[Paleopsych] The 25-Year Wait for Immortality
Christian Rauh
christian.rauh at uconn.edu
Thu Apr 14 15:48:24 UTC 2005
Will the rich be the ones to benefit from this technology?
Will it be withheld from others? Patented?
Would there be a clash between mortals vs. immortals?
Should immortality be a universal right?
Will immortals ever risk their lives for anything?
Would life become too valuable to sacrifice for an idea?
Christian
Steve Hovland wrote:
> Hang in There: The 25-Year Wait for Immortality
> By Ker Than
> Special to LiveScience
> posted: 11 April 2005
> 06:32 am ET
>
>
>
> "I think it's reasonable to suppose that one could oscillate between being
> biologically 20 and biologically 25 indefinitely."
> -- Aubrey de Grey
>
> Time may indeed be on your side. If you can just last another quarter
> century.
>
> By then, people will start lives that could last 1,000 years or more. Our
> human genomes will be modified to include the genetic material of
> microorganisms that live in the soil, enabling us to break down the junk
> proteins that our cells amass over time and which they can't digest on
> their own. People will have the option of looking and feeling the way they
> did at 20 for the rest of their lives, or opt for an older look if they get
> bored. Of course, everyone will be required to go in for age rejuvenation
> therapy once every decade or so, but that will be a small price to pay for
> near-immortality.
>
> This may sound like science fiction, but Aubrey de Grey thinks this could
> be our reality in as little as 25 years. Other scientists caution that it
> is far from clear whether and for how long science can stall the
> inevitable.
>
> De Grey, a Cambridge University researcher, heads the Strategies for
> Engineered Negligible Senescence (SENS) project, in which he has defined
> seven causes of aging, all of which he thinks can be dealt with.
> (Senescence is scientific jargon for aging.)
>
> De Grey also runs the Methuselah Mouse prize for breakthroughs in extended
> aging in mice. The purse of the M Prize, as it is called, recently grew
> beyond $1 million.
>
> LiveScience recently spoke with de Gray about his idea of living longer,
> and perhaps forever.
>
>
> ------------------------------------------------------------------------
> --------
>
>
> LiveScience: What is your definition of aging?
>
>
> Life Expectancy in America Hits Record High
>
> Infusion of Young Blood Revives Old Muscles
>
> Roots of Graying Hair Discovered
>
> Ray Kurzweil Aims to Live Forever
>
>
>
>
> Aubrey de Grey: The definition that I like is not very good if you want to
> cover all species, but it's pretty good if you want to do something about
> it. I define aging as the set of accumulated side effects from metabolism
> that eventually kills us.
>
> Is your goal to just extend the human lifespan substantially or to enable
> us to live forever?
>
> I don't see any inherent limit to how long it would be desirable to live.
> If life is fun at the moment, because one is healthy and youthful, both
> mentally and physically, then one is not likely to want to die in the next
> year or two. And if a year or two down the road, life is still fun because
> one is still youthful and so on, then the same will apply, and I can't see
> a time when that would cease to be true.
>
> When did you first come up with idea for your SENS project?
>
> Well, I've always considered aging to be undesirable, but I didn't begin to
> consider that I could make a contribution until about ten years ago. I
> suppose the major breakthrough was when I came up with the scheme that I
> now describe as SENS, and that happened about four years ago.
>
> 7 Deadly SENS
> Nuclear Mutations/Epimutations
> These are changes to the DNA, the molecule that contains our genetic
> information, or to proteins which bind to the DNA. Certain mutations can
> lead to cancer.
>
> Mitochondrial Mutations
> Mitochondria are components in our cells that are important for energy
> production. They contain their own genetic material, and mutations to their
> DNA can affect a cell's ability to function properly.
>
> Intracellular Junk
> Our cells are constantly breaking down proteins that are no longer useful
> or which can be harmful. Those proteins which can't be digested simply
> accumulate as junk inside our cells.
>
> Extracellular Junk
> Harmful junk protein can also accumulate outside of our cells. The amyloid
> plaque seen in the brains of Alzheimer's patients is one example.
>
> Cell Loss
> Some of the cells in our bodies cannot be replaced, or can only be replaced
> very slowly.
>
> Cell Senescence
> This is a phenomenon where the cells are no longer able to divide. They may
> also do other things that they're not supposed to, like secreting proteins
> that could be harmful.
>
> Extracellular Crosslinks:
> Cells are held together by special linking proteins. When too many
> cross-links form between cells in a tissue, the tissue can lose its
> elasticity and cause problems.
