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Sex differences and serotonergic mechanisms in the behavioural effects of psilocin

Filip Tylš, Tomáš Páleníček, L. Kadeřábek, Michaela Lipski, Anna Kubešová, Jiřı́ Horáček

Behavioural Pharmacology October 13, 2015 DOI: 10.1097/fbp.0000000000000198 via OpenAlex

Summary

AI-generated from the abstract

Psilocin, the active metabolite of psilocybin, produces dose-dependent inhibition of movement and suppression of normal behavior in rats, including behavioral serotonin syndrome and impaired prepulse inhibition. These effects are more pronounced in male rats than in females. The inhibition of locomotion is normalized by 5-HT 1A and 5-HT 2B/C receptor antagonists, but prepulse inhibition is not significantly affected by these antagonists. The findings highlight sex-specific reactions to psilocin and indicate that, in addition to 5-HT 2A-mediated effects, 5-HT 1A and 5-HT 2C/B receptors also play an important role, with implications for clinical trials.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Male and female rats
Interventions Psilocin WAY100635 MDL100907 SB215505 SB242084
Dose 0.25, 1 and 4 mg/kg psilocin; 1 mg/kg WAY100635; 0.5 mg/kg MDL100907; 1 mg/kg SB215505; 1 mg/kg SB242084
Topics Psilocybin Serotonin
Keywords Prepulse inhibition Receptor antagonist Pharmacology
Citations 86
Key finding Psilocin induces dose-dependent inhibition of locomotion and suppression of normal behavior, with effects more pronounced in male rats; locomotion inhibition is normalized by 5-HT 1A and 5-HT 2B/C antagonists, but prepulse inhibition is not significantly affected by these antagonists.

Abstract

Psilocybin has recently attracted a great deal of attention as a clinical research and therapeutic tool. The aim of this paper is to bridge two major knowledge gaps regarding its behavioural pharmacology – sex differences and the underlying receptor mechanisms. We used psilocin (0.25, 1 and 4 mg/kg), an active metabolite of psilocybin, in two behavioural paradigms – the open-field test and prepulse inhibition (PPI) of the acoustic startle reaction. Sex differences were evaluated with respect to the phase of the female cycle. The contribution of serotonin receptors in the behavioural action was tested in male rats with selective serotonin receptor antagonists: 5-HT 1A receptor antagonist (WAY100635 1 mg/kg), 5-HT 2A receptor antagonist (MDL100907 0.5 mg/kg), 5-HT 2B receptor antagonist (SB215505 1 mg/kg) and 5-HT 2C receptor antagonist (SB242084 1 mg/kg). Psilocin induced dose-dependent inhibition of locomotion and suppression of normal behaviour in rats (behavioural serotonin syndrome, impaired PPI). The effects were more pronounced in male rats than in females. The inhibition of locomotion was normalized by 5-HT 1A and 5-HT 2B/C antagonists; however, PPI was not affected significantly by these antagonists. Our findings highlight an important issue of sex-specific reactions to psilocin and that apart from 5-HT 2A -mediated effects 5-HT 1A and 5-HT 2C/B receptors also play an important role. These findings have implications for recent clinical trials.

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