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Psychedelics Relax Priors and Reshape Orbitofrontal Dynamics

C. Delgado-Sallent, S. A. Ahmed, A. Khawaja-Lopez, B. S. Lee, R.a. Senne, B. B. Scott, S. Ramirez

bioRxiv Preprint Server September 18, 2025 preprint DOI: 10.1101/2025.09.18.677110 via bioRxiv

Summary

AI-generated from the abstract

Psychedelics like psilocybin and ketamine slow decision times and improve accuracy in mice performing a perceptual task. Behavioral modeling showed these changes stem from increased decision thresholds and a shift toward sensory-driven cognitive states. Whole-brain mapping revealed psychedelics selectively modulate a distributed decision-making network. Calcium imaging in the orbitofrontal cortex showed preserved decision-related selectivity but reduced neuronal correlations, indicating weakened top-down influence and relaxed prior expectations. These circuit-level findings support the REBUS model, suggesting psychedelics reconfigure brain dynamics to promote more deliberate, flexible, and sensory-driven decision policies.

Study at a glance

Characteristics Experimental study with behavioral modeling and neural recording
Population Mice
Interventions Psilocybin Ketamine
Key finding Psilocybin and ketamine slow decision times and improve accuracy by increasing decision thresholds and shifting mice into sensory-engaged cognitive states, providing circuit-level support for the REBUS model.

Abstract

Psychedelics such as psilocybin and ketamine are gaining attention as rapid-acting treatments for psychiatric disorders, yet the mechanisms by which they alter cognition remain unclear. A key hypothesis—the REBUS model—proposes that psychedelics relax high-level priors, allowing bottom-up sensory information to exert greater influence over perception and behavior. Here, we test this model in mice performing a free-response perceptual decision-making task that disambiguates prior-driven and sensory-driven decision strategies. Acute administration of psilocybin or ketamine significantly slowed decision times and improved accuracy. Behavioral modeling that combined drift diffusion and GLM-HMM frameworks revealed that these changes were mediated by increased decision thresholds and a marked shift into sensory-engaged cognitive states. Whole-brain c-Fos mapping identified a distributed decision-making network, with psychedelics selectively modulating cortical and subcortical nodes. Calcium imaging in the orbitofrontal cortex (OFC)—a key region for integrating priors and sensory inputs—revealed preserved decision-related selectivity under psychedelics, while exhibiting reduced neuronal correlations—population-level signatures of weakened top-down influence and relaxed priors. Together, these results provide circuit-level support for the REBUS model, showing that psychedelics reconfigure brain-wide and local dynamics to promote more deliberate, flexible, and sensory-driven decision policies.

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