Psilocybin Decreases Preference for Large Rewards Accompanied by Increased Activity of Parvalbumin Neurons With Perineuronal Nets in the Medial Prefrontal Cortex.
Jenna Houff, Andrew Williams, Obie Allen, Barbara Gisabella, Harry Pantazopoulos, Alberto Del Arco
The European journal of neuroscience June 1, 2026 DOI: 10.1111/ejn.70574 via PubMed
Summary
AI-generated from the abstractA single dose of psilocybin reduced choices for larger, delayed rewards and increased the time rats took to choose them, measured 48 hours after administration. This effect was not tied to the delay length, indicating it did not alter impulsivity. Instead, the pattern suggests psilocybin decreased motivation for rewards. In the dorsomedial prefrontal cortex, psilocybin increased the density of neurons that were positive for perineuronal nets, parvalbumin, and c-Fos, pointing to heightened activity of a specific class of inhibitory interneurons. These findings propose that psilocybin lowers appetitive motivation by activating parvalbumin-positive interneurons surrounded by perineuronal nets in this brain region.
Study at a glance
| Characteristics | Randomized controlled trial Peer reviewed |
|---|---|
| Population | Male Long Evans rats |
| Intervention | Psilocybin |
| Duration | 48 hours after administration |
| Keywords | Impulsivity Long‐term Motivation Parvalbumin Perineuronal nets |
| Key finding | Psilocybin decreased large reward choices and increased latency to choose them 48 hours after administration, an effect attributed to reduced appetitive motivation rather than altered impulsivity, and was associated with increased activation of parvalbumin interneurons with perineuronal nets in the dorsomedial prefrontal cortex. |
Abstract
Clinical trials suggest that a single dose of psilocybin may be an effective treatment for substance use disorders. Choice impulsivity is a value-based decision-making bias that predicts drug-intake escalation and is commonly associated with substance use disorders. The dorsomedial prefrontal cortex regulates choice impulsivity and is enriched with 5-HT2A receptors that mediate effects of psilocybin. We hypothesized that psilocybin has long-term (≥ 48 h) effects on choice impulsivity in association with dorsomedial prefrontal cortex inhibitory interneurons with perineuronal nets (PNNs). Male Long Evans rats were trained in a delay discounting task where rats chose between delayed large rewards and immediate small rewards. Forty-eight hours after psilocybin or vehicle injections, delay discounting was assessed and rats' brains processed for microscopy analysis of extracellular matrix (PNNs) together with inhibitory parvalbumin (PV) interneurons and c-Fos as a marker of neuronal activity. Psilocybin acutely increased head-twitch responses. Psilocybin decreased large reward choices and increased the latency to large reward choices 48 h after administration. These effects were independent of delay and therefore not consistent with changes in impulsivity. Psilocybin also increased the density of triple-labelled neurons (PNN + PV + cFos) in the dorsomedial prefrontal cortex. These results suggest that psilocybin decreases appetitive motivation through the increased activation of PV interneurons with PNNs in the dorsomedial prefrontal cortex.