Cytochrome P450 Inhibition by Psilocybin and Psilocin: A Combined Molecular Dynamics and Enzymatic Screening Study
Andreia Machado Brito-Da-Costa, Mariana Carvalho, Ricardo Jorge Dinis-Oliveira, Áurea Madureira-Carvalho, Sérgio Filipe Sousa, Diana Dias Da Silva
RevSALUS - Revista Científica da Rede Académica das Ciências da Saúde da Lusofonia May 1, 2026 DOI: 10.51126/revsalus.v8isupii.46839 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | In vitro and in silico study Peer reviewed |
|---|---|
| Interventions | Psilocybin Psilocin |
| Measures | Vivid®CYP450 screening kits, IC50, MMGBSA, per-residue decomposition energy, hydrogen bonds |
| Topics | Psilocybin |
| Key points | Psilocin inhibited CYP2A6, CYP2B6, CYP2D6, CYP2E1, and CYP3A4 in vitro, with IC50 values of 2.06, 6.17, 11.89, 6.37, and 2.36 mM, respectively. Molecular dynamics simulations indicated stronger binding affinity for psilocin than psilocybin, with specific hydrogen bonds and residues identified for each enzyme. The authors suggest a potential for psilocin to inhibit all five enzymes, especially CYP2A6 and CYP3A4. |
Abstract
Psilocybin is a hallucinogen produced by “magic mushrooms”, being rapidly metabolized in the organism into psilocin (Brito-da-Costa et al., 2022; Dinis-Oliveira, 2017). A scientific gap exists regarding the possible interactions between psilocybin/psilocin and CYP450 enzymes. Given their biological importance and since the binding of drugs to CYP450 enzymes can interfere with the metabolism of other substrates, leading to drug-drug interactions (Deodhar et al., 2020), this research topic is of utmost importance. This study aimed to evaluate in silico and in vitro the interaction of psilocybin and psilocin with the enzymes CYP2A6/2B6/2D6/2E1/3A4. The in vitro assessment of inhibition was performed using the Vivid®CYP450 screening kits. IC50 was calculated using GraphPad Prism 9.3.0. For in silico assessment, molecular dynamics were performed using the PMEMD.cuda module in AMBER16. Calculations were made on the last 100 ns of the trajectory (stable zone) to assess the interaction between enzyme and ligand, namely MMGBSA, per-residue decomposition energy, and hydrogen bonds. Psilocin showed the capacity to be an inhibitor of CYP2A6/2B6/2D6/2E1/3A4, based on the respective IC50 values (mM) of 2.06, 6.17, 11.89, 6.37, and 2.36. Considering the MMGBSA, higher values were obtained for psilocin, corroborating the stronger binding affinity of this compound. The interaction of psilocybin/psilocin with CYP2A6 is mediated by a hydrogen bond established with the protein residue Asn297. Other important residues include Phe107 and Ile366. For CYP2B6, the strong binding of psilocin is mediated by interactions with Ile114, Thr302 (hydrogen bond), and Leu363. For interaction with CYP2D6, the most important residue seems to be Ser304, with which it forms a hydrogen bond; for CYP2E1, key residues include Phe207, Thr303, and Phe478. A strong hydrogen bond is formed between psilocin and CYP3A4 residue Phe304, contributing to the high binding affinity. The results suggest a potential for psilocin to inhibit all enzymes, especially CYP2A6 and CYP3A4.
Comparable studies
Other preclinical and animal studies on psilocybin, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| Psilocybin induces rapid and persistent growth of dendritic spines in frontal cortex in vivo Mice | 2021 | Observational cohort | |
| Harnessing psilocybin: antidepressant-like behavioral and synaptic actions of psilocybin are independent of 5-HT2R activation in mice Mice | 2021 | Experimental study | |
| Psychedelics reopen the social reward learning critical period Mice | 2023 | Experimental study in mice | |
| Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species. C57BL/6J mice | 2020 | Experimental study with dose-response experiments | |
| Effects of psilocybin on hippocampal neurogenesis and extinction of trace fear conditioning Mice | 2013 | Experimental study |