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Context-dependent structurally informed effective connectivity under psilocybin

Matthew D. Greaves, Tamrin Barta, Leonardo Novelli, Devon Stoliker, Adeel Razi

bioRxiv (Cold Spring Harbor Laboratory) August 22, 2025 preprint DOI: 10.1101/2025.08.18.671000 via OpenAlex

Summary

AI-generated from the abstract

Psilocybin reorganizes directed influences between brain regions while preserving the underlying structural connectivity, according to fMRI data analyzed with a dynamic causal model. Across four contexts—rest, guided meditation, music listening, and movie viewing—effects converged on outgoing influences from the left hippocampus, a hub linking memory and association systems with the default-mode network and thalamus. The left-hippocampus-to-thalamus pathway showed a sign-reversed association with mystical-experience scores: downregulation during guided meditation and upregulation during music listening. Left-hippocampal efferents predicted individual differences in mystical-experience intensity in cross-validation, and a simpler measure of hippocampal signal variability showed modest associations.

Study at a glance

Characteristics Observational study with fMRI and dynamic causal modeling
Population Humans (fMRI data from a hippocampo-thalamo-cortical network)
Intervention Psilocybin
Topics Psilocybin
Keywords Context archaeology Hallucinogen Psychology Computer science
Key finding Psilocybin reorganizes directed inter-regional influences in a hippocampo–thalamo–cortical network while preserving structure-based scaling, and left-hippocampal efferents predict individual differences in mystical-experience intensity.

Abstract

Abstract The extent to which anatomical connectivity constrains pharmacologically altered brain dynamics remains poorly understood. Here, we combined psilocybin administration with a structurally informed effective-connectivity model to examine how structural connectivity shapes directed inter-regional influences across experiential contexts. Using dynamic causal modeling embedded in a hierarchical empirical Bayes framework, we analyzed fMRI data acquired from a hippocampo–thalamo–cortical network during rest, guided meditation, music listening and movie viewing. Across contexts, psilocybin reorganized directed interactions while preserving structure-based scaling. Effects converged on efferents (outgoing influences) from the left hippocampus—a hub interfacing mnemonic and associative systems with the default-mode network and thalamus. Notably, the left-hippocampus-to-thalamus pathway showed a sign-reversed association with mystical-experience scores (downregulation during guided meditation and upregulation during music listening). In model-based leave-one-out cross-validation, left-hippocampal efferents predicted individual differences in mystical-experience intensity. A minimal model-free benchmark (hippocampal signal variability) also showed modest associations with mystical experience. Together, these findings link context-specific, structurally informed effective connectivity to individual differences in the acute psychedelic experience, providing a mechanistic bridge between anatomy, neurodynamics, and phenomenology.

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