NAD+ decrement and decrement continuously rising SASP that continuously reduces NAD+. NAD+ booster chosen is NMN. Pterostilbene for vesicals. Fisetin+ to reduce CD38 in SASP. Know if working by energy level after November megadose of Fisetin (mayo protocol).


Recommended food?


Nothing makes a difference! Only meta-morons advise edible and forbidden! Diabetes defines my food. Has no food effect on aging. I have changed to big breakfast, small lunch and small dinner. But no one in the family is converted, will be willing negative controls! On the other hand, I wait November 2021. The point for me is I start in 4 days to see if the supplements I ordered, will stand for exercise. Apart from K2/D3 with no aging concerns, these are NMN and Pterostilbene for NAD+ increment and fisetin for SASP decrement.


Plan so far?


Assuming MIB-626 gets FDA2 approval and can be sold, it replaces NMN and Pterostilbene. If E5 is sold even within the USA, switch to it. Fisetin+ continues.


orthomolecular.org

Cell medicine


Sunday, September 19, 2021

Best one hour of your life

 



 

https://www.youtube.com/watch?v=BRFqPSy48b4

 

(1+ hour) The recent content in this talk between the two greatest scientists on aging is disruptive science for all non-scientists, answering even “What happens to earth with the conquest of death?” even though that is an audience question and not more than 1% of the aging seminar. The bottom line for Dr. Sinclair is “why do we have a pathetic physique, dead by even a chimp sharing an enclosure with us, if it happened, pathetic 10 finger hands in double, …”.To which I add “single heart even if all other organs have redundancy”. Our technology has solved some problems, but every fix has created newer problems. Will we ever get down from the treadmill? Or will those still on, ensure we don’t get off! To this, the other Dr, Lee, aged pioneer, summarizes

 

1.    Aging in the latest theory, has been pushed back billion years to the first unicellular life, all life ages the same way, genetically in each cell, be it plant, animal, bird, human. Sinclair’s theory of information points to cell death from errors in DNA repair.

2.    Aging is simplicity and elegance shared by all life.

3.    We can use yeasts, mice, etc. to model and learn about humans. Some animals (eutherians and also jawed vertebrates) model humans (science means modeling phenomena by mathematics, instruments, or animals).

4.    Aging is a disease, which can be arrested

5.    Even reversed as redundancy is obtained by an epigenetic layer over DNA which is intact regardless of age

6.    Chronic diseases are underlain by aging and may be cured, unlike modern medicine(allopathy) which can not handle chronic diseases without an organic cause. (Treatment yes, cure no).

7.    Next ten years (9 by me) will see disruptive changes revolutionize not just aging but the decrepitude of aging.

 

I stand corrected, the aging bounty is not just for exercise freaks but all. To live to a widely accepted amrit requires funds and fitness, though. Ando undoes aging will not be cosmetic. We are 65+, not 50+. Too many of my colleagues are dead, forever.

 

 

Friday, September 17, 2021

My Medicine as supplements

 


 

There is a natural order induced by expected effectiveness. It is also my first list in Liposome versions. Some supplements will be released by Sept. 30, and hence have to be preordered.

A why prefixes materials.

 

Liposomal Vitamin D3 & K2 - why?

I believe in triage evolution, with triage resolved to favor immediate survival. D3 fixes bones and cleans blood path, resolved by evolution to bones first triage. This means the blood path suffers from calcium deposits. Genetic history of evolution end. K2 also cleans paths but considers them first before bones. So, K2 is a good solution for all d3 sites but bones! So D3 for all forms and amounts of osteoporosis, and k2 for all others but bones! K2 in MK-7 form is considered best.

 

Liposomal Fisetin - why?

Aging has two chemical effects in parallel – NAD+ decrease and SASP increase from senescent (best considered dead) cells. NAD+ is needed for many reactions in the Krebs cycle. It is reduced by SASP, so cleanup of senescent cells is essential, this supplement does it largely, best by mayo protocol and also continuous use.

 

Liposomal NAD+ with Resveratrol LIPO  - why?

Best to compare Liposome as intravenous line add or like injections, even better since cell membranes are not a barrier, but some 20% loss in stomach or liver. Help is enormous in glutathione. Injected, NMN survives for a week after NAD+ conversion. Direct NAD+ has to be injected every day. Which of NMN or NAD+? Depends on the patient. Also crossing BBB. Small Liposomes make NAD+ better. The answer is really titration by the patient. That is why a 50% mix of NMN and NAD+ for 1 year is suggested

 

Liposomal NMN w/ Resveratrol LIPO  - why?

