Sex-specific effects of psychedelic drug exposure on central amygdala reactivity and behavioral responding.
D P Effinger, S G Quadir, M C Ramage, M G Cone, M A Herman
Translational psychiatry April 8, 2023 DOI: 10.1038/s41398-023-02414-5 via PubMed
Summary
AI-generated from the abstractPsilocin, the active metabolite of psilocybin, produces sex-specific and lasting changes in central amygdala (CeA) activity and reactivity to an aversive stimulus in mice. Acutely, psilocin increased CeA activity in both sexes and increased stimulus-specific CeA reactivity in females but not males. Over time, psilocin decreased CeA reactivity in males from 2 to 28 days after administration, while no such decrease occurred in females. Behavioral responses to the aversive stimulus also showed sex-dependent changes in threat responding, without affecting exploratory behavior or locomotion. These findings indicate that a single dose of psilocin induces enduring, sex-specific alterations in CeA function and threat-related behavior.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Mice |
| Intervention | Psilocin |
| Duration | 28 days post administration |
| Keywords | Psychedelics Neuroscience Gender differences Mental health Brain research |
| Citations | 49 |
| Key finding | A single dose of psilocin produces sex-specific, time-dependent, and enduring changes in central amygdala reactivity and behavioral responding to an aversive stimulus. |
Abstract
Psilocybin and its active metabolite psilocin have been shown to elicit rapid and long-lasting symptom improvements in a variety of affective psychiatric illnesses. However, the region-specific alterations underlying these therapeutic effects remain relatively unknown. The central amygdala (CeA) is a primary output region within the extended amygdala that is dysregulated in affective psychiatric disorders. Here, we measured CeA activity using the activity marker c-Fos and CeA reactivity using fiber photometry paired with an aversive air-puff stimulus. We found that psilocin administration acutely increased CeA activity in both males and females and increased stimulus specific CeA reactivity in females, but not males. In contrast, psilocin produced time-dependent decreases in reactivity in males, but not in females, as early as 2 days and lasting to 28 days post administration. We also measured behavioral responses to the air-puff stimulus and found sex-dependent changes in threat responding but not exploratory behavior or general locomotion. Repeated presentations of the auditory component of the air-puff were also performed and sex-specific effects of psilocin on CeA reactivity to the auditory-alone stimulus were also observed. This study provides new evidence that a single dose of psilocin produces sex-specific, time-dependent, and enduring changes in CeA reactivity and behavioral responding to specific components of an aversive stimulus.