X-Message-Number: 3208 From: Brian Wowk <> Date: Tue, 4 Oct 94 16:15:59 CDT Subject: SCI.CRYONICS.Fixation,etc. Ian Taylor: >Recently Steve Bridge wrote: >>My personal, non-official guess, is that within 50 years it will be >>possible for a living, healthy human being to be placed in some form of >>very-long term (if not technically "permanent") biostasis and be revived >>with no ill effects. >Thanks for for non-official guess Steve ;) and for such a unexpectedly >full response. With all respect Steve your answer was not to the question I >was trying to ask. Let me clarify. My question is far less demanding on our >technology. I am not requiring initially a reversible process; only damage- >free entry into biostasis, the critical first step as I see it. We then rely >on future technology to restore function etc. To me this is *the* question: >how far away is our current technology from an ideal biostasis technique. I realize your questions are directed at Steve Bridge, but I thought I'd take a stab at them anyway. I agree completely with Steve's estimate of 50 years as the likely timeline for achieving demonstrably reversible suspended animation, and I suspect we agree on most other issues here as well. You ask about achieving "damage-free" entry into biostasis. This is a bit of an oxymoron because human beings (as currently designed) with stopped metabolism are inherently damaged, and have no way of spontaneously regaining function. I assume you are really asking when will we have a technique that we are certain is reversible with future technology. The answer is that we really won't know for *certain* until we can actually revive the person. The above point is very relevant to your questions about fixation. There are some good arguments in favor of supplementing freezing or vitrification with chemical fixation. The problem with fixation is the lack of feedback. Frozen or vitrified cells will often spontaneously recover function after rewarming. The extent of functional recovery is a direct measure of the success of your preservation procedure. In fact, we are probably less than 5 years and a million dollars or so away from achieving full functional recovery of *entire brains* from -130'C using vitrification only. What happens now if you chemically fix? Well, you lose all possibility of using function to measure preservation integrity, and virtually guarantee that your patient will need full-blown nanotechnology for recovery. This is why fixation is not used in cryonics. It's too risky, with too little feedback. > A table like this would help me to understand the current > state of practice, perhaps you can correct and complete it: > Biostasis Damage due Duration of > Technique to technique Biostasis Notes > Cremation 100% N/A For completeness ;) > Burial 99% 100 years? Bones, DNA only ... ? > Dry Ice 5%? 1 year? Old technique > Vitrification 1%? Indefinite? Current technique? > Fixation & Vit. 0.1%? " Proposed " > Ideal 0% Indefinite Complete preservation >WARNING the above table is for discussion purposes only, and >most likely has no resemblance to fact. Damage mechanisms in any of the above procedures are multi-dimensional and cannot be characterized by a single number. Cryoprotected (glycerolized) freezing is the current state of the art in cryonics. Resulting damage includes cell dehydration, disruption of cell-to-cell relationships, torn membranes, protein denaturation and possibly macroscopic fractures. The literature and sign-up paperwork of Alcor and CryoCare contain extensive discussions of these effects. Most of these problems go away if vitrification is used instead of freezing. However vitrification is at least a decade away from practical implementation, and even then will only be used on a single organ (the brain). Thank you for your interest. --- Brian Wowk Patient Care Director CryoCare Foundation Rate This Message: http://www.cryonet.org/cgi-bin/rate.cgi?msg=3208