Personal website: https://andrewtmckenzie.com/
Andy_McKenzie
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Why I’m not trying to freeze and revive a mouse
identity is irretrievably lost when the brain activity stops
My point here is that this is a very strong claim about neuroscience—that molecular structure doesn’t encode identity/memories.
How likely is brain preservation to work?
The examples you provided don’t actually support the “one funeral at a time” narrative in your title. Take Barbara McClintock’s jumping genes or Barry Marshall’s H. pylori discovery—in both cases, many scientists changed their views based on compelling evidence while very much alive. There are plenty of other examples of this. For example, the acceptance of prions as disease agents, the role of microbiomes in health, dark energy, and mitochondria’s bacterial origins all show how consensus can shift rapidly once a sufficient amount of evidence has accumulated. Scientists change their minds all. the. time.
This is not to say that there are not fads or incorrect beliefs in science—of course there are. And sometimes it can takes years or decades for them to be overwhelmed. But the “funeral” framing in particular is not only historically inaccurate but also promotes a harmful view that death is necessary for progress. What we actually see in these examples is that scientific views change when sufficient evidence accumulates and a sufficient number of people are convinced, regardless of generational turnover. Suggesting we need scientists to die rather than be convinced by evidence is both incorrect and ethically fraught. I am saddened to see it here and therefore strong downvoted this post.
Thanks for the clarification and your thoughts. In my view, the question is to what extent the polymer gel embedding is helpful from the perspective of maintaining morphomolecular structure, so that it is worth the trade-off of removing the lipids, which could potentially also have information content. https://brainpreservation.github.io/Biomolecules#how-lipid-biomolecules-in-cell-membranes-could-affect-ion-flow
You are in good company in thinking that clearing and embedding the tissue in a hydrogel is the best approach. Others with expertise in the area have suggested the same thing to me. I’m just not convinced, so I think that more research is required to tell whether that is the best approach.
ETA: Sorry, just saw your edit. Interesting thoughts on the interaction between preservation and reconstruction. Your perspective and goals make sense to me, although it is not exactly what we are pursuing at Oregon Brain Preservation. We are agnostic as to the potential method of revival and expect this to be relatively further away in the future, if it ever becomes possible.
Thanks for your interest!
Does OBP plan to eventually expand their services outside the USA?
In terms of our staff traveling to other locations to do the preservation procedure, unfortunately not in the immediate future. We don’t have the funding for this right now.
And how much would it cost if you didn’t subsidize it?
There are so many factors. It depends a lot on where in the world we are talking about. If we are talking about someone who legally dies locally in Salem, perhaps a minimal estimated budget would be (off the top of my head, unofficial, subject to change):
Labor cost of brain preservation = ~$500-1000
Cost of chemicals, disposable equipment = ~$100-300
Cost of death certificate, cremation, funeral services fees for the rest of the body = ~$1000-1500
Long-term preservation cost = very difficult to estimate, depends on economies of scale, and other factors, perhaps ~$1000-2000
These are rough estimates. But generally speaking, there is a reason that many brain banks around the world are also able to allow people to donate their brains for free. There are many many thousands of brains preserved in this way throughout the world. It is not nearly as expensive as traditional cryonics. Here is some more information about costs for similar type of procedure from the Brain Support Network: https://www.brainsupportnetwork.org/brain-donation/brain-donation-faq/
Cost is a common complaint about cryonics so I could see you becoming much bigger than the cryonics orgs, but judging by the website you look quite small. Do you know why that is?
I don’t know. A couple of guesses are that we are just getting started and not really doing any marketing because our focus is on researching the preservation methods. Also, it is likely that many people are skeptical of the preservation methods that we use, since they are new and different than others, as well as being experimental. Here is some more information about our research program, which you might find interesting: https://osf.io/preprints/osf/c28hm
We discuss the possibility of fluid preservation after tissue clearing in our article:
An alternative option is to perform tissue clearing prior to long-term preservation (118). This would remove the lipids in the brain, but offer several advantages, including repeated non-invasive imaging, and potentially reduced oxidative damage over time (119).
And also in our fluid preservation article we have a whole section on it. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11058410/#S7
I’m not sure why this option is much more robust that formaldehyde fixation alone. I haven’t seen any strong evidence for that. I do agree that it is potentially very useful for 3D reconstruction, but reconstruction is a much different problem than preservation.
