Psilocybin Enhances Cued Fear Extinction and Extinction Recall in Stress-Naïve, Acutely Stressed, and Chronically Stressed Mice
Noelle Cataldo, John A. Razidlo, Cody J. Wenthur
ACS Pharmacology & Translational Science September 11, 2025 DOI: 10.1021/acsptsci.5c00462 via OpenAlex
Summary
AI-generated from the abstractPsilocybin, a serotonergic psychedelic, enhanced fear extinction and improved extinction recall 24 hours later in male mice, regardless of whether they were stress-naïve or had been exposed to acute or chronic stress beforehand. Psilocybin transiently increased the stress hormone corticosterone in stress-naïve mice but not in previously stressed animals. The findings suggest psilocybin can promote fear extinction across different stress backgrounds, supporting its potential therapeutic relevance for disorders like PTSD where prior stress is a key factor.
Study at a glance
| Characteristics | Preclinical experimental study Peer reviewed |
|---|---|
| Population | Male mice |
| Intervention | Psilocybin |
| Citations | 2 |
| Key finding | Psilocybin enhanced fear extinction and promoted extinction recall in both stress-naïve and stressed male mice. |
Abstract
Serotonergic psychedelics have shown promise in clinical trials for treating an array of mental health disorders, including depression, anxiety, and post-traumatic stress disorder. Despite these findings, our understanding of how these drugs mechanistically exert their therapeutic effects remains incomplete. While researchers have regularly employed rodent preclinical models to assess such mechanisms, many of these findings arise from stress-naïve animals. Given that prior environmental stress is a critical component for the mental health disorders being studied in clinical trials of psychedelics, understanding the performance of these drugs in animals previously exposed to acute or chronic stress is of strong translational relevance. In this study, we examined the effects of psilocybin in male mice that were stress-naïve, as well as in those that underwent either single-prolonged stress (SPS) or chronic restraint stress (CRS). The effects of these treatments on corticosterone release, extinction of freezing behavior, and recall of extinction in Pavlovian fear conditioning were examined for each group. We observed that psilocybin challenge transiently increased serum corticosterone in stress-naïve mice relative to saline; however, this effect was not observed in SPS and CRS animals. Interestingly, psilocybin treatment enhanced fear extinction and promoted extinction recall 24 h later not only in stress-naïve animals but also in stressed animals. These findings indicate psilocybin's ability to acutely enhance fear extinction and promote enhanced extinction recall across animals with diverse environmental stress experiences prior to exposure.