BringsUsTogether
Rising Star
Rick Strassman's research as published in his book "DMT - The Spirit Molecule" led him to conclude that DMT could not always produce what he called "unitive mystical," "white light," or "near death" experiences. In fact, only a small percentage of his patients did.
Rick also mentioned later that these "white light/near death" experiences were more common on 5-Meo-DMT. However, 5-Meo-DMT is unlikely to be the "spirit molecule" because as far as we know, acetylserotonin O-methyltransferase O-methylates serotonin AFTER it is acetylated into acetylserotonin, and if we expect endogenous 5-Meo-DMT to be biosynthesized by INMT through N-methylation of 5-Meo-T, the 5-Meo-T should theoretically appear in only very low concentrations following deacetylation of melatonin.
The psychoactivity of bufotenine, however, is disputed. According to Wikipedia, recent studies have shown that if bufotenine is psychoactive, it's effects are similar to 5-Meo-DMT in nature. Many who have tried ingesting bufotenine find it to have little activity, however, I believe this is mainly caused by 5-hydoxy tryptamines being unable to cross the blood brain barrier because they are too polar.
http://bitnest.ca/external.php?id=%257DbxUgY%255CC%251A%2505%2506pg%257C%2506%2505RCW%250AM%2540w%257F%2560%2515Hk
according to this paper, bufotenine may have a hard time getting to the brain because of its low chloroform-water partition coefficient. However, 5-Aco-DMT, which metabolizes into bufotenine and has a higher partition coefficient, appears to be very active due to the high percentage of CAR failures (in fact, based on the results, it is not unlikely that 5-Aco-DMT is more active than 5-Meo-DMT!).
If we continue to follow the theory that INMT is responsible for methylation of tryptamine compounds, and that formation of psychoactive chemicals are at least partially responsible for near death/mystical experiences, it makes intuitive sense that bufotenine could be a potential "spirit molecule," since tryptamine and 5-Meo-T concentrations in the brain are low compared to those of serotonin. (INMT can methylate serotonin into bufotenine) & (tryptophan molecules are likely to be hydroxylated before being decarboxylated, as seen in the biosynthesis pathway for serotonin.)
Rick also mentioned later that these "white light/near death" experiences were more common on 5-Meo-DMT. However, 5-Meo-DMT is unlikely to be the "spirit molecule" because as far as we know, acetylserotonin O-methyltransferase O-methylates serotonin AFTER it is acetylated into acetylserotonin, and if we expect endogenous 5-Meo-DMT to be biosynthesized by INMT through N-methylation of 5-Meo-T, the 5-Meo-T should theoretically appear in only very low concentrations following deacetylation of melatonin.
The psychoactivity of bufotenine, however, is disputed. According to Wikipedia, recent studies have shown that if bufotenine is psychoactive, it's effects are similar to 5-Meo-DMT in nature. Many who have tried ingesting bufotenine find it to have little activity, however, I believe this is mainly caused by 5-hydoxy tryptamines being unable to cross the blood brain barrier because they are too polar.
http://bitnest.ca/external.php?id=%257DbxUgY%255CC%251A%2505%2506pg%257C%2506%2505RCW%250AM%2540w%257F%2560%2515Hk
according to this paper, bufotenine may have a hard time getting to the brain because of its low chloroform-water partition coefficient. However, 5-Aco-DMT, which metabolizes into bufotenine and has a higher partition coefficient, appears to be very active due to the high percentage of CAR failures (in fact, based on the results, it is not unlikely that 5-Aco-DMT is more active than 5-Meo-DMT!).
If we continue to follow the theory that INMT is responsible for methylation of tryptamine compounds, and that formation of psychoactive chemicals are at least partially responsible for near death/mystical experiences, it makes intuitive sense that bufotenine could be a potential "spirit molecule," since tryptamine and 5-Meo-T concentrations in the brain are low compared to those of serotonin. (INMT can methylate serotonin into bufotenine) & (tryptophan molecules are likely to be hydroxylated before being decarboxylated, as seen in the biosynthesis pathway for serotonin.)