Journal of substance use and addiction treatment
August 1, 2025
Reinhard Janssen-Aguilar, Shakila Meshkat, Ilya Demchenko et al.
12 citations
Ketamine may offer short-term benefits for treating substance use disorders, including alcohol, cocaine, opioid, and cannabis use disorders. In alcohol use disorder, it reduced withdrawal symptoms and the need for benzodiazepines. For cocaine use disorder, it decreased craving and increased abstinence rates. In opioid use disorder, high-dose ketamine combined with psychotherapy improved abstinence and reduced craving. For cannabis use disorder, it reduced weekly use and increased confidence in abstinence. However, the evidence is limited by small sample sizes and a lack of randomized trials. Larger, well-controlled studies are needed to determine optimal dosing, mechanisms, long-term efficacy, and risks before broader clinical use can be recommended.
Neuroscience and biobehavioral reviews
June 1, 2025
Shakila Meshkat, Gunjan Malik, Richard J Zeifman et al.
11 citations
Psilocybin-assisted psychotherapy may reduce alcohol consumption and help with smoking cessation, especially for alcohol and tobacco use disorders. In a systematic review of 16 published studies, most focused on alcohol or tobacco use, and over half used psilocybin combined with psychotherapy. Doses ranged from microdosing to 20–40 mg per 70 kg. Alcohol use disorder studies reported fewer heavy drinking days and higher abstinence rates, with brain scans showing normalized activity. Tobacco use disorder studies found high smoking abstinence rates, with mystical experiences predicting long-term success. Findings for other substance use disorders were mixed. The evidence is preliminary; larger clinical trials are needed.
Expert review of clinical pharmacology
January 1, 2023
Luke J Ney, Wole Akosile, Chris Davey et al.
8 citations
Preclinical and experimental research suggests medicinal cannabis may help treat posttraumatic stress disorder, but integrating it into routine clinical therapies poses clinical, practical, and safety challenges, especially when combined with trauma-focused psychotherapy. Key issues include dose timing and titration, addiction potential, product formulation, windows of intervention, and route of administration. Exposure therapy for PTSD involves recalling intense emotions, and the interaction between cannabis use and reliving trauma memories requires exploration for patient safety and therapeutic outcomes.
Progress in neuro-psychopharmacology & biological psychiatry
July 14, 2025
Zoe Plummer, Josh Allen, Justin Brand et al.
4 citations
Traumatic brain injury (TBI) causes neuroinflammation, oxidative stress, impaired neuroplasticity, neurotransmitter imbalances, and cell death, leading to neurological and psychiatric disorders. The serotonergic psychedelics psilocybin and 5-MeO-DMT may help treat TBI by promoting neuroplasticity, reducing inflammation, and protecting neurons. Psilocybin acts through 5-HT1A, 5-HT2A, and neurotrophic TrkB receptors, while 5-MeO-DMT targets sigma-1 receptors with neuroprotective properties. Preclinical and clinical research suggests these compounds can alleviate cognitive and affective dysfunction and neuroinflammation after TBI. The review critically examines safety, dosing, and clinical challenges, highlighting the potential of these psychedelics as adjunctive treatments in neurorehabilitation.
Journal of Psychoactive Drugs
January 29, 2025
Carrie Cuttler, Amanda Stueber, Jonathan Simone et al.
3 citations
An online survey of 1,486 U.S. adults (average age 29.58, 67.1% male) examined patterns of psychedelic use. Respondents most often used MDMA, LSD, DMT, and psilocybin, primarily by oral administration and for recreational purposes. The most common acute effects were hallucinations, increased heart rate, positive mood, and visual tracers; residual effects included headaches, dry mouth, nausea, hallucinations, and anxiety. Distress about negative mood, vomiting, and nausea during acute effects was low on average. These findings can inform clinical trials and policy as psychedelic legality and accessibility evolve.
Psychopharmacology
February 1, 2026
Ana Deutsch, Connor J Haggarty, Gavin N Petrie et al.
1 citation
A single oral dose of methamphetamine (20 mg) reduced blood levels of the endocannabinoid 2-AG in healthy adults, while MDMA (100 mg) did not. Neither drug affected anandamide (AEA) levels. Under placebo, higher AEA concentrations were linked to disliking the drug effects, suggesting a connection between AEA and negative expectations. These findings show how stimulants act on the endocannabinoid system and may inform treatments for substance use disorders.