The Clock Logic of Plasma Exchange

I begin from the paradigm that aging is not a random process but an adaptation, a programmed self-destruction. This was my entree into the field 27 years ago, and has been the theme of much of my research, including two books. For a summary of the evidence, here’s a blog post from 2015, and here’s the non-technical version of my book.

Once you accept that the body is killing itself on a schedule, you have to ask how the schedule is maintained. Just as growth is programmed in early life and then puberty is initiated by turning on sex hormones, aging happens when inflammation and auto-immunity and insulin resistance are gradually switched on when the body attains a certain age. This implies a master clock, probably the same clock that governs development also controls aging.

Where is that clock and how does it work? If we had an answer to these questions, we could reset the aging clock and an 80-year-old body would act like a 30-year-old body, with all the robust repair and regenerative mechanisms fully engaged.

The aging clock that we seek must have two conflicting properties. Of course, it must keep time reliably to trigger the phenotypes of growth, development, and then senescence on schedule. It must also be homeostatic. Homeostasis is a fundamental property of life. All biological systems tend to restore their state when deranged by the environment. If the clock is perturbed, it must be able to find its way back to a remembered biological age.

Homeostasis is a defining feature of living organisms, perhaps the most fundamental property of life itself. The word refers to the capacity of a system to maintain its state in the face of slings and arrows of outrageous fortune. For example, we can swim in ice water or we can trek through the Sahara and our bodies maintain a core temperature pretty close to 98.6ºF. We can drink Coca-Cola or we can fast for a week, and still the body keeps enough glucose in the blood to feed our cells without poisoning us with excessive blood sugar. We can take powerful proton pump inhibitors that jam with the body’s mechanism for creating stomach acid, but after a few months the body ramps up the acid factory as much as needed to digest our food.The point is that the body has many jobs that it needs to do, and it is exquisitely adapted to accomplish the most important of these no matter what are the outward circumstances. In the long run, the most important component of Darwinian fitness is the ability to keep on keeping on when the unexpected happens. Homeostasis.

But how can a clock be homeostatic? If the body’s clock is knocked far off the biologically-determined age, where is the reference information from which it can be reset?

The existence of a clock is implied by the paradigm in which aging is an adaptive program. The need for homeostasis is a general property of biological systems. The only way that the two conditions can be met simultaneously is if there are several independent time-keeping mechanisms, and they are constantly exchanging information. This condition derives from theoretical considerations. I concede that this is a dangerous way to draw conclusions about biology, which has always been primarily an experimental science. So I am going out on a limb to put forth this hypothesis: There ought to be several independent time-keeping mechanism in the bodies of complex organisms like the human animal, and there is continual cross-talk by which they are able to establish consensus, and reset the readout if one clock should differ substantially from the others.

I have written in this column about a central clock in the neuroendocrine center of the brain, the suprachiasmatic nucleus, as documented (independently) by Claudia Cavadas (Lisbon) and Dongshen Cai (NYC). Steve Horvath has convinced us that there is a decentralized clock in the epigenetic state of dispersed cells around the body. Perhaps this counts as more than one clock, since Horvath has measured differences in aging rates in different organs. Epigenetic changes in stem cells may deserve the status of a separate clock.Telomere length in stem cells may constitute another clock. The immune system appears to have its own aging schedule, which was the subject of Roy Walford’s first theory of aging. Perhaps oxidative status of the dispersed mitochondria constitutes a fifth clock. A new possibility is raised by the research from Michael Levin’s Tufts University laboratory. Levin has demonstrated a role for electrical patterns in morphogenesis, healing, and regeneration. His model for cancer is not genetic; rather he has demonstrate that he can create tumors from normal genomes by disrupting their electrical connection to one another, and he can cure cancer in highly-mutated tumors without killing the cells, merely by restoring the cells’ electrical connectivity. Levin has speculated that electrical patterning is lost with age because many vertebrates are able to regenerate limbs or parts of limbs early in life, and gradually lose this capacity as they mature.

We should not be surprised to discover other, independent timekeepers as well. After all, the body must be coerced into killing itself, despite robust Darwinian adaptations that support individual survival and fecundity. If there were an easy path to mutating aging out of existence, then natural selection operating on a short time frame would have found it (with disastrous consequences for the species and the ecosystem).

If my hypothesis is correct, then all these clocks are exchanging signals, cross-checking to establish a consensus age and resetting accordingly. How do the various clocks exchange information? The obvious place to look is signal molecules in the blood. These may be hormones or other large proteins; they may be short peptides; they may be RNAs or ribozymes; they may be extracellular vesicles containing a package of coordinated signal molecules of various types. Age signaling may be accomplished with a combination of all the above. This reasoning leads to the inference that exchanging young blood plasma for old ought to be a robust anti-aging strategy. Besides erythrocytes and leukocytes, the blood carries many thousands of different signals as dilute molecular species dissolved in plasma. Some of these, I suggest, constitute primary information about the age state of the body. This information must be capable of resetting all the body’s different aging clocks.

