# Psilocybin effects on brain functional connectivity: a systematic review of fMRI studies

**Authors:** Àlvar Farré-Colomés, Olga Rublinetska, Óscar Soto-Angona

PMC · DOI: 10.1007/s44192-026-00384-w · 2026-03-19

## TL;DR

This review summarizes fMRI studies on how psilocybin affects brain connectivity, highlighting gaps in research and inconsistent methods.

## Contribution

The paper systematically compiles fMRI evidence on psilocybin's effects, emphasizing the need for standardized research methods.

## Key findings

- Most studies focused on the amygdala, anterior cingulate cortex, and prefrontal cortex.
- High dropout rates and limited follow-up timepoints were common in the reviewed studies.
- Inconsistent methods and designs were identified across the current literature.

## Abstract

Psilocybin-assisted therapies are innovative therapeutic approaches, particularly in the treatment of depression. However, there are sparse studies providing functional magnetic resonance imaging (fMRI) evidence elucidating the underlying biological mechanisms that support clinical outcomes. This review aims to comprehensively gather all the evidence reported in psilocybin studies using fMRI techniques. Independent extraction of articles was conducted by 2 authors using predefined data fields. 20 unique datasets were identified, with 5 including participants diagnosed with depression. Dropout rates were found to be high, and follow-up scanning timepoints were lacking in most of the studies. Most research has focused on the amygdala, the anterior cingulate cortex and the prefrontal cortex, as key regions involved in the effects of psilocybin. However, the current literature exhibits inconsistency in methods and designs. Further research is necessary to better define psilocybin’s impact on the human brain and its potential to enhance psychotherapy outcomes.

## Linked entities

- **Chemicals:** psilocybin (PubChem CID 10624)
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Diseases:** TRMD (MESH:D061218), psychiatric (MESH:D001523), addiction (MESH:D019966), pain (MESH:D010146), cardiovascular disease (MESH:D002318), addiction disorders (MESH:D000437), Depression (MESH:D003866), claustrophobia (MESH:D010698), -resistant major depression (MESH:D003865), nicotine dependence (MESH:D014029), Chronic cluster headache (MESH:D003027), head injury (MESH:D006259), Anxiety (MESH:D001007), consciousness (MESH:D003244), anorexia (MESH:D000855)
- **Chemicals:** psilocin (MESH:C009105), escitalopram (MESH:D000089983), FC (-), Psi (MESH:D011562), DMT (MESH:D004130), LSD (MESH:D008238), mescaline (MESH:D008635)
- **Species:** Agaricus bisporus (common mushroom, species) [taxon 5341], Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13003063/full.md

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Source: https://tomesphere.com/paper/PMC13003063