Psilocin acutely disrupts sleep and affects local but not global sleep homeostasis in laboratory mice
This mouse study (n=8) investigated the effects of psilocin (2 mg/kg; 56mg/28g mouse weight) on the normal sleep-wake cycle and in combination with sleep deprivation. Results indicated that psilocin acutely disrupts sleep, suppressing the maintenance of both NREM and REM sleep, resulting in a pattern of fragmented sleep attempts and frequent brief awakenings which lasted up to 3 hours. No enduring effects of psilocin were observed on sleep-wake quantities, sleep duration, or the recovery from sleep deprivation.
Abstract
Introduction
Serotonergic psychedelic drugs, such as psilocin (4-hydroxy-N,N-dimethyltryptamine), profoundly alter the quality of consciousness through mechanisms which are incompletely understood. Growing evidence suggests that a single psychedelic experience can positively impact long-term psychological well-being, with relevance for the treatment of psychiatric disorders, including depression. A prominent factor associated with psychiatric disorders is disturbed sleep, and the sleep-wake cycle is implicated in the regulation of neuronal firing and activity homeostasis. It remains unknown to what extent psychedelic agents directly affect sleep, in terms of both acute arousal and homeostatic sleep regulation.
Methods
Here, chronic in vivo electrophysiological recordings were obtained in mice to track sleep-wake architecture and cortical activity after psilocin injection.
Results
Administration of psilocin led to delayed REM sleep onset and reduced NREM sleep maintenance for up to approximately 3 hours after dosing, and the acute EEG response was associated primarily with an enhanced oscillation around 4 Hz. No long-term changes in sleep-wake quantity were found. When combined with sleep deprivation, psilocin did not alter the dynamics of homeostatic sleep rebound during the subsequent recovery period, as reflected in both sleep amount and EEG slow wave activity. However, psilocin decreased the recovery rate of sleep slow wave activity following sleep deprivation in the local field potentials of electrodes targeting medial prefrontal and surrounding cortex.
Discussion
It is concluded that psilocin affects both global vigilance state control and local sleep homeostasis, an effect which may be relevant for its antidepressant efficacy.
Research Summary of 'Psilocin acutely disrupts sleep and affects local but not global sleep homeostasis in laboratory mice'
Introduction
Psilocybin and its active metabolite psilocin are classical serotonergic psychedelics that profoundly alter perception and cognition, and emerging evidence indicates that a single psychedelic exposure can produce lasting improvements in mood and psychological well-being. Much of the hypothesised therapeutic action of these drugs is thought to involve 5-HT2A receptor-mediated changes in cortical dynamics and neuroplasticity, but how these effects interact with the sleep-wake cycle and sleep-dependent plasticity mechanisms is not well understood. Disturbances of sleep and dysregulation of sleep homeostasis are prominent features of many psychiatric disorders, including depression, and sleep slow wave activity (SWA, 0.5–4 Hz) is widely used as a physiological marker of the brain’s homeostatic sleep drive (Process S). This study set out to characterise acute and subsequent effects of psilocin on sleep-wake behaviour and cortical electrophysiology in mice. Specifically, Thomas and colleagues administered psilocin and vehicle to the same animals under two conditions (undisturbed post-injection sleep and enforced wakefulness via sleep deprivation) and recorded EEG, local field potentials (LFPs) and multi-unit activity to assess vigilance-state architecture, spectral signatures and both global and local indices of sleep homeostasis.
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Study Details
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Thomas, C. W., Blanco-Duque, C., Bréant, B., Goodwin, G. M., Sharp, T., Bannerman, D. M., & Vyazovskiy, V. V. (2021). Psilocin acutely disrupts sleep and affects local but not global sleep homeostasis in laboratory mice. https://doi.org/10.1101/2021.02.16.431276
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