Of course, the work has commenced nearly two decades ago. Experiments in heterochronic parabiosis. Irina and Mike Conboy did the first experiments in the modern era while they were graduate students at Stanford. Harold Katcher wrote up theory of why this work ought to be the portal to robust rejuvenation. The Conboys have gone on to promote a perspective in which old age is established affirmatively by molecular species in the blood of old animals. In their model, diluting old blood with neutral saline albumen is a path to rejuvenation. In cooperation with Dobri Kiprov, they have initiated a human trial in rejuvenation based on blood dilution.

Katcher and Tony Wyss-Coray and Amy Wagers have championed the converse perspective, that senescence is linked to a dearth of youthful signals in the blood of older animals. Katcher has done proof-of-concept experiments in rats. Wyss-Coray has built a company based on injecting blood factors to treat Alzheimer’s Disease. The company, called Alkahest, has been acquired by the Spanish giant, Grifols, which has been a major player in plasmapheresis therapies. Dan Stickler has a clinic in Texas offering blood plasma from young donors. David Haase at the Maxwell Center has long experience offering plasmapheresis as a therapy.

I think it likely that the most effective strategies for rejuvenation will involve both removal of pro-aging factors and addition of anti-aging factors to the blood plasma. Discovering what these factors are and how they work ought to be a major target for research in the field of medical gerontology. One easy place to start is with extracellular vesicles. These are larger than molecules, smaller than cells, and they are normally filtered out in plasmapheresis. But they may play a crucial role in plasma exchange as an anti-aging strategy; it will be important to know.

Reality check

How well can we expect the new plasma transfusion therapies to work? We have some experience that should guide our expectations.

Two summers ago, I was hit by a car while riding my bicycle and lost most of the blood in my body. Heroic surgery kept me from bleeding to death, against all odds. I received blood during that first surgery and more blood was lost and replenished during 7 follow-up surgeries. The median age of blood donors in America is about 47. I was 72. It’s possible that replacement of the majority of my blood with younger donors had a rejuvenating effect, but if there was any benefit at all, it was not dramatic enough to be noticeable to me or my family.

5 million people a year receive blood transfusions. Some of them are very old, and none of them has skipped out of the transfusion clinic with youthful hair color and de-wrinkled foreheads.

A history of blood donation year after year has a substantial benefit for life extension, but it is not dramatic. Giving a pint of blood is equivalent to a 10% dilution, and habitual donors do this a few times per year. (I was donating blood several times a year before my 2021 hospitalization.) Based on standard life tables, 30% decrease in mortality is equivalent to about 3 years of added life.

From this, I would expect that my proposed homeostatic age-resetting mechanism works slowly. We don’t know specifically the lifetime of aging signals in the blood because we don’t know what these signals are; but studies of generic protein turnover in blood plasma suggest ten days or so as a reasonable guess. In Katcher’s rats, the figure is closer to 2 days.

From this, we can say it is likely that resetting the rat’s biological clock takes at least several times 2 days, and resetting the human clock requires at least several times 10 days. It may require repeated transfusions every 10 days over a period of months to see the full effect.

Concerning the effectiveness of E5 in Katcher’s rats, we are still learning. The biomarkers, including Horvath age, were very promising. Longevity seemed to be increased only modestly, however — except for Sima, the last remaining rat (out of 8) who has now broken records for rat longevity at 46 months. Harold’s reported rejuvenation of skin on one hand based on a single application of E5 is an intriguing anecdote that encourages us to hope for the best.

I’m going to pose a much more speculative argument that rejuvenation through transfusions of young blood will be effective, but will not change paradigms about human lifespan. I conjecture that the richest and most powerful people in the world have special access to technologies that are unavailable to you and me. Have some of them been getting blood transfusions from young donors? David Rockefeller died six years ago, just short of 102 years old. Queen Elizabeth died at 96. Evelyin de Rothschild died last year at 91. Henry Kissinger is still alive at 99. Jimmy Carter is 98. George Soros and Warren Buffett are each 92 and they look it.

The bottom line

I remain optimistic about Harold Katcher’s work and about plasma exchange in general, but we still have a lot of work to do.

And by the way

There are other ways to die, unrelated to age. Bioweapons research has spawned a worldwide epidemic, killing millions, and next time could be worse. We live in a time when collective threats to our existence may soon become as great as the mortality burden imposed by age.

