Cannabidiol as a Novel Candidate Alcohol Use Disorder Pharmacotherapy: A Systematic Review

被引:59
|
作者
Turna, Jasmine [1 ,2 ,3 ]
Syan, Sabrina K. [2 ,3 ,4 ,5 ]
Frey, Benicio N. [5 ,6 ,7 ]
Rush, Brian [8 ,9 ]
Costello, Mary Jean [9 ]
Weiss, Mark [10 ]
MacKillop, James [1 ,2 ,3 ,4 ,5 ,9 ]
机构
[1] McMaster Univ, Michael G DeGroote Ctr Med Cannabis Res, Hamilton, ON, Canada
[2] St Josephs Healthcare Hamilton, Hamilton, ON, Canada
[3] McMaster Univ, Peter Boris Ctr Addict Res, Hamilton, ON, Canada
[4] McMaster Univ, Dept Psychol Neurosci & Behav, Hamilton, ON, Canada
[5] McMaster Univ, Dept Psychiat & Behav Neurosci, Hamilton, ON, Canada
[6] St Josephs Healthcare Hamilton, Mood Disorders Program, Hamilton, ON, Canada
[7] St Josephs Healthcare Hamilton, Womens Hlth Concerns Clin, Hamilton, ON, Canada
[8] Ctr Addict & Mental Hlth, Toronto, ON, Canada
[9] Homewood Res Inst, Guelph, ON, Canada
[10] Homewood Hlth Ctr, Addict Med Serv, Guelph, ON, Canada
来源
关键词
Cannabidiol; Alcohol Use Disorder; CBD; Alcohol; Pharmacotherapy; PLACEBO-CONTROLLED TRIAL; VOLUNTARY ETHANOL INTAKE; DOUBLE-BLIND; ALLOSTERIC MODULATOR; NATURAL RESOLUTION; RECEPTOR AGONISTS; OXIDATIVE STRESS; DEPENDENCE; LEVETIRACETAM; ANTAGONIST;
D O I
10.1111/acer.13964
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
There is substantial interest in the therapeutic potential of cannabidiol (CBD), a nonpsychoactive cannabinoid found in plants of the genus Cannabis. The goal of the current systematic review was to characterize the existing literature on this topic and to evaluate the credibility of CBD as a candidate pharmacotherapy for alcohol use disorder (AUD). Using a comprehensive search strategy, 303 unique potential articles were identified and 12 ultimately met criteria for inclusion (8 using rodent models, 3 using healthy adult volunteers, and 1 using cell culture). In both rodent and cell culture models, CBD was found to exert a neuroprotective effect against adverse alcohol consequences on the hippocampus. In rodent models, CBD was found to attenuate alcohol-induced hepatotoxicity, specifically, alcohol-induced steatosis. Finally, findings from preclinical rodent models also indicate that CBD attenuates cue-elicited and stress-elicited alcohol seeking, alcohol self-administration, withdrawal-induced convulsions, and impulsive discounting of delayed rewards. In human studies, CBD was well tolerated and did not interact with the subjective effects of alcohol. Collectively, given its favorable effects on alcohol-related harms and addiction phenotypes in preclinical models, CBD appears to have promise as a candidate AUD pharmacotherapy. This is further bolstered by the absence of abuse liability and its general tolerability. A clear limitation to the literature is the paucity of human investigations. Human preclinical and clinical studies are needed to determine whether these positive effects in model systems substantively translate into clinically relevant outcomes.
引用
收藏
页码:550 / 563
页数:14
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