X-Message-Number: 5376 From: Date: Fri, 8 Dec 1995 13:41:14 -0500 Subject: suspended animation Interesting that some talk about broadly-defined suspended animation should appear today. Yesterday a man named Karl Schreier (an Alcor member) visited Alcor and also visited me, and talked with Hugh Hixon and with me about some of his research ideas. He has some background in biology, although not a doctorate, and his livelihood is in the business world. One of his ideas is that there should be a research focus on suspended animation in the range roughly - 2.5 C to 10 C. This would involve what he calls "assisted low temperature homeostasis." From perhaps 10 to 30 metabolites would be monitored and, where necessary, corrected or supplemented. Because of the reduced rate of metabolism and other processes, and because the patient or experimental subject is still autonomously maintaining most of its homeostatic functions, he thinks such a patient might be maintained for considerable periods. If the period were very long (highly unlikely, I'd say) we would have an alternative (probably very expensive) to cryostasis; in any event there would be obvious and significant implications for clinical medicine and transplant surgery. He estimates a cost of $50,000 for equipment and $20-30,000/year for the work. (He is also interested in getting Ukrainians to do research, but warns that most former Soviets have been taught to lie, cheat, and steal in order to survive and must be approached with extreme distrust; I told him I was convinced that did not apply at all to Dr. Pichugin.) I suggested that he run his ideas past BioTime and BioPreservation and Greg Fahy. (He is attending the upcoming A4M meeting in Las Vegas.) No doubt he would like any other input also. Fax (315) 265-0471. My own reaction is one of skepticism, as I told him; I can think of countless potential obstacles or serious difficulties, especially as regards long term suspended animation by such methods. But with respect to clinical medicine applications the story may just possibly be different and more positive. That would also be gratifying. Mr. Schreier, naturally, would like to get some credit for his ideas if they pan out, but in any event would like to see them pursued. How does his approach differ from the old work of Klebanoff and others with dogs, and the more recent work of BioPreservation with dogs and of BioTime with hamsters and primates at near-freezing temperatures? Presumably in the details, including the number and character of the metabolites monitored and controlled, and the manner of doing it. How much he has to contribute here remains to be seen. Robert Ettinger Rate This Message: http://www.cryonet.org/cgi-bin/rate.cgi?msg=5376