Aging evolved for the purpose of stabilizing ecosystems. Human beings have shown themselves to be adept at destabilizing ecosystems, and now we want to further expand our numbers and extend our power of nature. Mankind cannot “transcend” nature. Humans cannot live outside the context of Gaia’s ecosystem. If we try, it will be the extinction not of Gaia but of the human race.

I believe that the pursuit of longevity is not only scientifically feasible but also worthwhile. But this grand project must be pursued in tandem with an even grander project, which is to change our relationship to naturally ecology from a miner and exploiter to a cooperative steward.

There is evidence that the native population of America had such an ethos, together with the wisdom and the science to create richer ecosystems for their own sake and for the sake of nature’s abundance and diversity. It is required of humanity that we quickly learn that lost art, on pain of extinction.

31 thoughts on “The Clock Logic of Plasma Exchange

  1. Excellent essay, thank you, Josh. At least we know that blood donation has the benefits of preventing the accumulation of toxic levels of iron as well as significantly reducing levels of toxic PFAS.

  2. Josh, brilliant post. Agree with every line in that post. From what I have learnt you did seem to have a remarkable recovery and that can not happen on its own at 72 after such a horrendous accident. The younger blood may have helped and any other supplement you might have taken. You may already have been much younger biologically then 72 to have survived this near fatal event. Michael Levin’s work tells us how incredibly complex our biology is and just when we think we have a better understanding of it a whole new paradigm opens up.

  3. Having self tested old plasma dilution/removal myself the best way I could without having to go to one of those clinics I am convinced getting rid of the old stuff periodically will benefit your health span but is not some mini-miracle when it comes to that. At 53 years old I did 8 plasma donations over about a 3 and a half week span which should have removed roughly 88% of the old plasma over that time. The benefits after about 2 weeks of feeling weak from the low albumin levels were that I felt like a little fog had been lifted (similar to a whole blood donation but a little different feel to it). For about the next 2 months it felt like my body was working on itself a little more than before and my skin improved some appearing to have more collagen in my facial skin. I felt a little stronger with more pep and the inflammation in my elbow disappeared. The different feeling seemed to level off after about 2 months or so.

    My guess is dilution clearly helps once you reach your 50s and above but concentrated proteins etc. from young plasma will end up being a much bigger game changer for health span than dilution on its own. I think on a few things it probably takes a good amount of the young factors (probably more than simply replacing 1-1 old plasma to young plasma) to overcome some of the down regulation of things that occur when we get old. I am assuming that these E5 tests are giving a concentrated amount of the young factors (even more than a young person might have naturally) but I am not 100% sure on that.

  4. Josh is at the foot of the mountain of longevity. It is necessary to move to higher levels of the hierarchy of ideas about a person. High levels of longevity are associated with the structure of a person, and a person is a biological body and Soul, which is an information structure. A man is a Soul, and a man has a biological body only on Earth, and then after death he has only a Soul and its mental and ethereal bodies. The soul, not the brain, processes all the information. The control programs of the Soul are tuned to the aging process. However, you can switch the aging process to rejuvenation. I found such a switch – this is a change in the magnetic field strength of hydrogen atoms in the nerve cells of our body. At a certain strength of the magnetic field of the hydrogen atoms of the nerve cells of our body, aging switches to rejuvenation. Dozens of people rejuvenate their body. Rejuvenation goes up to 16 years of age and then stops. The first girl from the Dnieper in one year reduced her biological age from 23 to 16 years. The speed of rejuvenation is on – for 45 days of rejuvenation, the biological age decreases by 1 biological year. Switching the aging process to rejuvenation is carried out by taking information (in a word) activated malic acid, which has a magnetic field strength of hydrogen atoms of 222 222 A/m. You can all repeat such experiences. Information activation is carried out by me on a photo of malic acid, or on a photo of a person, or on a photo of water. The process of rejuvenation has already begun for people aged 20 to 80 years. The older the age, the longer the rejuvenation process takes.

    • Excellent information and exciting news all coming in from Spectrum Plasma who is harvesting young Fresh Frozen Plasma (yFFP) right here in Texas. The therapeutic uses are endless.

  5. In the Conboys’ plasma dilution experiment, 50% of the plasma was replaced at one time. It seems possible that this engendered a reset of the system that diluting only 10% at a time may not.

    Also, I’ve suggested that iron is one the removed factors causing aging (broken record, I know), but there’s also the possibility that lower blood viscosity plays a role. This promotes better circulation as well as an increase in insulin sensitivity.

  6. Deciphering the complexity of human biology to discover both pro- and anti-aging factors is indeed fascinating knowing that (1) we now know that a signal exists in a biological matrix as accessible as blood, and (2) we have all the technical tools to discover that signal, as complex as it can be. In other words, we just have to setup the right study. Which, in my opinion, should be systems biology omics applied to blood samples collected on >1M subjects with results mapped to basic health information. Much more accessible than say the human mission to Mars. Exciting times.

