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Peer-reviewed articleOpen access

<i>In vitro</i> and <i>in vivo</i> metabolism of psilocybin's active metabolite psilocin.

Thomann JiD, Kolaczynska KE, Stoeckmann OV, Rudin DiD, Vizeli P, Hoener MCiD, Pryce CRiD, Vollenweider FX, Liechti MEiD, Duthaler UiD

Frontiers in pharmacologyApr 29, 2024License: open accessSwitzerland48 citationsDOI: 10.3389/fphar.2024.1391689

Abstract

<i>In vivo</i>, psilocybin is rapidly dephosphorylated to psilocin which induces psychedelic effects by interacting with the 5-HT<sub>2A</sub> receptor. Psilocin primarily undergoes glucuronidation or conversion to 4-hydroxyindole-3-acetic acid (4-HIAA). Herein, we investigated psilocybin's metabolic pathways <i>in vitro</i> and <i>in vivo</i>, conducting a thorough analysis of the enzymes involved. Metabolism studies were performed using human liver microsomes (HLM), cytochrome P450 (CYP) enzymes, monoamine oxidase (MAO), and UDP-glucuronosyltransferase (UGT). <i>In vivo</i>, metabolism was examined using male C57BL/6J mice and human plasma samples. Approximately 29% of psilocin was metabolized by HLM, while recombinant CYP2D6 and CYP3A4 enzymes metabolized nearly 100% and 40% of psilocin, respectively. Notably, 4-HIAA and 4-hydroxytryptophol (4-HTP) were detected with HLM but not with recombinant CYPs. MAO-A transformed psilocin into minimal amounts of 4-HIAA and 4-HTP. 4-HTP was only present <i>in vitro</i>. Neither 4-HIAA nor 4-HTP showed relevant interactions at assessed 5-HT receptors. In contrast to <i>in vivo</i> data, UGT1A10 did not extensively metabolize psilocin <i>in vitro</i>. Furthermore, two putative metabolites were observed. <i>N</i>-methyl-4-hydroxytryptamine (norpsilocin) was identified <i>in vitro</i> (CYP2D6) and in mice, while an oxidized metabolite was detected <i>in vitro</i> (CYP2D6) and in humans. However, the CYP2D6 genotype did not influence psilocin plasma concentrations in the investigated study population. In conclusion, MAO-A, CYP2D6, and CYP3A4 are involved in psilocin's metabolism. The discovery of putative norpsilocin in mice and oxidized psilocin in humans further unravels psilocin's metabolism. Despite limitations in replicating phase II metabolism <i>in vitro</i>, these findings hold significance for studying drug-drug interactions and advancing research on psilocybin as a therapeutic agent.

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Psilocybin

Keywords

MetabolismPharmacokinetics5-HT receptorliver microsomesRecombinant EnzymesCytochrome P450 (Cyp)Psychedelics

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