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R L Carhart-Harris

Centres for Neuropsychopharmacology & Psychedelic Research, Division of Psychiatry, Department of Brain Sciences, Imperial College London, London, UK.

3 papers in the library · 124 citations · publishing 2019-2026

Papers

Replication and extension of a model predicting response to psilocybin.

Psychopharmacology November 1, 2019 Suzanne L Russ, R L Carhart-Harris, G Maruyama et al. 75 citations

A state of surrender before taking psilocybin predicts a mystical experience, while a state of preoccupation predicts an adverse experience. These mental states explain substantial variation in how people respond to the drug. The study replicated an earlier model using retrospective data from 183 individuals who had self-administered psilocybin in the past year. Mystical experiences were linked to long-term positive change. Recognizing and cultivating a surrendering mindset before ingestion could improve the therapeutic use of psilocybin in clinical settings.

Psilocybin and Other Classic Psychedelics in Depression.

Current topics in behavioral neurosciences January 1, 2024 D J Nutt, J M Peill, B Weiss et al. 30 citations

Psychedelic drugs that activate the 5-HT2A receptor, such as psilocybin and DMT, produce dose-related psychological effects including hallucinations, out-of-body experiences, emotional breakthroughs, and mystical-type experiences. When combined with psychological support, these substances can rapidly improve mood in people with depression, with benefits lasting months. The therapeutic effects may stem from increased brain entropy that disrupts fixed negative thinking, enhanced cognitive flexibility after treatment, and changes in self-referential psychological processes. The brain mechanisms underlying serotonergic psychedelics likely differ from those of classical serotonin reuptake-blocking antidepressants.

Human brain changes after first psilocybin use.

Nature communications May 5, 2026 T Lyons, M Spriggs, L Kerkelä et al. 19 citations

A single high dose of psilocybin (25 mg) in 28 healthy, psychedelic-naive participants produced anatomical and functional brain changes lasting from one hour to one month. At one month, participants showed increased cognitive flexibility, psychological insight, and well-being. Diffusion tensor imaging revealed decreased axial diffusivity in prefrontal-subcortical tracts, correlating with reduced brain network modularity. Decreased modularity negatively correlated with increased well-being, consistent with depression findings. Increased cortical signal entropy one to two hours after dosing predicted improved well-being at one month, mediated by next-day psychological insight. No effects occurred with a 1 mg placebo dose.