Cannabidiol alters psychophysiological, craving and anxiety responses in an alcohol cue reactivity task: A cross-over randomized controlled trial

IF 3 Q2 SUBSTANCE ABUSE
Tristan Hurzeler, Warren Logge, Joshua Watt, Ian S. McGregor, Anastasia Suraev, Paul S. Haber, Kirsten C. Morley
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Abstract

Background

Preclinical studies have demonstrated that cannabidiol (CBD) reduces alcohol-seeking behaviors and may have potential for managing alcohol use disorder (AUD). In this study, we examined the effects of CBD versus placebo on (i) psychophysiological, craving and anxiety responses to alcohol and appetitive cues; (ii) tolerability measures including cognitive functioning.

Methods

Twenty-two non-treatment-seeking individuals with AUD (DSM-5) participated in a cross-over, double-blind, randomized trial, receiving either 800 mg of CBD or matched placebo over 3 days. A laboratory alcohol cue reactivity task with appetitive control (juice) and alcohol exposures, and subsequent recovery periods to examine regulation of cue-elicited responses after cue-offset (recovery) was completed, with psychophysiological indices of autonomic nervous system activity (skin conductance, high-frequency heart rate variability [HF-HRV]) and self-reported measures (alcohol craving and anxiety). Self-reported scales of sedation and neuropsychological executive function tasks were also completed.

Results

CBD sessions were significantly associated with elevated parasympathetic nervous system (PNS) activity across the task, as indicated by increased HF-HRV. Reductions in self-reported anxiety during cue exposure stages compared to placebo sessions were also evidenced. Reductions in self-reported alcohol craving after cue exposure were seen during CBD sessions only. There were no significant differences between CBD and placebo on executive functioning performance.

Conclusions

In a short-term regimen, CBD appears to modulate PNS activity, reduce cue-elicited anxiety during cue exposure and reduce alcohol craving after cue exposure while not significantly impairing cognition. Large, parallel clinical trials with longer term regimens are now needed to determine the therapeutic potential of CBD in the management of AUD.

Abstract Image

大麻二酚改变酒精提示反应任务中的心理生理、渴望和焦虑反应:一项交叉随机对照试验。
临床前研究表明,大麻二酚(CBD)可以减少寻求酒精的行为,并可能具有治疗酒精使用障碍(AUD)的潜力。在这项研究中,我们检验了CBD与安慰剂对以下方面的影响:(1)对酒精和食欲线索的心理生理、渴望和焦虑反应;(ii)包括认知功能在内的耐受性措施。方法:22名非寻求治疗的AUD患者(DSM-5)参加了一项交叉、双盲、随机试验,在3天内接受800毫克CBD或匹配的安慰剂。通过自主神经系统活动的心理生理指标(皮肤电导、高频心率变异性[HF-HRV])和自我报告的测量(酒精渴望和焦虑),完成了一项包括食欲控制(果汁)和酒精暴露的实验室酒精线索反应任务,以及随后的恢复期,以检查线索抵消(恢复)后线索引发反应的调节。自我报告的镇静量表和神经心理执行功能任务也完成了。结果:在整个任务过程中,CBD会话与副交感神经系统(PNS)活性升高显著相关,如增加的HF-HRV所示。与安慰剂组相比,提示暴露阶段自我报告的焦虑减少也得到了证明。在接触线索后,自我报告的酒精渴望减少只在CBD会议期间出现。CBD和安慰剂在执行功能表现上没有显著差异。结论:在短期方案中,CBD似乎可以调节PNS活动,减少线索暴露期间线索引发的焦虑,减少线索暴露后的酒精渴望,而不会显著损害认知。现在需要大型、平行的长期临床试验来确定CBD在AUD治疗中的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
5.40
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