Psilocybin triggers an activity-dependent rewiring of large-scale cortical networks

Psilocybin holds promise as a treatment for mental illnesses. One dose of psilocybin induces structural remodeling of dendritic spines in the medial frontal cortex in mice. The dendritic spines would be innervated by presynaptic neurons, but the sources of these inputs have not been identified. Here, using monosynaptic rabies tracing, we map the brain-wide distribution of inputs to frontal cortical pyramidal neurons. We discover that psilocybin's effect on connectivity is network specific, strengthening the routing of inputs from perceptual and medial regions (homolog of the default mode network) to subcortical targets while weakening inputs that are part of cortico-cortical recurrent loops. The pattern of synaptic reorganization depends on the drug-evoked spiking activity because silencing a presynaptic region during psilocybin administration disrupts the rewiring. Collectively, the results reveal the impact of psilocybin on the connectivity of large-scale cortical networks and demonstrate neural activity modulation as an approach to sculpt the psychedelic-evoked neural plasticity.

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Publication Details

Journal
Cell
Published
2025-12-05
DOI
https://doi.org/10.1016/j.cell.2025.11.009
Citations
6
Primary Topic
Psychedelics and Drug Studies
Type
article
Field-Weighted Citation Impact
13.84
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Psilocybin triggers an activity-dependent rewiring of large-scale cortical networks

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Cell
Psychedelics and Drug Studies
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article

Psilocybin triggers an activity-dependent rewiring of large-scale cortical networks

Tin Shing Hung, Hongkui Zeng, Quan Jiang, Alex C. Kwan, Ling-Xiao Shao, Annie-Kim Gilbert, Pasha A. Davoudian, H. M. Lai, Kevin T. Beier, Neil K. Savalia, Shenqin Yao, Guilian Tian, Jack D. Nothnagel
article en
6 citations

Abstract

Psilocybin holds promise as a treatment for mental illnesses. One dose of psilocybin induces structural remodeling of dendritic spines in the medial frontal cortex in mice. The dendritic spines would be innervated by presynaptic neurons, but the sources of these inputs have not been identified. Here, using monosynaptic rabies tracing, we map the brain-wide distribution of inputs to frontal cortical pyramidal neurons. We discover that psilocybin's effect on connectivity is network specific, strengthening the routing of inputs from perceptual and medial regions (homolog of the default mode network) to subcortical targets while weakening inputs that are part of cortico-cortical recurrent loops. The pattern of synaptic reorganization depends on the drug-evoked spiking activity because silencing a presynaptic region during psilocybin administration disrupts the rewiring. Collectively, the results reveal the impact of psilocybin on the connectivity of large-scale cortical networks and demonstrate neural activity modulation as an approach to sculpt the psychedelic-evoked neural plasticity.

CellVol. 189(2)
Allen Institute for Brain Science (US), Chinese University of Hong Kong (HK), University of California, Irvine (US), Cornell University (US), Yale University (US), Allen Institute (US)
Openalex Percentile: Top 1%
Psychedelics and Drug Studies
13.84
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