Pharmacokinetics of Psilocybin, a Tryptamine Alkaloid in Magic Mushroom (Psilocybe cubensis): A Systematic Review

被引:0
|
作者
Thaoboonruang, Nilubon [1 ,2 ]
Lohitnavy, Manupat [1 ,2 ,3 ]
Lohitnavy, Ornrat [1 ,2 ,3 ]
机构
[1] Naresuan Univ, Fac Pharmaceut Sci, Ctr Excellence Environm Hlth & Toxicol, Phitsanulok 65000, Thailand
[2] Naresuan Univ, Fac Pharmaceut Sci, Pharmacokinet Res Unit, Phitsanulok, Thailand
[3] Naresuan Univ, Fac Pharmaceut Sci, Dept Pharm Practice, Phitsanulok, Thailand
关键词
Magic mushroom; pharmacokinetics; Psilocin; Psilocybin; Psilocybe cubensis; systematic review; PERFORMANCE LIQUID-CHROMATOGRAPHY; LIFE-THREATENING CANCER; RAT PLASMA; DEPRESSION; DEPHOSPHORYLATION; PSYCHEDELICS; ANXIETY;
D O I
10.1080/02791072.2024.2399128
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Psilocybin, a major indole alkaloid found in magic mushrooms (Psilocybe cubensis), has recently drawn attention as a breakthrough therapy to treat major depressive disorder. This review aimed to summarize and identify knowledge gaps concerning their pharmacokinetic characteristics of psilocybin and its active metabolite, psilocin. Original studies related to pharmacokinetics of psilocybin conducted in vitro, animals, and humans were systematically collected from PubMed, Scopus, and ScienceDirect, from their inceptions to November 2023. Twenty articles were included in this work and assessed for study quality. A comprehensive review of the pharmacokinetics of psilocybin and psilocin in both animals and humans was performed. Psilocybin is considered a prodrug that is dephosphorylated to psilocin by alkaline phosphatase. Following ingestion, the peak psilocin plasma and brain levels were rapidly achieved in a dose-dependent manner. Psilocin is metabolized primarily through both Phase I and Phase II processes with the half-life of 2-3 hours. This review also identified lack of some pharmacokinetic related information and limitations of available research that may help direct future investigations to better understand the pharmacokinetics and improve study design including dose selection and dosage optimization.
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页数:13
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