Sabnock1990
Be Your Own Shaman
Somebody should seriously do a study using proper B12, Folate and B6 + Tryptophan (with or without MAO-A inhibition), even on rats, to test endogenous Tryptamine (and NMT/DMT) levels. It would be nice if that were legitimately scientifically studied, because i know for a fact it works, so i think it would make an interesting study.
Without going too in depth on the mechanisms and how these specific nutrients (as well as a few others) can influence and enhance endogenous Tryptamine/NMT/DMT synthesis, basically B6 (P5P) is needed by AADC/DOPA Decarboxylase which decarboxylates Tryptophan into Tryptamine, active B6 (P5P) needs to be taken with/at the same time as the Tryptophan because it forces Tryptophan down the decarboxylation route (otherwise Tryptophan without P5P will go along it's usual metabolic route only turning into Tryptamine like 7 hours or so later), and active Folate (Folinic Acid, or Methylfolate, not Folic Acid) as well as active B12 (Methylcobalamin, or alternatively Hydroxocobalamin, not Cyanocobalamin) are needed by Methionine Synthase to recycle Homocysteine back into Methionine so that the Methionine can go to Methionine Adenosyltransferase to turn Methionine into SAM which is needed for INMT. Tryptophan obviously provides the Tryptamine for methylation by INMT to NMT/DMT. MAO-A inhibition is imo ideal and probably necessary for proper activity of Tryptamine, NMT and DMT. Folic Acid can be a detriment for a few reasons, and Cyanocobalamin as well.
So when scientists are studying endogenous DMT levels, whether in rats or Humans, they should do some studies on this approach as well, making sure to address any underlying Folate or B12 or B6 deficiencies (which B12 and Folate are interlinked with each other and the B12 portion can be especially hard to detect compared to Folate, especially using blood tests which don't reliably detect B12 or Folate deficiency particularly in the brain where it matters most), and should also remove Folic Acid and Cyanocobalamin from the equation entirely, preferably, and should supply enough Folate, B12 and B6, as well as Tryptophan, for accurate brain DMT measurements, otherwise, rats deficient in these things or underactive in methylation may not be able to synthesize NMT/DMT from Tryptamine effectively.
I have taken these things a good handful of times while MAO-A is inhibited by the Harmalas, and most definitely, endogenous Tryptamine, NMT, and DMT are all noticed, and it works. However, it's anybody's guess as to how much the body/brain could theoretically synthesize if given sufficient enough substrate/precursors/co-factors for endogenous Tryptamine/NMT/DMT synthesis, but ime it "can" be on par with at least a mildly moderate dose of at least oral NMT equivalent, that much is for sure so far. It's also worth keeping in mind that NMT is the direct precursor to DMT, so even if it's mainly NMT (methylated Tryptamine) that is synthesized, at least some portion of that can go back through INMT again to become DMT, question is, how much DMT could INMT synthesize before DMT in turn inhibits INMT from further activity?
Basically, you need SAM for INMT to work and the BHMT enzyme isn't active in the brain like Methionine Synthase is so Homocysteine can't be recycled back to Methionine and thus to SAM if you don't have enough B12 or Folate, you need MAO-A inhibition for Tryptamine, NMT and DMT to become more active in the system, and B6 (P5P) needs to be taken at the same time as the Tryptophan to force it's decarboxylation route. And you can't just consume Methionine even though it directly feeds SAM synthesis, because once SAM is synthesized it goes on to methylate things and can become quickly broken down to SAH and then to Homocysteine which then needs the B12 and Folate to recycle it back to Methionine for further SAM synthesis and by not making sure of Folate and B12 and thus accounting for full SAM levels, you can't properly determine how much INMT activity or NMT/DMT there is.