Allows patient to self-titrate. Four 3month periods select between pure or joint usage. Note that Liposome means resveratrol over pterostilbene!

 

I do not disclose specific places and dosages, so the above is very informative but way insufficient for use. Those who are interested should inculcate an MD and bioengineer like me conversant with chemicals used, dosages, right sellers, prices, and expected effects and timings.

Saturday, September 11, 2021

E5: expose the secret. How?

 

To the Gentlement named below,
 

E5: expose the secret. How?

Looks like real singularity, after intensive research, when marketed - USA first. Likely after FDA trial, in 1-2 years. To bio-hackers as me, buy+consume after FDA-1.

My questions are in this font.

3.    Solely to assert your time is not wasted, I belonged to Unix Group at Bell Labs and professor of computer science in Univwesity of Massachusetts pre-retirement.

WWithout knowing E5, here is what it really is. The story of young blood use is likely to confuse all who will try to understand E5, needed for many new types of research. That is one way to benefit from the work. Sinclair had a much better approach to his disruptive workbook royalties and greatly improved life, at Harvard and in Sidney. I do not think money drives Katcher, but it drives people who invested in him. I think his answer would be even smaller than mine!

The bottom is Drs. Conboy link, more believed than Dr. Katcher spiel! In any case, I have written to Dr. Sinclair, Dr. de Grey, and Drs. Conboy, beseeching them for clarification, why the young blood claimed.

Young blood does not reverse aging in old mice, UC Berkeley study finds

Insight 1: The DNA molecule has subsequences, both useful and evil. The epigenome sits over and shuts the evil ones off.

Insight 2: DNA marks (methyl) are not only markers of aging, but consequences of use! Removing them not only reduces bio age but makes you actually younger. The following story got to me (how?) that in the womb babies start with zero methylation, methylation advances at a normal pace, but is reset again to zero at birth! We undergo age reversal once anyway!

Insight 3: DNA never changes but epigenetic cover turns the gene off and on. Signal molecules in blood are the only way DNA information causes proteins to be built.

Insight 4: Katcher's work on breast cancer is essential to prevent cancers that will arise from poor reverse engineering.

Isn't expose E5 needed for rapid use in attacking for more cures in modern medicine, given only treatment of persistent diseases are possible.

 

Thursday, September 9, 2021

 


Understanding e5 development and excitement

 

            E5 has been tested in a joint paper of many authors including Dr. Katcher and Dr. Horvath as this link.

 

https://www.biorxiv.org/content/10.1101/2020.05.07.082917v1.full.pdf/

 

            Dr. Horvath in the list implies data is correct, references good, as per [me]. Every claim in proper science must be tied to experiments, distinct from all religions where a book is believed.

            The paper data raises a related and equally interesting question, which is why does plasma fraction treatment not reduce brain epigenetic age by the same magnitude as it does the other organs? 

The paper does read

(a) epigenetic aging is distinct from the process of cellular senescence and telomere attrition [me]

(b) several types of tissue stem cells are epigenetically younger than 

non-stem cells of the same tissue [me]

(c) a considerable number of age-related methylation sites, including some clock CpGs, are proximal to genes whose proteins are involved in the process of development me]

(d) epigenetic clocks are associated with developmental timing [me], and 

(e) relate to an epigenomic maintenance system [me].

 

Some process in all trillion cells is leaving behind a methyl group every time a C sugar has a phosphate bond to G sugar (called CpG islands) on the DNA. It happens in all cells but the brain and stem cells. Now Katcher believes that all communication in the body is by signal proteins. So clearly the mechanism is not damaged accumulation but programmed death. Trying to extend life is anti-evolution for our size – whales are the top predator in their food chain and live 300 to 500 years, or see elephants.

This data suggests that homeostatic maintenance of the body post-maturity is tied to an epigenomic clock process! As such, if plasma fraction treatment’s rejuvenating effect is mediated through the process of development and involves tissue stem cells, then its effect on the epigenetic age of the brain would appear to be modest, which indeed it does. It is to be noted, however, that improving brain function does not depend on neurogenesis as much as it does on synapse formation and factors such as NMDA receptors which decline in density with age.

Clinical suggestions are there for brain, heart, lung, and liver in that inflammation markers (IL-6 and TNF-α) went down and stayed down, and Nrf2 went up and stayed up. The rats became young and had the chemistry of the young, not just improved age markers! It is this that excites me so much!