Cargando…
Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants
Mescaline, lysergic acid diethylamide (LSD), and psilocybin are classic serotonergic psychedelics. A valid, direct comparison of the effects of these substances is lacking. The main goal of the present study was to investigate potential pharmacological, physiological and phenomenological differences...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517157/ https://www.ncbi.nlm.nih.gov/pubmed/37231080 http://dx.doi.org/10.1038/s41386-023-01607-2 |
_version_ | 1785109268017446912 |
---|---|
author | Ley, Laura Holze, Friederike Arikci, Denis Becker, Anna M. Straumann, Isabelle Klaiber, Aaron Coviello, Fabio Dierbach, Sophie Thomann, Jan Duthaler, Urs Luethi, Dino Varghese, Nimmy Eckert, Anne Liechti, Matthias E. |
author_facet | Ley, Laura Holze, Friederike Arikci, Denis Becker, Anna M. Straumann, Isabelle Klaiber, Aaron Coviello, Fabio Dierbach, Sophie Thomann, Jan Duthaler, Urs Luethi, Dino Varghese, Nimmy Eckert, Anne Liechti, Matthias E. |
author_sort | Ley, Laura |
collection | PubMed |
description | Mescaline, lysergic acid diethylamide (LSD), and psilocybin are classic serotonergic psychedelics. A valid, direct comparison of the effects of these substances is lacking. The main goal of the present study was to investigate potential pharmacological, physiological and phenomenological differences at psychoactive-equivalent doses of mescaline, LSD, and psilocybin. The present study used a randomized, double-blind, placebo-controlled, cross-over design to compare the acute subjective effects, autonomic effects, and pharmacokinetics of typically used, moderate to high doses of mescaline (300 and 500 mg), LSD (100 µg), and psilocybin (20 mg) in 32 healthy participants. A mescaline dose of 300 mg was used in the first 16 participants and 500 mg was used in the subsequent 16 participants. Acute subjective effects of 500 mg mescaline, LSD, and psilocybin were comparable across various psychometric scales. Autonomic effects of 500 mg mescaline, LSD, and psilocybin were moderate, with psilocybin causing a higher increase in diastolic blood pressure compared with LSD, and LSD showing a trend toward an increase in heart rate compared with psilocybin. The tolerability of mescaline, LSD, and psilocybin was comparable, with mescaline at both doses inducing slightly more subacute adverse effects (12–24 h) than LSD and psilocybin. Clear distinctions were seen in the duration of action between the three substances. Mescaline had the longest effect duration (mean: 11.1 h), followed by LSD (mean: 8.2 h), and psilocybin (mean: 4.9 h). Plasma elimination half-lives of mescaline and LSD were similar (approximately 3.5 h). The longer effect duration of mescaline compared with LSD was due to the longer time to reach maximal plasma concentrations and related peak effects. Mescaline and LSD, but not psilocybin, enhanced circulating oxytocin. None of the substances altered plasma brain-derived neurotrophic factor concentrations. In conclusion, the present study found no evidence of qualitative differences in altered states of consciousness that were induced by equally strong doses of mescaline, LSD, and psilocybin. The results indicate that any differences in the pharmacological profiles of mescaline, LSD, and psilocybin do not translate into relevant differences in the subjective experience. ClinicalTrials.gov identifier: NCT04227756. |
format | Online Article Text |
id | pubmed-10517157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-105171572023-09-24 Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants Ley, Laura Holze, Friederike Arikci, Denis Becker, Anna M. Straumann, Isabelle Klaiber, Aaron Coviello, Fabio Dierbach, Sophie Thomann, Jan Duthaler, Urs Luethi, Dino Varghese, Nimmy Eckert, Anne Liechti, Matthias E. Neuropsychopharmacology Article Mescaline, lysergic acid diethylamide (LSD), and psilocybin are classic serotonergic psychedelics. A valid, direct comparison of the effects of these substances is lacking. The main goal of the present study was to investigate potential pharmacological, physiological and phenomenological differences at psychoactive-equivalent doses of mescaline, LSD, and psilocybin. The present study used a randomized, double-blind, placebo-controlled, cross-over design to compare the acute subjective effects, autonomic effects, and pharmacokinetics of typically used, moderate to high doses of mescaline (300 and 500 mg), LSD (100 µg), and psilocybin (20 mg) in 32 healthy participants. A mescaline dose of 300 mg was used in the first 16 participants and 500 mg was used in the subsequent 16 participants. Acute subjective effects of 500 mg mescaline, LSD, and psilocybin were comparable across various psychometric scales. Autonomic effects of 500 mg mescaline, LSD, and psilocybin were moderate, with psilocybin causing a higher increase in diastolic blood pressure compared with LSD, and LSD showing a trend toward an increase in heart rate compared with psilocybin. The tolerability of mescaline, LSD, and psilocybin was comparable, with mescaline at both doses inducing slightly more subacute adverse effects (12–24 h) than LSD and psilocybin. Clear distinctions were seen in the duration of action between the three substances. Mescaline had the longest effect duration (mean: 11.1 h), followed by LSD (mean: 8.2 h), and psilocybin (mean: 4.9 h). Plasma elimination half-lives of mescaline and LSD were similar (approximately 3.5 h). The longer effect duration of mescaline compared with LSD was due to the longer time to reach maximal plasma concentrations and related peak effects. Mescaline and LSD, but not psilocybin, enhanced circulating oxytocin. None of the substances altered plasma brain-derived neurotrophic factor concentrations. In conclusion, the present study found no evidence of qualitative differences in altered states of consciousness that were induced by equally strong doses of mescaline, LSD, and psilocybin. The results indicate that any differences in the pharmacological profiles of mescaline, LSD, and psilocybin do not translate into relevant differences in the subjective experience. ClinicalTrials.gov identifier: NCT04227756. Springer International Publishing 2023-05-25 2023-10 /pmc/articles/PMC10517157/ /pubmed/37231080 http://dx.doi.org/10.1038/s41386-023-01607-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ley, Laura Holze, Friederike Arikci, Denis Becker, Anna M. Straumann, Isabelle Klaiber, Aaron Coviello, Fabio Dierbach, Sophie Thomann, Jan Duthaler, Urs Luethi, Dino Varghese, Nimmy Eckert, Anne Liechti, Matthias E. Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title | Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title_full | Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title_fullStr | Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title_full_unstemmed | Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title_short | Comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
title_sort | comparative acute effects of mescaline, lysergic acid diethylamide, and psilocybin in a randomized, double-blind, placebo-controlled cross-over study in healthy participants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517157/ https://www.ncbi.nlm.nih.gov/pubmed/37231080 http://dx.doi.org/10.1038/s41386-023-01607-2 |
work_keys_str_mv | AT leylaura comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT holzefriederike comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT arikcidenis comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT beckerannam comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT straumannisabelle comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT klaiberaaron comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT coviellofabio comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT dierbachsophie comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT thomannjan comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT duthalerurs comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT luethidino comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT varghesenimmy comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT eckertanne comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants AT liechtimatthiase comparativeacuteeffectsofmescalinelysergicaciddiethylamideandpsilocybininarandomizeddoubleblindplacebocontrolledcrossoverstudyinhealthyparticipants |