I can’t speak for Adele, but here is one somewhat recent article by neuroscientists discussing memory storage mechanisms: https://bmcbiol.biomedcentral.com/articles/10.1186/s12915-016-0261-6
DNA is discussed as one possible storage mechanism in the context of epigenetic alterations to neurons. See the section by Andrii Rudenko and Li-Huei Tsai.
This is an important question. While I don’t have a full answer, my impression is that yes, it seems to preserve the important information present in DNA. More information here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11058410/#S4.4
Refactoring cryonics as structural brain preservation
Being against involuntary death and being open to change are compatible
Thanks for the comment. I’m definitely not assuming that p(success) would be a monocausal explanation. I’m mostly presenting this data to give evidence against that assumption, because people frequently make statements such as “of course almost nobody wants cryonics, they don’t expect it will work”.
I also agree that “is being revived good in expectation / good with what probability” is another common concern. Personally, I think niplav has some good analysis of net-negative revival scenarios: https://niplav.site/considerations_on_cryonics.html
Btw, according to the author, ‘Lena’ is largely a critique of exploitive capitalism: https://qntm.org/uploading
Cryonics p(success) estimates are only weakly associated with interest in pursuing cryonics in the LW 2023 Survey
Why wasn’t preservation with the goal of potential future revival started earlier in history?
Very high-effort, comprehensive post. Any interest in making some of your predictions into markets on Manifold or some other prediction market website? Might help get some quantifications.
A simple solution is to just make doctors/hospitals liable for harm which occurs under their watch, period. Do not give them an out involving performative tests which don’t actually reduce harm, or the like. If doctors/hospitals are just generally liable for harm, then they’re incentivized to actually reduce it.
Can you explain more what you actually mean by this? Do you mean if someone comes into the hospital and dies, the doctors are responsible, regardless of why they died? If you mean that we figure out whether the doctors are responsible for whether the patient died, then we get back to whether they have done everything to prevent it, and one of these things might be ordering lab tests to better figure out the diagnosis, and then it seems we’re back to the original problem i.e. the status quo. Just not understanding what you mean.
Out of curiosity, what makes you think that the initial freezing process causes too much information loss?
I agree with most of this post, but it doesn’t seem to address the possibility of whole brain emulation. However, many/(?most) would argue this is unlikely to play a major role because AGI will come first.
Thanks so much for putting this together Mati! If people are interested in cryonics/brain preservation and would like to learn about (my perspective on) the field from a research perspective, please feel free to reach out to me: https://andrewtmckenzie.com/
I also have some external links/essays available here: https://brainpreservation.github.io/
Thanks for writing this post. I completely agree that trying to fight involuntary death is a great idea.
A few thoughts:
In my view, recording an external mindfile (what I see/hear/say) is not nearly sufficient. Most of the information I value isn’t what I see, but how I react to it, such as the unique patterns of neural activation, the associations my brain makes, and the subtle emotional colorings. A video of me watching a game of bridge tells you nothing about why that particular card game reminded me of my grandparents, or how it shifted my mood in ways I couldn’t even articulate.
There’s a huge difference between recording outputs and preserving the computational substrate that generates those outputs. It’s like trying to recreate an AI model by saving only a relatively small amount of its chat logs. You’d be missing the actual architecture that makes it that particular system. (Now, if we could get enough behavioral data, maybe we could theoretically reverse-engineer the underlying computation. But we’re talking about orders of magnitude more data than what AR glasses and EEG caps will give us. You’d need the internal states, not just the outputs. In my view, your “portable advanced EEG” in the 2030s clearly won’t capture individual synaptic connection strengths or the molecular-level information that likely matters for long-term memories and personality.)
I would recommend reading or at least skimming the whole brain emulation roadmap, which you said you’re planning to do. It’s more about building an emulation on the basis of scanning a preserved brain.
For myself, I am focused on structural brain preservation, which I believe can address this problem well. I think we need to preserve the connectome and the physical instantiation of memory and personality, which could potentially allow for revival with the benefit of future technology. For a recent intro to this topic, see: https://www.frontiersin.org/journals/medical-technology/articles/10.3389/fmedt.2024.1400615/full
Please email me if you’re interested in discussing this more. Maybe I’m wrong about something—if so, I would love it if you could prove me wrong. I’m very glad you’re interested in this space!