Salamander

  • 100 Posts
  • 219 Comments
Joined 3 years ago
cake
Cake day: December 19th, 2021

help-circle



  • Thanks a lot for looking into this!

    While the iPSC technology has not yet advanced to a stage where therapeutic transplants have been deemed safe, iPSCs are readily being used in personalized drug discovery efforts and understanding the patient-specific basis of disease.

    I am not super familiar with the topic, but I have been told of some successful animal studies on implanting the organoid tissue into the animals from which the stem cells were derived.

    This other article from 2013 lists a few concerns, and I think this is the closest to what you were looking for: https://pmc.ncbi.nlm.nih.gov/articles/PMC3931018/#sec3

    Yeah, that covers nicely what I was wondering about. Especially the reason 1 (embryonic proteins not present during immune system education) and reason 2 (epigenetic changes). I can appreciate that these mechanisms might possibly cause issues, but I would be curious to learn the actual magnitude of their impact.

    Yamanaka named iPSCs with a lower case “i” due to the popularity of the iPod and other products.

    Oooh, that’s why! I do think iPSC looks nicer than IPSC. Not a big apple fan, though



  • How did I miss that?!

    My timeline is incorrect then. Since the post from sassymetischick.bsky predates the wiki edit, it is more likely that the wiki edit was made in response to this meme, and not the other way around. This pretty invalidates what I said above…

    I still can’t find any evidence of this being an actual trend, but I no longer have a good guess about the origin.




  • Salamander@mander.xyzMtoScience Memes@mander.xyzChat, is this true?
    link
    fedilink
    English
    arrow-up
    43
    ·
    edit-2
    2 months ago

    EDIT: As indepndnt mentioned in a comment below, the OP was posted on February 14, which pre-dates the wikipedia edits. So, my conclusions below about the timeline are not valid.

    Hah, sure, let’s investigate 🕵️‍♂️

    The term ‘Chalchiuhtlicueyecatl’ was added as a potential Aztec name to the English wikipedia page on February 15, 2025, by user ‘Mxn’.

    The description of the edit is the following:

    Frum says the Aztecs had no specific name for the gulf, which is plausible in a practical sense, but Fernández gives a specific religious name and is more of a reliable source on this topic

    If we investigate a bit further, we can see that the term Chalchiuhtlicueyecatl is described to be a name for the ‘Gulf of Mexico’ in the spanish Wikipedia: https://es.wikipedia.org/wiki/Chalchiuhtlicueyecatl

    This page was updated to include the description of Chalchiuhtlicueyecatl as the ‘Gulf of Mexico’ in September 16, 2018. I don’t have access to the citation so I don’t know if the citation specifies if this term is still known/used.

    If you check the history you will find that the same ‘Mxn’ fixed a typo in this page on February 15, 2025.

    So, from this sequence of events it is highly likely that the term ‘Chalchiuhtlicueyecatl’ was included into the Gulf of Mexico wiki page as a result of the user Mxn performing an active search for Aztec names for the Gulf of Mexico, and finding this connection between the term an the gulf by searching on Wikipedia. This information did not come from recent news about the term being used by natives.

    I can find no evidence of native people referring to the gulf of Mexico as ‘Chalchiuhtlicueyecatl’ more frequently or at all. I can find no mention of this becoming viral in Mexico.

    I find it highly unlikely that:

    • User Mxn added an obscure Aztec term to the Wiki page two weeks ago

    AND

    • This same obscure Aztec term coincidentally began being used by Mexican natives, and this trend became popular enough to be noticed by foreign media but not by Mexican media

    More likely…

    • Mxn actively looked for a term and updated the English wiki
    • Someone read the English wiki, thought this would be a nice story, made the meme

    And this concludes my little investigation 🧐


  • Always exciting to learn about new perspectives on consciousness!

    I have searched for the “Cellular Basis of Consciousness (CBC)” theory and I do not personally find it very compelling. I appreciate that the hard problem of consciousness is very difficult to address using the scientific method, but I suspect that consciousness arises from a form of processing that requires computations of the kind performed by animal brains. I don’t think that the kind of biophysics that allows cells to sense and respond to the environment are enough to create a conscious experience.

    About the: “third state”. Cells are alive, independently of the multi-cellular organism that they come from. I don’t agree that changing the way that the cells are organized constitutes some “third state”.

    Despite my disagreements, it is still nice to read and think about. Thanks for sharing.


  • Interesting! I wonder if it is already technically feasible to culture tooth-like pieces from the patient’s stem cells. Instead of extracting and carving a tooth, it would be cool to grow the tissue in some kind of structured 3D matrix. Patient gets to keep their canine then.

