Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Drug Alcohol Depend. 2013 Feb 1;128(1-2):64-70. doi: 10.1016/j.drugalcdep.2012.08.001. Epub 2012 Aug 22.
Prior studies have separately examined the effects of dronabinol (oral THC) on cannabis withdrawal, cognitive performance, and the acute effects of smoked cannabis. A single study examining these clinically relevant domains would benefit the continued evaluation of dronabinol as a potential medication for the treatment of cannabis use disorders.
Thirteen daily cannabis smokers completed a within-subject crossover study and received 0, 30, 60 and 120mg dronabinol per day for 5 consecutive days. Vital signs and subjective ratings of cannabis withdrawal, craving and sleep were obtained daily; outcomes under active dose conditions were compared to those obtained under placebo dosing. On the 5th day of medication maintenance, participants completed a comprehensive cognitive performance battery and then smoked five puffs of cannabis for subjective effects evaluation. Each dronabinol maintenance period occurred in a counterbalanced order and was separated by 9 days of ad libitum cannabis use.
Dronabinol dose-dependently attenuated cannabis withdrawal and resulted in few adverse side effects or decrements in cognitive performance. Surprisingly, dronabinol did not alter the subjective effects of smoked cannabis, but cannabis-induced increases in heart rate were attenuated by the 60 and 120mg doses.
Dronabinol's ability to dose-dependently suppress cannabis withdrawal may be therapeutically beneficial to individuals trying to stop cannabis use. The absence of gross cognitive impairment or side effects in this study supports safety of doses up to 120mg/day. Continued evaluation of dronabinol in targeted clinical studies of cannabis treatment, using an expanded range of doses, is warranted.
先前的研究分别考察了大麻戒断、认知表现和吸食大麻的急性效应方面,大麻花(口服四氢大麻酚)的影响。单一研究检查这些临床相关领域将有利于继续评估大麻隆作为治疗大麻使用障碍的潜在药物。
13 名每日吸食大麻的吸烟者完成了一项在体交叉研究,并在连续 5 天内每天接受 0、30、60 和 120mg 大麻隆治疗。每日获取生命体征和大麻戒断、渴望和睡眠的主观评分;在活性剂量条件下的结果与安慰剂给药下获得的结果进行比较。在药物维持的第 5 天,参与者完成了一项全面的认知表现测试,然后吸食了五口大麻,以评估主观效应。每个大麻隆维持期以平衡的顺序发生,并与 9 天的自由吸食大麻期隔开。
大麻隆剂量依赖性地减轻了大麻戒断,并导致很少出现不良反应或认知表现下降。令人惊讶的是,大麻隆并没有改变吸食大麻的主观效应,但大麻引起的心率增加被 60 和 120mg 剂量所减弱。
大麻隆能够剂量依赖性地抑制大麻戒断,这对试图停止大麻使用的个体可能具有治疗益处。在这项研究中,没有出现严重的认知障碍或副作用,支持高达 120mg/天的剂量安全。在针对大麻治疗的目标临床研究中,继续评估大麻隆,使用更广泛的剂量,是有必要的。