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Psilocybin Attenuates Cortical Representations of Aversion in the Mouse Auditory Cortex.

James D. Johnson, Runyi Tian, Yasaman Etemadi, Zheng Li

bioRxiv : the preprint server for biology March 27, 2026 DOI: 10.64898/2026.03.26.714498 via PubMed

Summary

AI-generated from the abstract

Psilocybin preferentially dampens well-consolidated aversive sensory representations in the auditory cortex, rather than fresh associations, without broadly affecting auditory processing or new aversive learning. Using longitudinal two-photon calcium imaging in awake mice, psilocybin selectively reduced responses to aversive stimuli and earlier-established aversive-associated tones, while reward responses and responses to newly aversive-associated tones remained unaffected. At the population level, psilocybin acutely increased coordination across tone-responsive neurons, then later reduced it selectively among neurons encoding the aversive-associated tone. These results suggest psilocybin reshapes sensory representations of learned valence associations, potentially explaining its benefits in affective and trauma-related disorders.

Study at a glance

Characteristics Longitudinal two-photon calcium imaging study Peer reviewed
Population Awake C57BL/6 mice
Intervention Psilocybin
Topics Psilocybin
Keywords Auditory cortex Aversive Psychedelic Valence
Key finding Psilocybin selectively reduces responses to aversive stimuli and earlier-established aversive-associated tones in auditory cortex without affecting reward responses or new aversive learning.

Abstract

Psilocybin can produce sustained benefits in affective and trauma-related disorders, yet if and how it reshapes sensory representations of learned valence associations remains largely unclear. To address this, we used longitudinal two-photon calcium imaging in awake C57BL/6 mice to examine how psilocybin modulates layer 2/3 auditory cortex activity at single-cell and population levels. Evoked responses were measured for tones with or without prior associations with valenced stimuli, as well as for the valenced stimuli themselves. Most responsive neurons were selective for tones alone, while distinct subsets responded exclusively to reward or aversive stimuli, and a smaller population encoded both. Psilocybin selectively reduced responses to aversive stimuli and earlier-established aversive-associated tones, without affecting aversive association, reward responses, or responses to newly aversive-associated tones. At the population level, psilocybin acutely increased coordination across tone-responsive neurons, while later reducing it selectively among neurons encoding the aversive-associated tone. These results demonstrate that psilocybin preferentially dampens well consolidated aversive sensory representations in auditory cortex, rather than fresh associations, without broadly affecting auditory processing or new aversive learning.

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