ChristianBonanno
Active Member
i’m sorry, but you can’t say “research shows” and not show me any of the research.
Unfortunately one of the flaws found in medical research is that each piece of research has to be based on a theory, a philosophy if you will. The researcher sets out to prove, or disprove, that theory. We don't usually get to read researchers self-disproven theories but it is common to read researchers trying to disprove each others theories. Even those of us who post on these forums possess unique theories/philosophies, based on what we have read to date, which determine the suggestions we are likely to write. In my own case that research has been pointing me towards elevated levels of certain types of bacteria which are associated with the health issues which I have. The research into those types of bacteria, and their metabolites and toxins, can get pretty confusing since there are often many factors which have to be considered. I do admit that I haven't previously looked at the research which you have posted, and do find the information on purines very interesting/potentially useful even though my own health issues don't involve them, but find the information on ATP, GTP, IMP, and XMP, irrelevant to my own philosophy for attempting to repair health via diet. I realise that they are intimately relevant to medical research and the development of drugs but they are unlikely to impact my choices of foods and supplements. One of the funny things which you find in medical research is that there usually isn't just one way to achieve an outcome, even if some are more effective than others. For myself it was a familial predisposition (relating to inherited microbiome) to gluten allergy and multiple sclerosis along with decades of working with heavy metals and industrial toxins in the glass industry which were the the original primary drivers for a dysregulated microbiome. It turned out that one substance, which we were told was safe to be exposed to, was burning holes in my gastrointestinal tract. Try repairing the microbiome when that is going on, lol.Yes, I agree with that study. But what I’m saying is that you have to go deeper than that to really understand what’s going on and how to correct it.
The gut Microbiome is affected by ATP, GTP IMP, and XMP
If you have too much of those are too little of those, your microbiome will not be able to control the environment in the gut and this will correlate with other symptoms like either depression, fatigue, mania, or anxiety, depending on whether they are higher or low.
It’s not that one causes the other, they both arise from the same fundamental issue of low or high basic purines.
Exploration of the link between gut microbiota and purinergic signalling - PMC
Growing evidence reveals that microorganisms in the gut are linked to metabolic health and disease risk in human beings to a considerable extent. The focus of research at this stage must tend to focus on cause-and-effect studies. In addition to ...www.ncbi.nlm.nih.gov
It is way more complicated to try to decide what specific balance of the thousands of microbes we need in our guts then it is to decide why we have balances in these basic purines.
More
ATP as a Pathophysiologic Mediator of Bacteria-Host Crosstalk in the Gastrointestinal Tract - PMC
Extracellular nucleotides, such as adenosine triphosphate (ATP), are released from host cells including nerve termini, immune cells, injured or dead cells, and the commensal bacteria that reside in the gut lumen. Extracellular ATP interacts with the ...www.ncbi.nlm.nih.gov
Unfortunately one of the flaws found in medical research is that each piece of research has to be based on a theory, a philosophy if you will. The researcher sets out to prove, or disprove, that theory. We don't usually get to read researchers self-disproven theories but it is common to read researchers trying to disprove each others theories. Even those of us who post on these forums possess unique theories/philosophies, based on what we have read to date, which determine the suggestions we are likely to write. In my own case that research has been pointing me towards elevated levels of certain types of bacteria which are associated with the health issues which I have. The research into those types of bacteria, and their metabolites and toxins, can get pretty confusing since there are often many factors which have to be considered. I do admit that I haven't previously looked at the research which you have posted, and do find the information on purines very interesting/potentially useful even though my own health issues don't involve them, but find the information on ATP, GTP, IMP, and XMP, irrelevant to my own philosophy for attempting to repair health via diet. I realise that they are intimately relevant to medical research and the development of drugs but they are unlikely to impact my choices of foods and supplements. One of the funny things which you find in medical research is that there usually isn't just one way to achieve an outcome, even if some are more effective than others. For myself it was a familial predisposition (relating to inherited microbiome) to gluten allergy and multiple sclerosis along with decades of working with heavy metals and industrial toxins in the glass industry which were the the original primary drivers for a dysregulated microbiome. It turned out that one substance, which we were told was safe to be exposed to, was burning holes in my gastrointestinal tract. Try repairing the microbiome when that is going on, lol.
The combined effect of all these pathways is a vicious cycle in which a defective axonal transport system leads to an increase in ATP consumption through loss of membrane organization and a reduction in available ATP through inhibition of mitochondrial transport, resulting in even further inhibition of transport. The persistent activity of this positive feedback loop contributes to neurodegeneration in MS.
Actually I never developed the familial multiple sclerosis. From what I have read that's likely to be the combination of greater sun exposure/vitamin D production and my love for Asian food containing antimicrobials. Over the years I have repaired various conditions, such as industrial solvent induced chronic fatigue, lactose intolerance, sciatica, and so on. My current condition (myositis, impaired respiratory function, and a range of other health issues/diseases) has been solely the result of medical incompetence and systemic denial, which I am currently registering a comprehensive complaint to the government in regards to.
I have considered whether it could be possible to determine our inherited microbiome from the composition of the microbiome in our colons. The high risks (possible death or disease) of faecal microbiota transplants make them very unappealing but it is still interesting that, by implanting the faecal microbiota from healthy individuals into people with inherited diseases they have been able to reverse or cure such conditions. https://multiplesclerosisnewstoday....l-ms-trial-shows-safety-potential-enrich-gut/ That makes me think that it is this region of our gastrointestinal tract where the inherited microbiome is much more resilient to change by diet after early childhood, with the transplants resulting in significant change.
I used to think that it was essential to know my genetic profile, and am still hoping to obtain a comprehensive test at some point, however recent research has been demonstrating that gene variants aren't necessarily inherited. It seems that our microbiome is able to cause gene variants in at least some cases, with the possibility that further research may well prove that the microbiome regulates them all. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680557/
First, a genetic variant may directly cause the disease phenotype, resulting in an altered microbiome as a consequence of the disease phenotype. Second, a genetic variant may alter gene expression in the host, which in turn alters the microbiome, producing the disease phenotype.
https://www.nature.com/articles/nrg.2017.63 There is now sufficient research, connecting levels of specific bacteria with specific host gene variants to either pose the argument that the variants influence the microbiome or the reverse. While some, more arrogant, researchers pose the first argument https://pubmed.ncbi.nlm.nih.gov/37827115/ others are much more cautious https://www.pnas.org/doi/full/10.1073/pnas.2200551119 An enormous number of so-called facts which were taught in school have been disproven over the decades proving that making pompous declarations doesn't prove arguments. The association between specific microbial expressions associated with specific gene variants has not yet been explained as figure one in this article details. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295090/ As the following article states; Gut microbiota has a widespread and modifiable effect on host gene regulation.
Perhaps you just need to study more.