Concurrent stress modulates the acute and post-acute effects of psilocybin in a sex-dependent manner
Chloé Galipeau, Zsolt Lenkei, Miguel Farinha‐ferreira, Catarina Miranda‐lourenço, Ana M. Sebastião
Neuropharmacology December 24, 2024 DOI: 10.1016/j.neuropharm.2024.110280 via OpenAlex
Summary
AI-generated from the abstractPsilocybin increased head-twitch responses in both male and female mice, with a greater effect in females. Stress during the drug's acute effects blocked psilocybin's anxiety-reducing actions in males but only partially in females; no antidepressant-like effects were observed. Both stress and psilocybin independently raised corticosterone levels without additive or interactive effects. The findings highlight how sex and negative experiences during the drug's action influence its acute and post-acute mood effects, underscoring the importance of non-pharmacological factors for therapeutic and recreational use.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Adult male and female C57BL/6J mice |
| Intervention | Psilocybin |
| Dose | 5 mg/kg |
| Duration | 1-hour restraint during acute drug effects; behavioral tests starting 24 hours after administration |
| Topics | Psilocybin |
| Keywords | Hallucinogen Acute pain Medicine Pharmacology |
| Citations | 17 |
| Key finding | Psilocybin induced anxiolytic-like effects that were fully blocked by stress in males but only partially in females, with no antidepressant-like effects observed. |
Abstract
There is renewed interest in psychedelics, such as psilocybin, as therapies for multiple difficult-to-treat psychiatric disorders. Even though psychedelics can induce highly pleasant or aversive experiences, depending on multiple personal and environmental factors, there is little research into how such experiences impact post-acute mood-altering actions. Here we aimed at offsetting this gap. First, we tested whether acute psilocybin effects differed between sexes. Adult male and female C57BL/6J mice received saline or psilocybin (5 mg/kg; i.p.), and head-twitch response (HTR) frequency was quantified. Notably, while psilocybin increased HTR frequency in both sexes, the effect was greater in females. We then tested if stress exposure during acute drug effects impacted post-acute psilocybin actions. Following drug treatment, mice were returned to their homecage or restrained for 1 h. Anxiety- and depression-like behaviors were assessed starting 24 h following drug administration, using the marble burying, novelty-suppressed feeding, and splash tests. Psilocybin induced anxiolytic-, but not antidepressant-like, which were fully blocked by stress in males, but only partially so in females. Lastly, we assessed the acute stress-psilocybin interaction on plasma corticosterone levels in a separate cohort of mice, treated as above. Both stress and psilocybin independently increased corticosterone levels, without additive or interactive effects being observed for either sex. Our data reveals the role of sex and peri-acute negative experiences in the acute and post-acute actions of psilocybin. These findings underline the importance of non-pharmacological factors, such as the quality of the psychedelic experience, in the mood-altering effects of psychedelics, holding significant for both their therapeutic and recreational use.