    That said… Do you know if tissue grown from a patient’s own stem cells is generally not rejected by the immune system? I am not sure if cells need to differentiate within the body to get labeled by some molecular markers that make them immunocompatible, or if having the same genetic makeup is good enough.


  • I think it would be an interesting hypothesis to test.

    I looked a bit more and extended my search into brines, and was able to find another set of data in the following paper:

    Roupas, P., Keogh, J., Noakes, M., Margetts, C., & Taylor, P. (2010). Mushrooms and agaritine: A mini-review. Journal of Functional Foods, 2(2), 91-98.

    This one is not freely available, but it is found in SciHub and I can also share the PDF if needed.

    This relevant section discusses that mushrooms canned in liquid and in brine were measured to have less agaritine, which makes sense. I think that lactofermentation helps degrade even more due to the acid, additional metabolic activity, and possibly a bit more oxygen.

    I agree that it would be nice to research. I am surprised that it hasn’t been (or at least it is not easy to find). I did find research on other methods such as heating and drying, but I could not find lacto fermentation…

    Agaritine content of mushrooms

    The agaritine content in fresh A. bisporus mushrooms in Swit- zerland has been reported to be in the range of 94–629 mg/kg fresh weight. Canned mushrooms contained 1–55 mg/kg drained weight with 3–103 mg/L in the liquid. The highest agaritine values were reported in dried commercial mush- rooms amounting to 2110–6905 mg/kg (Fischer et al., 1984). In Sweden, Andersson et al. (1999) measured agaritine in fresh mushrooms and 35 canned mushroom products (A. bisporus). Two fresh samples contained 212 and 229 mg/kg, respectively. Agaritine levels in brine were generally slightly lower than the levels detected in canned mushrooms. Canned whole mushrooms contained 14.9 ± 6.7 mg agaritine per kg product whereas cut mushrooms contained 18.1 ± 7.8 mg/kg. The wet canning process was shown to reduce the level of agaritine in A. bisporus by 10-fold resulting in lower levels in canned products. On a portion basis, somewhat higher amounts of agaritine may be found in some other food prod- ucts (mushroom soup and pasta sauce) containing A. bisporus (Andersson et al., 1999).


  • Yes, this is what I mean.

    As for (3), this is how I am reasoning about this. The mushroom cells are surrounded by a soft cell membrane made out of lipids, and a hard cell wall made out of a network of sugar filaments (primarily chitin). The cell membrane serves as a chemical barrier that separates the chemistry outside of the cell from the chemistry inside of the cell, and it has many mechanisms to allow specific chemicals to flow from one side to the other. This cell membrane is very dynamic and it needs continuous maintenance to remain functioning as intended. When a cell dies, the cell membrane is no longer kept under maintenance, and it basically dissolves.

    After the cell membrane disintegrates, the cell wall remains. This cell wall is much tougher and does not require constant maintenance. The wall also has its own filtering capacity as well the ability to absorb and retain chemicals, but it is a lot more porous and this porosity allows water, nutrients, and other water-soluble chemicals to move more freely.

    So, my reasoning is: The mushroom dies. The cell wall disintegrates. The more permeable cell wall remains. Agaritine is soluble in water, and water and small water-soluble molecules can usually move freely through the cell wall. So, within a short period of time the water outside of the mushrooms will mix with the water inside of the mushrooms, and the agaritine will distribute throughout the whole volume. At this point, even if the mushroom’s environment had provided some form of protection, the now-mixed agaritine will experience an environment similar to the environments discussed in the papers I from the previous comments.

    It is not as simple as I describe here, because the specific properties of the cell wall can be complex, and they can change due to chemical modifications. For example, some molecules can be absorbed into the sugar matrix such that they are protected from degradation - but I could not find any data to suggest that this likely a significant factor for agaritine. There are some recent articles that review the fungal cell wall, I will paste the citations below, in case you want to look at some of this in more detail.

    Gow, N. A., & Lenardon, M. D. (2023). Architecture of the dynamic fungal cell wall. Nature Reviews Microbiology, 21(4), 248-259.

    Latgé, J. P., & Wang, T. (2022). Modern biophysics redefines our understanding of fungal cell wall structure, complexity, and dynamics. Mbio, 13(3), e01145-22.


  • My question has to do about the agaritine content in mushrooms that are subjected to fermentation. That agaritine might behave differently when contained in a mushroom. What answer to my question does the articles give you?

    It is true. I am not sure, the articles do not address this specific question. It would depend on the process and the amount of time that you let it ferment. Over a period of weeks, it is likely that the mushrooms will have died, the cell membranes will have broken down, and the chemistry of degradation described in those papers will have taken place.

