Hassan Hazem E, Kelly Deanna, Honick Moshe, Shukla Sagar, Ibrahim Ahmed, Gorelick David A, Glassman Matthew, McMahon Robert P, Wehring Heidi J, Kearns Ann Marie, Feldman Stephanie, Yu Mingming, Bauer Ken, Wang Jia Bei
Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD, USA.
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Helwan University, Cairo, Egypt.
J Clin Pharmacol. 2017 Feb;57(2):151-160. doi: 10.1002/jcph.789. Epub 2016 Aug 4.
Cocaine use disorder (CUD) remains a significant public health challenge. l-Tetrahydropalmatine (l-THP), a well-tolerated and nonaddictive compound, shows promise for the management of CUD. Its pharmacologic profile includes blockade at dopamine and other monoamine receptors and attenuation of cocaine self-administration, reinstatement, and rewarding properties in rats. This study evaluated the safety of l-THP in human cocaine users and its influence on the safety and pharmacokinetics (PK) of cocaine. Twenty-four cocaine-using adult men were randomized to receive l-THP (30 mg twice a day orally) or placebo double-blind for 4 days, with an intranasal cocaine (40 mg) challenge on the fourth day. Safety and tolerability were evaluated using vital signs, ECG, clinical laboratory tests, and standardized self-report instruments. Peripheral venous blood was collected periodically and later assayed for l-THP and cocaine using highly sensitive and specific ultraperformance liquid chromatography-fluorescence detection (UPLC-FLD) methods. Twenty subjects completed the study, of whom 19 provided complete PK data. The short 3.5-day course of l-THP was safe and well tolerated and did not affect cocaine's PK or its acute cardiovascular effects. The cocaine AUC was 211.5 and 261.4 h·ng/mL, and the C was 83.3 and 104.5 ng/mL for the l-THP and placebo groups, respectively. In addition there were no significant differences in the number of side effects reported in each group (l-THP group 22 [48%], placebo group 24 [52%]) or vital signs including, heart rate, blood pressure, complete blood count, or ECG. These findings suggest that oral THP has promise for further development as a treatment for CUD.
可卡因使用障碍(CUD)仍然是一项重大的公共卫生挑战。左旋四氢巴马汀(l-THP)是一种耐受性良好且无成瘾性的化合物,在CUD的治疗方面显示出前景。其药理特性包括对多巴胺和其他单胺受体的阻断作用,以及在大鼠中减弱可卡因的自我给药、复吸和奖赏特性。本研究评估了l-THP在人类可卡因使用者中的安全性及其对可卡因安全性和药代动力学(PK)的影响。24名成年男性可卡因使用者被随机分为两组,双盲接受l-THP(每日口服两次,每次30mg)或安慰剂,为期4天,并在第4天接受鼻内给予可卡因(40mg)的激发试验。使用生命体征、心电图、临床实验室检查和标准化的自我报告工具评估安全性和耐受性。定期采集外周静脉血,随后使用高灵敏度和特异性的超高效液相色谱-荧光检测(UPLC-FLD)方法测定l-THP和可卡因。20名受试者完成了研究,其中19名提供了完整的PK数据。为期3.5天的l-THP短期疗程安全且耐受性良好,不影响可卡因的PK或其急性心血管效应。l-THP组和安慰剂组的可卡因曲线下面积(AUC)分别为211.5和261.4 h·ng/mL,峰浓度(Cmax)分别为83.3和104.5 ng/mL。此外,两组报告的副作用数量(l-THP组22例[48%],安慰剂组24例[52%])或包括心率、血压、全血细胞计数或心电图在内的生命体征均无显著差异。这些发现表明,口服THP有望进一步开发成为治疗CUD的药物。