    • I am a big fan of Peter Fedichev and has just talked about what you have described. Get methylation age of a bunch of old people. Identify the slowest and fastest agers, do blood protein analysis to compare, find existing meds that target the genes that make those proteins.

      • That study that showed people had three stages (approximate ages) of life where the proteome changed a lot would be a good start trying to identify certain things that could be manipulated to extend healthspan and maybe lifespan. The only problem with it was when they narrowed it down to the proteins and levels of them they could use to actually predict someone’s age pretty accurately almost 2/3 of them were not predictive for both sexes but maybe the ones that were do hold some big possibilities.

  7. More recent papers have pointed to aging being long genes not working as a consequence of a shortage of Acetyl-CoA.

    c2022/12/its-long-genes-that-stop-working.html

    Transfusing blood helps in reducing IL-10. There also need to be questions as to what has been added to transfused blood that might help,

  8. What about non-blood based signaling; paracrine, juxtacrine, autocrine? Could signaling happen via other bodily fluids; lymph, cerebrospinal fluid? Hard enough just figuring out the blood. I hope we don’t need to address these things as well.

  9. Sure, ten days is a reasonable guess at the lifetime of signal molecules in the blood. But generic protein turnover isn’t much to go on. How do we get a figure of two days for rats? (I couldn’t access the linked article. And what I could access didn’t seem to address the matter.) Why should we think the figure for humans is 5 times longer? Aren’t we talking about molecules that are highly conserved across taxa? More importantly, how meaningful is the average lifespan of said molecules? Perhaps some of the key players have much shorter lifespans. Maybe one would need a transfusion every hour for a few months, or some other daunting, inconvenient number. Here’s what I daydream about (lol): A diabetic friend of mine has a tiny gizmo affixed to his abdomen that measures his blood sugar constantly. Maybe we need hardware like that, but instead of monitoring glucose levels, it destroys pro-aging signal molecules, and generates youthful signals 24/7. How? I don’t know. Aptamers to bind the former? Bacteria, sessile to the device, that generate the latter as part of their genetically engineered metabolism? Such is my fantasy life. 🙂

  10. This process of establishing a “consensus age” – I wonder how that plays out. I wouldn’t expect some democratic “one molecule, one vote” method. “Consensus” suggests (eventual) unanimity. The prospect of having to youth-ize every voice in the body is daunting. Hopefully any signals we fail to address can be made to toe the line by those we do. I find reason for optimism here. If there were signals with out-sized voices, wouldn’t we see instances of premature aging in the form of people (and animals) with unfortunate mutations affecting such? I’m not sure we do. There are cases of people getting cancer at young ages, early-onset Alzheimer’s and what not, but such strikes me as distinct from aging. Those folks don’t exhibit other hallmarks of aging; gray hair and the like. I’m not inclined to interpret cases like that as a strong aging signal getting its way. One might mention progeroid syndromes, but I suspect that merely looks like aging, and aren’t they quite rare?

      • I think the biggest problem that he (Greg Fahy) has is that if it pans out big pharma wouldn’t be interested because it doesn’t have a patentable drug involved. I mean a cocktail of DHEA, metformin and growth hormone all drugs that are already available, Not much money for big pharma in pushing that, screw what is in the public’s (our) best interest.

        • What do we need big pharma for? Is Greg languishing for lack of research funding? The big picture is obvious to me – that if we had a different, big pharma-less economic system we’d probably have a cure for aging already. But as far as Fahy’s work in particular – if he’s discovered something, just employ it. If the drugs are already available, so much the better. We don’t have to synthesize them. Friendly doctors willing to prescribe off-label can’t be that hard to find.

          • https://theprint.in/health/research-hypertension-drugs-could-be-repurposed-to-delay-ageing/1332220/

            Speaking of off label use this hypertension medication worked about as good as rapamycin in early trials. There is a longer version I can’t find now that says the effect was the same whether treated with this or rapamycin and that combining both didn’t increase the effect from either. It sounds like the chances of side affects are lower with this than rapamycin though.

          • He (Fahy) probably does need allot more funding/publicity; His original TRIIM-X trial only had about 9 participants. His follow up currently running has more around ~50 or so participants not really a very large study. And not very much attention from the academic community, big pharma (of course), and/or the new media.

        • It might be worth noting that Greg Fahy addressed this. He has a way of producing HGH (the expensive part) more cheaply, so he thinks that he can get some funding by doing that. Of course, that’s more more thing that has to go right than with most drugs, but it does look like a plan that could work. He has also discussed that certain expensive conditions that Medicare covers might be better treated, and more cheaply by using his protocol.

  11. Brilliant! You have collected and expressed all that was on the tip of my tongue – and more – in a way that is perfectly understandable.

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