    Fresh mushrooms are still alive at the beginning of the process. Until they die, the mushroom’s cells may continue to produce agaritine, and the chemistry inside of the cells is not necessarily going to be the same as in tap water. The amount of time that it will take for the cells to die depends on the process. If you are submerging the mushrooms into a brine, I don’t think that they will survive for long because of the osmotic pressure.


  • No problem! I searched “Agaritine degradation” in Google Scholar and selected to those two articles from the results page as they seemed relevant. I also searched for more specific fermentation based papers but did not find any - this is what I mean when I say quick search.

    I did not use an LLM chat bot to formulate the answer, but I did copy and paste it to ChatGPT and asked whether it agreed. I often do this in case it catches some obvious mistake. But it did not suggest any corrections, and it did not affect my answer. So an LLM chatbot did assist me in validation.

    If you want I can explain some of the reasoning in more detail. Figures 1 and 3 of the first paper have data on what happens when agaritine is dissolved in water in the presence of air (‘open vial’), no air (‘closed vial’), and at a low pH with a closed vial. I think that these two figures are the most relevant to this particular question, as they give you an estimate to how fast agaritine will break down due to conditions that are easy to control and measure. Other types of microbiological activity can have an effect, but in this case it is not essential to invoke these more complicated processes.


  • Short summary from a quick search in the literature: Agaritine in water degrades quickly if oxygen is present, so if you can have an extended amount of time during which the mixture of water and ground mushroom is exposed to fresh air, that will help. As the mixture becomes acidic, degradation speeds up again even if the the atmosphere becomes oxygen poor. If the fermentation is meant to take more than 3 weeks, the acidic environment will probably be enough. Enzymes from the microbes are likely to have a combined effect that ultimately speeds up degradation as well, but that is a more complicated process and so it is not so easy to estimate the rates.


    Low pH, exposure to water, oxygen, and time will help. It seems like it degrades quite quickly in water if oxygen is present, but in lacto fermentation you do want to create an anaerobic environment so you might have a quick degradation followed by the formation of a protective atmosphere.

    The lowering of the pH will then help speed up the degradation again, but not as much as oxygen does.

    Have a look at the following paper to see curves of how agaritine degrades in water in the presence of fresh air, in a closed vial, at different pH levels:

    Hajšlová, J., Hajkova, L., Schulzova, V., Frandsen, H., Gry, J., & Andersson, H. C. (2002). Stability of agaritine-a natural toxicant of Agaricus mushrooms. Food Additives & Contaminants, 19(11), 1028-1033.

    Since you have a microbiologically active community, you also have access to the enzymatic pathways. I have not found a specific paper about agaritine during fermentation. I can find other articles describing enzymatic transformations and degradation. Some of these transformations can change the molecule into more toxic forms, and other enzymes move it towards a degraded product. What I expect that you will see is that the net effect of having a complex enzymatic mixture will be faster degradation, even if the pathways may cross the more active toxic intermediates (which would also probably form in your intestine), these will only form for a short time and degrade.

    You can refer to the paper below for specific examples of the enzymatic transformations that I am referring to. In this paper, the enzymes come from mushrooms that are ground into a liquid, and so they are mushroom enzymes. In the context of fermentation the source of the enzymes would be excreted by the fermenters into the ferment. These enzymes would likely not be specifically evolved for agaritine but instead represent general classes of enzymes that affect functional groups that are present in agaritine. It is difficult to make specific predictions.

    Walton, K., Coombs, M. M., Walker, R., & Ioannides, C. (2001). The metabolism and bioactivation of agaritine and of other mushroom hydrazines by whole mushroom homogenate and by mushroom tyrosinase. Toxicology, 161(3), 165-177.






  • Even though:

    These data are associative and do not establish a causal role for such particles affecting health

    I still don’t feel so nonchalant about the idea of microplastics lodging on my brain. While the effect on human brains is very difficult to directly measure, we do have a lot of data on mice that suggest that having plastic in the brain is bad for the brain.

    When quickly looking into EU food regulations it seems like microplastic content is not regulated in food, and the logic appears to be along the lines that not enough data is available to assess the actual risk. This makes some sense in that measurement, control, and enforcing limits is likely to be difficult, expensive, and might create some economic challenges, and so regulators might not want to go this route unless proven absolutely necessary.

    At the same time, data does exist showing that the plastic levels are increasing in our brains, and we have very good reasons to believe that this is not a good thing. It is not that we are completely in the dark - I am sure some smart people would be able to come up with reasonable limits and methods of control by now.

    My not-very-informed suspicion is that there is pressure from wealthy and powerful lobbyists that would significantly suffer from microplastics regulations, because ‘plastic in the brain’ has seemed like an obvious thing to address for some years now.

    I have never been educated about how to avoid ingesting / breathing microplastics. Do any of you know some habits or diets that reduce or increase exposure to microplastics?