Virginia Tech Carilion School of Medicine, Roanoke, VA, USA.
J Psychopharmacol. 2012 Jul;26(7):973-81. doi: 10.1177/0269881111430745. Epub 2012 Jan 11.
Although cocaine dependence affects an estimated 1.6 million people in the USA, there are currently no medications approved for the treatment of this disorder. Experiments performed in animal models have demonstrated that inhibitors of the stress response effectively reduce intravenous cocaine self-administration. This exploratory, double-blind, placebo-controlled study was designed to assess the safety and efficacy of combinations of the cortisol synthesis inhibitor metyrapone, and the benzodiazepine oxazepam, in 45 cocaine-dependent individuals. The subjects were randomized to a total daily dose of 500 mg metyrapone/20 mg oxazepam (low dose), a total daily dose of 1500 mg metyrapone/20 mg oxazepam (high dose), or placebo for 6 weeks of treatment. The outcome measures were a reduction in cocaine craving and associated cocaine use as determined by quantitative measurements of the cocaine metabolite benzoylecgonine (BE) in urine at all visits. Of the randomized subjects, 49% completed the study. The combination of metyrapone and oxazepam was well tolerated and tended to reduce cocaine craving and cocaine use, with significant reductions at several time points when controlling for baseline scores. These data suggest that further assessments of the ability of the metyrapone and oxazepam combination to support cocaine abstinence in cocaine-dependent subjects are warranted.
尽管可卡因依赖症在美国估计影响了 160 万人,但目前尚无被批准用于治疗该疾病的药物。动物模型实验表明,应激反应抑制剂可有效减少静脉注射可卡因的自我给药。这项探索性、双盲、安慰剂对照研究旨在评估皮质醇合成抑制剂甲吡酮和苯二氮䓬类药物奥沙西泮联合用于 45 名可卡因依赖者的安全性和疗效。受试者被随机分配到 500mg 甲吡酮/20mg 奥沙西泮(低剂量)、1500mg 甲吡酮/20mg 奥沙西泮(高剂量)或安慰剂组,接受 6 周的治疗。疗效评估指标为通过尿液中可卡因代谢物苯甲酰爱康宁(BE)的定量测量,在所有就诊时减少可卡因渴望和相关可卡因使用。在随机受试者中,有 49%完成了研究。甲吡酮和奥沙西泮联合使用耐受良好,且倾向于减少可卡因渴望和可卡因使用,在控制基线评分的情况下,在几个时间点上有显著减少。这些数据表明,进一步评估甲吡酮和奥沙西泮联合用药对支持可卡因依赖者戒除可卡因的能力是合理的。