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Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios

As countries adopt more permissive cannabis policies, it is increasingly important to identify strategies that can reduce the harmful effects of cannabis use. This study aimed to determine if increasing the CBD content of cannabis can reduce its harmful effects. Forty-six healthy, infrequent cannabi...

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Autores principales: Englund, Amir, Oliver, Dominic, Chesney, Edward, Chester, Lucy, Wilson, Jack, Sovi, Simina, De Micheli, Andrea, Hodsoll, John, Fusar-Poli, Paolo, Strang, John, Murray, Robin M., Freeman, Tom P., McGuire, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156730/
https://www.ncbi.nlm.nih.gov/pubmed/36380220
http://dx.doi.org/10.1038/s41386-022-01478-z
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author Englund, Amir
Oliver, Dominic
Chesney, Edward
Chester, Lucy
Wilson, Jack
Sovi, Simina
De Micheli, Andrea
Hodsoll, John
Fusar-Poli, Paolo
Strang, John
Murray, Robin M.
Freeman, Tom P.
McGuire, Philip
author_facet Englund, Amir
Oliver, Dominic
Chesney, Edward
Chester, Lucy
Wilson, Jack
Sovi, Simina
De Micheli, Andrea
Hodsoll, John
Fusar-Poli, Paolo
Strang, John
Murray, Robin M.
Freeman, Tom P.
McGuire, Philip
author_sort Englund, Amir
collection PubMed
description As countries adopt more permissive cannabis policies, it is increasingly important to identify strategies that can reduce the harmful effects of cannabis use. This study aimed to determine if increasing the CBD content of cannabis can reduce its harmful effects. Forty-six healthy, infrequent cannabis users participated in a double-blind, within-subject, randomised trial of cannabis preparations varying in CBD content. There was an initial baseline visit followed by four drug administration visits, in which participants inhaled vaporised cannabis containing 10 mg THC and either 0 mg (0:1 CBD:THC), 10 mg (1:1), 20 mg (2:1), or 30 mg (3:1) CBD, in a randomised, counter-balanced order. The primary outcome was change in delayed verbal recall on the Hopkins Verbal Learning Task. Secondary outcomes included change in severity of psychotic symptoms (e.g., Positive and Negative Syndrome Scale [PANSS] positive subscale), plus further cognitive, subjective, pleasurable, pharmacological and physiological effects. Serial plasma concentrations of THC and CBD were measured. THC (0:1) was associated with impaired delayed verbal recall (t(45) = 3.399, d = 0.50, p = 0.001) and induced positive psychotic symptoms on the PANSS (t(45) = −4.709, d = 0.69, p = 2.41 × 10(–5)). These effects were not significantly modulated by any dose of CBD. Furthermore, there was no evidence of CBD modulating the effects of THC on other cognitive, psychotic, subjective, pleasurable, and physiological measures. There was a dose-response relationship between CBD dose and plasma CBD concentration, with no effect on plasma THC concentrations. At CBD:THC ratios most common in medicinal and recreational cannabis products, we found no evidence that CBD protects against the acute adverse effects of cannabis. This should be considered in health policy and safety decisions about medicinal and recreational cannabis.
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spelling pubmed-101567302023-05-05 Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios Englund, Amir Oliver, Dominic Chesney, Edward Chester, Lucy Wilson, Jack Sovi, Simina De Micheli, Andrea Hodsoll, John Fusar-Poli, Paolo Strang, John Murray, Robin M. Freeman, Tom P. McGuire, Philip Neuropsychopharmacology Article As countries adopt more permissive cannabis policies, it is increasingly important to identify strategies that can reduce the harmful effects of cannabis use. This study aimed to determine if increasing the CBD content of cannabis can reduce its harmful effects. Forty-six healthy, infrequent cannabis users participated in a double-blind, within-subject, randomised trial of cannabis preparations varying in CBD content. There was an initial baseline visit followed by four drug administration visits, in which participants inhaled vaporised cannabis containing 10 mg THC and either 0 mg (0:1 CBD:THC), 10 mg (1:1), 20 mg (2:1), or 30 mg (3:1) CBD, in a randomised, counter-balanced order. The primary outcome was change in delayed verbal recall on the Hopkins Verbal Learning Task. Secondary outcomes included change in severity of psychotic symptoms (e.g., Positive and Negative Syndrome Scale [PANSS] positive subscale), plus further cognitive, subjective, pleasurable, pharmacological and physiological effects. Serial plasma concentrations of THC and CBD were measured. THC (0:1) was associated with impaired delayed verbal recall (t(45) = 3.399, d = 0.50, p = 0.001) and induced positive psychotic symptoms on the PANSS (t(45) = −4.709, d = 0.69, p = 2.41 × 10(–5)). These effects were not significantly modulated by any dose of CBD. Furthermore, there was no evidence of CBD modulating the effects of THC on other cognitive, psychotic, subjective, pleasurable, and physiological measures. There was a dose-response relationship between CBD dose and plasma CBD concentration, with no effect on plasma THC concentrations. At CBD:THC ratios most common in medicinal and recreational cannabis products, we found no evidence that CBD protects against the acute adverse effects of cannabis. This should be considered in health policy and safety decisions about medicinal and recreational cannabis. Springer International Publishing 2022-11-16 2023-05 /pmc/articles/PMC10156730/ /pubmed/36380220 http://dx.doi.org/10.1038/s41386-022-01478-z Text en © The Author(s) 2022 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
Englund, Amir
Oliver, Dominic
Chesney, Edward
Chester, Lucy
Wilson, Jack
Sovi, Simina
De Micheli, Andrea
Hodsoll, John
Fusar-Poli, Paolo
Strang, John
Murray, Robin M.
Freeman, Tom P.
McGuire, Philip
Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title_full Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title_fullStr Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title_full_unstemmed Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title_short Does cannabidiol make cannabis safer? A randomised, double-blind, cross-over trial of cannabis with four different CBD:THC ratios
title_sort does cannabidiol make cannabis safer? a randomised, double-blind, cross-over trial of cannabis with four different cbd:thc ratios
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156730/
https://www.ncbi.nlm.nih.gov/pubmed/36380220
http://dx.doi.org/10.1038/s41386-022-01478-z
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