>
>
>
>
> What happened was that I was gradually learning a lot of biology because my
> wife is a biologist. I was originally trained as a computer scientist, and
> I regarded aging as obviously undesirable but not my problem, that someone
> else would be working on it.
>
> But the more biology I learned, the more I also learned about biologist and
> about the attitudes toward working on the biology of aging that biologists
> tended to have, and basically, I wasn't very impressed. I found that rather
> few biologists were interested in the problem at all, and I thought, "Well,
> that isn't very good,", so I thought I'd see what I could do.
>
> Your background is in computer science. How does that qualify you to
> spearhead a project on aging?
>
> My background is enormously beneficial. There are really very important
> differences between the type of creativity involved in being a basic
> scientist and being an engineer. It means that I'm able to think in very
> different ways and come up with approaches to things that are different
> from the way a basic scientist might think.
>
> Could you give me an example of when your background has proven useful?
>
> Well, I suppose that the whole SENS project is one big example. What I've
> done there is I've identified a set of things to fix, a set of aspects of
> aging that we have some respectable chance to repair, and I've realized
> that if we can do all of these things reasonably well, then we're done.
>
> Basically, we'll have made the age related problems that we suffer from
> these days no longer an inevitable consequence of being alive. What I've
> done is basically factored out all the complicated details of how
> metabolism causes these things in the first place. It will be many decades
> before we understand the way cells and organs work well enough to be able
> to describe in detail the mechanism of how these problems actually occur.
>
> But my way of thinking is that we don't need to know the details of how
> they happen. So long as we know what these things are that do happen, we
> can figure out ways to fix them. This is counter to the ways that
> scientists think, because scientists are interested in knowledge for its
> own sake, whereas I'm interested in knowledge as a means to an end.
>
> Could you give me a timeline for how you envision your project succeeding?
>
> The first part of the project is to get really impressive results in mice.
> The reason that's important is because mice are sufficiently furry and
> people can identify with them. If we get really impressive results in mice,
> then people will believe that it's possible to do it in humans, whereas if
> you double the lifespan of a fruit fly, people aren't going to be terribly
> interested.
>
> Now, what I want to do in mice is not only develop interventions which
> extend their healthy lifespan by a substantial amount, but moreover, to do
> so when the mouse is already in middle age. This is very important, because
> if you do things to the mouse's genes before the mouse is even conceived,
> then people who are alive can't really identify with that.
>
> I reckon it will be about 10 years before we can achieve the degree of life
> extension with late onset interventions that will be necessary to prove to
> society's satisfaction that this is feasible. It could be longer, but I
> think that so long as the funding is there, then it should be about 10
> years.
>
> Step two will involve translating that technology to humans. And because
> that's further in the future, it's much more speculative about how long
> that's going to take. But I think we have a fifty-fifty chance of doing it
> within about 15 years from the point where we get results with the mice. So
> 25 years from now.
>
> What do you think about the idea that with so much life at stake, people
> would be less willing to take risks?
>
>
> The journal of the SENS institute.
>
>
>
>
> I used to be more pessimistic about this than I am now. Five or six years
> ago I wrote a book in which I predicted that driving would be outlawed
> because it would be too dangerous to other people, but now I think that
> what's actually going to happen is that we'll just throw money at the
> problem. Rather than simply avoiding activities that are risky, we'll make
> them less risky through technology. For example, it's perfectly possible
> already to build cars that are much safer than those which most people
> currently drive, and it's also possible to build cars that are safer for
> pedestrians-with auto sensors and auto braking to stop from hitting a kid
> running out in the road and things like that.
>
> It's just a matter of priorities. When there isn't that many years of life
> to lose, the priority isn't there to spend the money. It's all a matter of
> weighing out the probabilities.
>
> Once the technology is available, nearly everyone is going to want it. Of
> course, there's going to be a minority of people who think it's better to
> live more naturally in some way or other. We have parallels like that in
> society today, like the Amish for example.
>
> Some would say that death is a part of life. What would be your response to
> those people?
>
> Death will still be a part of life when we haven't got aging anymore. If
> you mean that some people would say that aging is a part of life-well,
> that's certainly true, but a couple hundred years ago tuberculosis was a
> part of life, and we didn't have much hesitation in making that no longer a
> part of life when we found out how.
>
> What do you say to critics who think that this money could be better spent
> towards curing diseases like cancer?
