Department of Psychiatry and Behavioral Sciences, Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, MD, 21224, USA.
Department of Psychiatry and Behavioral Sciences, Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, MD, 21224, USA.
Drug Alcohol Depend. 2018 Jun 1;187:254-260. doi: 10.1016/j.drugalcdep.2018.02.022. Epub 2018 Apr 17.
There is a clear need for advancing the treatment of cannabis use disorders. Prior research has demonstrated that dronabinol (oral THC) can dose-dependently suppress cannabis withdrawal and reduce the acute effects of smoked cannabis. The present study was conducted to evaluate whether high-dose dronabinol could reduce cannabis self-administration among daily users.
Non-treatment seeking daily cannabis users (N = 13) completed a residential within-subjects crossover study and were administered placebo, low-dose dronabinol (120 mg/day; 40 mg tid), or high-dose dronabinol (180-240 mg/day; 60-80 mg tid) for 12 consecutive days (order counterbalanced). During each 12-day dronabinol maintenance phase, participants were allowed to self-administer smoked cannabis containing <1% THC (placebo) or 5.7% THC (active) under forced-choice (drug vs. money) or progressive ratio conditions.
Participants self-administered significantly more active cannabis compared with placebo in all conditions. When active cannabis was available, self-administration was significantly reduced during periods of dronabinol maintenance compared with placebo maintenance. There was no difference in self-administration between the low- and high-dose dronabinol conditions.
Chronic dronabinol dosing can reduce cannabis self-administration in daily cannabis users and suppress withdrawal symptoms. Cannabinoid agonist medications should continue to be explored for therapeutic utility in the treatment of cannabis use disorders.
在推进大麻使用障碍的治疗方面存在明确的需求。先前的研究表明,屈大麻酚(口服 THC)可以剂量依赖性地抑制大麻戒断并减轻吸食大麻的急性效应。本研究旨在评估高剂量屈大麻酚是否可以减少每日使用者的大麻自我给药。
非治疗寻求的每日大麻使用者(N=13)完成了一项住院内个体交叉研究,并接受安慰剂、低剂量屈大麻酚(120mg/天;40mg tid)或高剂量屈大麻酚(180-240mg/天;60-80mg tid)连续 12 天(顺序平衡)。在每个 12 天的屈大麻酚维持阶段,参与者被允许在强制选择(药物与金钱)或递增比率条件下自行吸食含有<1%THC(安慰剂)或 5.7%THC(活性)的吸烟大麻。
与安慰剂相比,参与者在所有条件下均自行吸食更多的活性大麻。当有活性大麻时,与安慰剂维持期相比,屈大麻酚维持期的自我给药明显减少。低剂量和高剂量屈大麻酚条件之间的自我给药没有差异。
慢性屈大麻酚给药可减少每日大麻使用者的大麻自我给药,并抑制戒断症状。大麻素激动剂药物应继续探索其在治疗大麻使用障碍方面的治疗效用。