Journal of Psychopharmacology
June 19, 2013
Rl Carhart-Harris, Stefan Brugger, Dj Nutt et al.
43 citations
Five drugs—cannabis, psilocybin, amphetamine, ketamine, and alcohol—were compared for how well they model psychiatric symptoms. Mental health professionals rated how specific certain experiences were to symptom clusters like depression or psychosis. People with personal drug experience then reported how reliably each drug produced those experiences. No experiences were specific to negative or cognitive psychotic symptoms over depression. Psilocybin best modeled positive psychotic symptoms, while acute alcohol and amphetamine best modeled mania. These findings challenge current assumptions about drug models and point to an understudied area needing more research.
Drug Science Policy and Law
January 1, 2020
Jec Anthony, Adam Winstock, Ja Ferris et al.
9 citations
People with color blindness have reported improvements after using psychedelic drugs like LSD and psilocybin. In the Global Drugs Survey 2017, 47 respondents provided useful descriptions, and 23 reported improved color blindness. Some said the effect lasted from days to years. The improvement may result from new visual experiences (photisms) during the psychedelic state linking with existing color concepts, possibly due to enhanced connections between visual and language brain areas. This preliminary data suggests further investigation is warranted.
Psychiatry and Clinical Neurosciences
February 26, 2026
Kengo Yonezawa, M. Hirata, Hiroaki Takano et al.
1 citation
Psilocybin, a classic psychedelic compound, is being reexamined as a treatment for psychiatric disorders after decades of legal restrictions. Clinical trials report therapeutic effects for major depressive disorder, depressive symptoms in life-threatening illnesses, and some substance use disorders, with phase III trials for depression underway. Short-term side effects are generally mild and transient, but long-term effects need investigation. Neuroimaging research, mainly using MRI and EEG, is limited and focused on MDD, though ongoing trials include broader studies. Regulatory frameworks vary; controlled use is permitted in Switzerland, parts of the US, Canada, and Australia. Challenges remain, including the need for larger blinded trials and standardized protocols.
October 14, 2024
Terence J. Lyons, Merle Spriggs, Leevi Kerkelä et al.
preprint
A single high dose of psilocybin (25 mg) produced lasting functional and anatomical brain changes in healthy, psychedelic-naive adults, detected from one hour to one month later. Diffusion imaging showed decreased axial diffusivity in prefrontal-subcortical tracts, correlating with reduced brain network modularity, which in turn correlated with improved well-being. Increased cortical signal entropy shortly after dosing predicted better psychological well-being at one month, with next-day psychological insight mediating this relationship. No such effects occurred with a 1 mg placebo dose. Cognitive flexibility, psychological insight, and well-being also increased at one month.