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Introduction Psilocybin is one of the most extensively studied psychedelic drugs with a broad therapeutic potential. Despite the fact that its psychoactivity is mainly attributed to the agonism at 5-HT 2A receptors, it has high binding affinity also to 5-HT 2C and 5-HT 1A receptors and indirectly modulates the dopaminergic system. Psilocybin and its active metabolite psilocin, as well as other serotonergic psychedelics, induce broadband desynchronization and disconnection in EEG in humans as well as in animals. The contribution of serotonergic and dopaminergic mechanisms underlying these changes is not clear. The present study thus aims to elucidate the pharmacological mechanisms underlying psilocin-induced broadband desynchronization and disconnection in an animal model. Methods Selective antagonists of serotonin receptors (5-HT 1A WAY100635, 5-HT 2A MDL100907, 5-HT 2C SB242084) and antipsychotics haloperidol, a D 2 antagonist, and clozapine, a mixed D 2 and 5-HT receptor antagonist, were used in order to clarify the underlying pharmacology. Results Psilocin-induced broadband decrease in the mean absolute EEG power was normalized by all antagonists and antipsychotics used within the frequency range 1–25 Hz; however, decreases in 25–40 Hz were influenced only by clozapine. Psilocin-induced decrease in global functional connectivity and, specifically, fronto-temporal disconnection were reversed by the 5-HT 2A antagonist while other drugs had no effect. Discussion These findings suggest the involvement of all three serotonergic receptors studied as well as the role of dopaminergic mechanisms in power spectra/current density with only the 5-HT 2A receptor being effective in both studied metrics. This opens an important discussion on the role of other than 5-HT 2A -dependent mechanisms underlying the neurobiology of psychedelics.
Tylš et al. (Thu,) studied this question.