[extropy-chat] Cryonics without comprehensive brain disassembly? - No
Robert J. Bradbury
bradbury at aeiveos.com
Tue Apr 20 17:06:12 UTC 2004
On Tue, 20 Apr 2004, Brett Paatsch wrote:
> No you don't *have* to show me or anybody anything. BTW your
> citations [1, 2, 3 etc don't map to anything.]
How annoying (editing error). Let me try again (see the end of the msg).
> So it's trivial then. All we need is nanosantas :-)
Not completely true -- one does probably need at least
highly parallel AFMs/STMs -- or alternatively very clever
bioengineered cells that are very good at the repair of
tissue that has been damaged (engineered stem cells for
example).
> I'd noted that a lot of the keenest advocates of molecular manufacturing
> seem to be pretty keen on cryonics as well. Perhaps a cynic might
> see a link there ;-).
Of course. People supporting cryonics presumably have to have
some optimism that the problems will be solved in one way or
another. MM is a relatively well defined path by which one might
build the necessary technical components to solve the problems
involved in cryonics.
Re: other technologies
> I can't imagine why that's so hard :-)
People are working on alternate technologies all the time.
Survival of ischemia-reperfusion injury is a classic example.
> I guess it hard to provide more details then the "humpty dumpty" stuff
> because you are time constrained. Aren't we all.
Fractured samples of solid objects have a reasonably unique 3D
structure. That is why I can take 2 pieces of fractured diamond
and precisely put them back together (mind you one would need something
relatively complex to rejoin covalent bonds that have been broken) --
but reassembly of fractured biological tissue is much simpler because
most, if not all, of the bonds that will be broken will be hydrogen
bonds and these will naturally self-assemble themselves.
> Then I'm not a liberty to be persuaded by it. And more to the point
> it can't persuade others that don't see it either. I'm only one person
> and I don't even vote in the US.
(I'll ask Robert F. if it is ok to release the paper.)
> > I am extending the idea that if many types of cells can be frozen
> > and reanimated and function properly that the cells of the brain
> > can be as well. Eugen or Anders might know if people have
> > actually frozen and reanimated neurons.
>
> By Eugen and Anders didn't tell me seek to correct the
> misperception - indicated either - you did. Its your perception
> that you work from isn't it?
I'm not sure I understand this question. E/A may simply be more
familiar with whether or not neurons or brain tissue have been
frozen and thawed and returned to am operational state.
> This is a country mile from refuting my assertion.
Ok, since this has been a long thread -- why don't you restate
your assertion(s)?
Mine would be:
1) It is probably possible to repair the brain using the original
atoms and structure after it has been frozen (this is in part
the subject of [1]).
2) It is probably possible to completely disassemble a brain to
an atomic level and reassemble it if one has advanced MNT capabilities.
3) It is probably possible to completely disassemble a brain, map
out its neural architecture and reassemble it on completely
different hardware (e.g. uploading).
Robert
1. http://www.merkle.com/cryo/techFeas.html
2. R. A. Freitas, "Implications of Natural Internal Radiation
(Endoradiation) for the Reanimation of Cryonics Patients"
(1999)
3. Pakkenberg, B. & Gundersen, H. J. G., "Neocortical Neuron
Number in Humans: Effect of Sex and Age", J. of Comparative
Neurology 384:312-320 (1997)
More information about the extropy-chat
mailing list