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Effective connectivity of the human claustrum: Triple networks, subcortical circuits, and psychedelic modulation

Navid Shams Masjedi, Adeel Razi

bioRxiv (Cold Spring Harbor Laboratory) September 12, 2025 preprint DOI: 10.1101/2025.09.07.674759 via OpenAlex

Summary

AI-generated from the abstract

The claustrum, a brain region with extensive connections to both cortical and subcortical areas, may help synchronize brain networks. Psychedelics like psilocybin appear to disrupt this synchrony by altering claustral signaling. Using brain scans from the Human Connectome Project and PsiConnect datasets, this work provides the first in vivo description of how the claustrum communicates with key brain networks in humans, both at rest and under psilocybin. The claustrum showed widespread bidirectional connections and a strong inhibitory influence on target regions. Psilocybin increased this inhibition on cortical networks while reducing it on subcortical areas, partly linked to subjective psychedelic effects, supporting a role for claustro-cortical inhibition in regulating network synchrony.

Study at a glance

Characteristics Observational cohort with experimental drug intervention
Population Humans
Intervention Psilocybin
Key finding Psilocybin enhances claustral inhibition of cortical networks while disinhibiting subcortical areas, partially associated with subjective psychedelic effects.

Abstract

Abstract Decades of cross-species research highlight the claustrums extensive bidirectional connectivity with cortical and subcortical regions, implicating it in higher-order cognitive processes requiring synchronized brain states. Psychedelics may disrupt this synchrony by modulating claustro-cortical signaling, reflected by the dissolution of cortical network signatures. Using spectral dynamic causal modeling on resting-state fMRI data from the Human Connectome Project and PsiConnect datasets at 7T and 3T, we provide the first in vivo characterization of claustral effective connectivity with triple networks and subcortical regions in humans, both at rest and under the influence of psilocybin. Claustra displayed widespread bidirectional effective connectivity and a strong inhibitory influence on all target regions. Psilocybin enhanced claustral inhibition of cortical networks while disinhibiting subcortical areas, partially associated with psychedelic subjective effect scores. These findings are consistent with cellular and functional cross-species data, supporting the proposed mechanism of claustro-cortical inhibition in regulating network synchrony, while extending this influence to the subcortex, and revealing hierarchical and hemispheric asymmetries in claustral signaling modulation under psilocybin.

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