Evaluating the Effectiveness of Psychedelic-Assisted Therapy in Treating Alcohol Use Disorders: A Review
Alcoholism Treatment Quarterly May 2, 2025 DOI: 10.1080/07347324.2025.2500345 via Semantic Scholar
Summary
AI-generated from the abstractA narrative review of 71 studies on psychedelic-assisted therapy for alcohol use disorder (AUD) finds that psilocybin and LSD are associated with significant reductions in alcohol consumption, enhanced emotional regulation, and sustained mental health improvements over 6 to 32 weeks. A meta-analysis of six trials indicated that a single dose of LSD outperformed traditional medications like naltrexone and acamprosate in promoting long-term abstinence. The effects are thought to involve serotonin 2A receptor agonism and neuroplasticity in the prefrontal cortex. The review emphasizes psychedelic-assisted therapy as a promising alternative or adjunct to standard AUD treatments, especially when combined with behavioral therapies like Motivational Enhancement Therapy.
Study at a glance
| Characteristics | Narrative review Randomized Peer reviewed |
|---|---|
| Population | Individuals with alcohol use disorder |
| Keywords | Medicine Psychology |
| Key finding | Psilocybin and LSD are associated with significant reductions in alcohol consumption and improved long-term abstinence, with a single dose of LSD outperforming naltrexone and acamprosate in a meta-analysis of six trials. |
Abstract
ABSTRACT Background Alcohol Use Disorder (AUD) is a widespread condition with serious health, social, and economic impacts, often marked by relapse despite the availability of FDA-approved treatments. Recent studies suggest that psychedelic substances, such as psilocybin, Lysergic acid diethylamide (LSD), ayahuasca, etc. may offer novel therapeutic potential in treating AUD by modulating neurotransmission and promoting neuroplasticity. Ketamine is a dissociative psychedelic, and it works primarily by blocking NMDA receptors (a type of glutamate receptor in the brain) compared to Classic psychedelics (like LSD, psilocybin, mescaline) work mainly by activating serotonin 5-HT2A receptors hence ketamine was not the focus of this review. This narrative review aims to synthesize existing evidence on the effectiveness of psychedelic-assisted therapy for AUD. Methods A systematic literature search was conducted across PubMed and Google Scholar, yielding 186 articles. Following inclusion and exclusion criteria, 71 studies were selected for review, including randomized controlled trials, observational studies, and meta-analyses. These studies assessed the use of psychedelics (e.g. LSD, psilocybin) in individuals with AUD, focusing on therapeutic outcomes, neurobiological mechanisms, and safety profiles. Results Findings from clinical trials and observational studies suggest that psychedelic therapies, particularly those involving psilocybin and LSD, are associated with significant reductions in alcohol consumption, enhanced emotional regulation, and sustained improvements in mental health over follow-up periods ranging from 6 to 32 weeks. These effects are thought to be mediated by serotonin 2A receptor agonism, which promotes neuroplasticity in regions such as the prefrontal cortex, enhancing cognitive and emotional processes. A meta-analysis of six trials revealed that a single dose of LSD outperformed traditional pharmacotherapies like naltrexone and acamprosate in promoting long-term abstinence from alcohol. Conclusion This review emphasizes the potential of psychedelic-assisted therapy as a promising alternative or adjunctive treatment for AUD. Psychedelic substances, particularly when combined with behavioral therapies such as Motivational Enhancement Therapy (MET), show significant promise in reducing alcohol misuse and fostering long-term recovery. Despite the promising results, further research is needed to assess the safety, long-term efficacy, and optimal treatment protocols, particularly regarding patients with underlying psychiatric conditions. Future studies should focus on large-scale, controlled trials with neuroimaging and long-term follow-up to fully elucidate the neurobiological mechanisms underlying these therapeutic effects and to establish best practices for clinical use.