This is a testable method, you can personally feel the Tryptamine itself, then you can feel the Tryptamine being methylated by INMT to NMT, and then DMT effects start becoming a bit more apparent. I've literally had the same effects/reactions to this as i have to all my oral and smoked DMT effects, so it's definitely happening, and everything about this can be shown scientifically and tested/reproduced. Someone should seriously get on that lol. The sooner we can crack Endo-DMT, the better
Without going too in depth on the mechanisms and how these specific nutrients (as well as a few others) can influence and enhance endogenous Tryptamine/NMT/DMT synthesis, basically B6 (P5P) is needed by AADC/DOPA Decarboxylase which decarboxylates Tryptophan into Tryptamine, active B6 (P5P) needs to be taken with/at the same time as the Tryptophan because it forces Tryptophan down the decarboxylation route (otherwise Tryptophan without P5P will go along it's usual metabolic route only turning into Tryptamine like 7 hours or so later), and active Folate (Folinic Acid, or Methylfolate, not Folic Acid) as well as active B12 (Methylcobalamin, or alternatively Hydroxocobalamin, not Cyanocobalamin) are needed by Methionine Synthase to recycle Homocysteine back into Methionine so that the Methionine can go to Methionine Adenosyltransferase to turn Methionine into SAM which is needed for INMT. Tryptophan obviously provides the Tryptamine for methylation by INMT to NMT/DMT. MAO-A inhibition is imo ideal and probably necessary for proper activity of Tryptamine, NMT and DMT. Folic Acid can be a detriment for a few reasons, and Cyanocobalamin as well.
So when scientists are studying endogenous DMT levels, whether in rats or Humans, they should do some studies on this approach as well, making sure to address any underlying Folate or B12 or B6 deficiencies (which B12 and Folate are interlinked with each other and the B12 portion can be especially hard to detect compared to Folate, especially using blood tests which don't reliably detect B12 or Folate deficiency particularly in the brain where it matters most), and should also remove Folic Acid and Cyanocobalamin from the equation entirely, preferably, and should supply enough Folate, B12 and B6, as well as Tryptophan, for accurate brain DMT measurements, otherwise, rats deficient in these things or underactive in methylation may not be able to synthesize NMT/DMT from Tryptamine effectively.
I have taken these things a good handful of times while MAO-A is inhibited by the Harmalas, and most definitely, endogenous Tryptamine, NMT, and DMT are all noticed, and it works. However, it's anybody's guess as to how much the body/brain could theoretically synthesize if given sufficient enough substrate/precursors/co-factors for endogenous Tryptamine/NMT/DMT synthesis, but ime it "can" be on par with at least a mildly moderate dose of at least oral NMT equivalent, that much is for sure so far. It's also worth keeping in mind that NMT is the direct precursor to DMT, so even if it's mainly NMT (methylated Tryptamine) that is synthesized, at least some portion of that can go back through INMT again to become DMT, question is, how much DMT could INMT synthesize before DMT in turn inhibits INMT from further activity?
Basically, you need SAM for INMT to work and the BHMT enzyme isn't active in the brain like Methionine Synthase is so Homocysteine can't be recycled back to Methionine and thus to SAM if you don't have enough B12 or Folate, you need MAO-A inhibition for Tryptamine, NMT and DMT to become more active in the system, and B6 (P5P) needs to be taken at the same time as the Tryptophan to force it's decarboxylation route. And you can't just consume Methionine even though it directly feeds SAM synthesis, because once SAM is synthesized it goes on to methylate things and can become quickly broken down to SAH and then to Homocysteine which then needs the B12 and Folate to recycle it back to Methionine for further SAM synthesis and by not making sure of Folate and B12 and thus accounting for full SAM levels, you can't properly determine how much INMT activity or NMT/DMT there is.
This is a testable method, you can personally feel the Tryptamine itself, then you can feel the Tryptamine being methylated by INMT to NMT, and then DMT effects start becoming a bit more apparent. I've literally had the same effects/reactions to this as i have to all my oral and smoked DMT effects, so it's definitely happening, and everything about this can be shown scientifically and tested/reproduced. Someone should seriously get on that lol. The sooner we can crack Endo-DMT, the better
