Sex-specific increased reactivity of the PVT and prolonged PVT→CeA circuit engagement following psilocin administration
The psychedelic psilocybin has shown therapeutic potential, yet underlying neural mechanisms remain poorly understood. We investigated the impact of psilocin-the active metabolite of psilocybin-on basal activity and reactivity within the paraventricular nucleus of the thalamus (PVT) and PVT projections to central amygdala (CeA) in rats. Psilocin administration increased PVT c-Fos expression and selectively engaged PVT→CeA neurons in females, but not males. Psilocin enhanced PVT reactivity to an aversive air-puff stimulus, with effects primarily driven by passive responders. In PVT→CeA neurons, psilocin prevented time-dependent reductions in stimulus-evoked activity and maintained reactivity across timepoints in females but not males. The sustained engagement of PVT→CeA circuitry was driven by active responders. These findings identify sex-specific modulation of thalamic-limbic circuitry and behavior by psilocin, implicating PVT→CeA circuitry in the neural and behavioral effects of psychedelic compounds, advancing our understanding of how psychedelics modulate emotional brain circuits to further inform potential therapeutic mechanisms.
Authors
- Sema G. Quadir
- Melissa A. Herman (ORCID: https://orcid.org/0000-0002-7260-3439)
- C. S. Rollison
- M. W. High
- D. P. Effinger
- J. L. Hoffman
- M. Echeveste Sanchez
- D. Toedt (ORCID: https://orcid.org/0009-0009-6824-9201)
- C. W. Hodge
Institutions
- University of North Carolina at Chapel Hill (US)
- University of North Carolina Health Care (US)
- University of Colorado Anschutz Medical Campus (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-04-10
- DOI
- https://doi.org/10.1038/s41467-026-71481-1
- Primary Topic
- Psychedelics and Drug Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Alliance for Research on Schizophrenia and Depression
- National Institute on Alcohol Abuse and Alcoholism
- National Institute of General Medical Sciences