DPT: Difference between revisions
>Mydriasis Added known fatality (see reference [6]) |
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{{pharmacology}} | {{pharmacology}} | ||
{{Further|Serotonergic psychedelic}} | {{Further|Serotonergic psychedelic}} | ||
Studies on rodents have found that the effectiveness with which a selective 5-HT<sub>2A</sub> receptor antagonist blocks the behavioral actions of this compound strongly suggest that the 5-HT<sub>2A</sub> receptor is an important site of action for DPT, but the modulatory actions of a 5-HT<sub>1A</sub> receptor antagonist also imply a 5-HT<sub>1A</sub>-mediated component to the actions of DPT.<ref>antegrossi WE, Reissig CJ, Katz EB, Yarosh HL, Rice KC, Winter JC (January 2008). "Hallucinogen-like effects of N,N-dipropyltryptamine (DPT): possible mediation by serotonin 5-HT1A and 5-HT2A receptors in rodents". ''Pharmacology, Biochemistry, and Behavior''. '''88''' (3): 358–65. doi:10.1016/j.pbb.2007.09.007. PMC 2322878. <nowiki>PMID 17905422</nowiki>.</ref> The role of these interactions and how they result in the [[psychedelic]] experience remains the subject of ongoing scientific investigation. | |||
The role of these interactions and how they result in the [[psychedelic]] experience remains the subject of ongoing scientific investigation. | |||
==Subjective effects== | ==Subjective effects== |