>
> This is a very important point. Because we're going be in a situation where
> we can extend lifespans indefinitely, this argument doesn't work. If it
> were a case of simply having a prospect of extending our healthy lives by
> 20 or 30 years, then one could legitimately argue that this would be money
> more ethically spent on extending the lifespan of people who have a below
> average lifespan. But when we're talking about extending lifespans
> indefinitely, I don't think that really works. The other thing to bear in
> mind, is that it's not an either or thing. The reasons why people in Africa
> for example, have a low life expectancy is not just because of medical
> care, but also because of political problems.
>
> What kind of life will the immortal or nearly-immortal lead? Will they have
> to be on a special diet, or have constant organ transplants?
>
> Like any technology, when it first starts off, it will be a bit shaky, a
> bit risky, it will be very laborious and expensive and so on, but there
> will be enormous market pressures that will result in progressive
> refinement and improvement to the technology so that it not only becomes
> more effective, it becomes more convenient and so on. This will be an
> example of that.
>
> In a very general sort of sense, one could probably think in terms of
> having to go in for a refresh every 10 years or so. Exactly what would be
> involved in that will change over the years. It might start off as lets say
> a month in the hospital, and 10 years down the road, that will turn into a
> day in the hospital.
>
> A good parallel is vaccines. For example, when we take a holiday in Africa
> or Southeast Asia or whatever, we get a shot to make sure that we don't get
> malaria. And that's all we have to do, and when we get there we can eat Mc
> Donald's as much as one likes.
>
>
> Aubrey de Grey
>
>
>
>
> So you think it'll one day be as easy as getting a vaccine?
>
> Yes, that's right. A lot of these things, even in the early stages will
> amount to vaccines and drugs. Though of course, there will also be a lot of
> gene therapy and stem cell therapy and much more high tech stuff.
>
> Why did you establish both an institute and a prize?
>
> I think it's very important to have this two-prong approach. The idea here
> is that we don't really know what's going to work, but we have a fair idea
> of approaches that have a good probability of working.
>
> If you look at past technological achievements, some of them succeeded by
> just throwing serious effort and serious resources at the problem, and
> people were pretty sure of what they had to do to make the thing work. The
> Manhattan Project is a fine example of that. Everyone basically knew how to
> build the atomic bomb, it was just a question of working out the kinks.
>
> Then we've got things where there were loads of different possibilities
> about how the thing might be done, and it was important to motivate people
> and give incentives. For example, when Lindbergh flew across the Atlantic,
> that won a prize. And when someone invented a chronometer that worked
> properly at sea, that won a prize. Things like that. That was where you
> wanted to give incentives for people to follow their hunches, because it
> wasn't very clear which approach was going to work.
>
> I think that when we're talking about life extension, we're sort of halfway
> between these two situations. We have a bunch of ideas which one can make a
> good case that it's going to work, but we also want to hedge our bets, and
> let people follow their hunches as well.
>
> Of your seven SENS targets, which do you consider to be the most important?
>
> It's not possible to say. I don't think we will be able to achieve more
> than a relatively modest amount of life extension, if any, until we can get
> at least five or so of these things working, and we might need to do all
> seven before we get more than a decade of life extension.
>
> Why do you personally want to live forever?
>
> It's not really a matter of living forever, it's just a matter of not
> wanting to die. One doesn't live forever all in one go, one lives forever
> one year at a time. It's just a case of "Well, life seems to be fun, and I
> don't see any prospect of it ceasing to be fun unless I get frail and
> miserable and start declining." So if I can avoid declining, I'll stay with
> it really.
>
> What would you do if you could live substantially longer?
>
> They say variety is the spice of life, so I don't think I would do the same
> things every day. I'd like to be able to spend more time reading, and
> listen to music, and all that sort of thing, things that I never get to do
> at all at the moment.
>
> You think this project is going to succeed in your lifetime?
>
> I think it's got a respectable chance. I'm definitely not relying on it. My
> main motivation comes from the thought of how many lives will be saved.
>
> Your strategy would involve not only preventing aging, but reversing it as
> well. Does that mean people will get to choose what age they want to
> remain?
>
> Absolutely. So the idea is that we wouldn't be eliminating aging from the
> body. It'll be a case of going in periodically and having the accumulated
> damage repaired. So exactly what biological age you actually have at any
> point is really just a question of how often you go in for rejuvenations
> and how thorough they are.
>
> So the more treatments you undergo, the younger you can be?
>
> That's right. I think it's reasonable to suppose that one could oscillate
> between being biologically 20 and biologically 25 indefinitely.
>
>
>
>
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