De La Garza Richard, Bubar Marcy J, Carbone Crystal L, Moeller F Gerard, Newton Thomas F, Anastasio Noelle C, Harper Tod A, Ware David L, Fuller Michael A, Holstein Gaylyn J, Jayroe Jason B, Bandak Stephen I, Reiman Kirsten Z, Neale Ann C, Pickford Lesley B, Cunningham Kathryn A
Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX, United States.
Center for Addiction Research, University of Texas Medical Branch, Galveston, TX, United States.
Prog Neuropsychopharmacol Biol Psychiatry. 2015 Jun 3;59:40-48. doi: 10.1016/j.pnpbp.2015.01.009. Epub 2015 Jan 17.
In the present study, we tested the hypothesis that the potent and selective dopamine-β-hydroxylase (DβH) inhibitor nepicastat would have minimal effects on cardiovascular and pharmacokinetic parameters associated with cocaine administration and would reduce the positive subjective effects produced by cocaine. We conducted a double-blind, placebo-controlled, inpatient study of oral nepicastat (0, 80 and 160mg) concurrent with intravenous (IV) cocaine (0, 10, 20 and 40mg) in non-treatment seeking participants who metcriteria for cocaine use disorder. Safety analyses revealed that nepicastat was well-tolerated and there were no differences in adverse events observed after nepicastat plus cocaine vs. cocaine alone. In addition, the pharmacokinetic properties of cocaine administration were not altered by nepicastat treatment. Cocaine-induced cardiovascular and subjective effects were evaluated for completers in the cohort randomized to nepicastat (n=13) using a within-subjects statistical analysis strategy. Specifically, the cardiovascular and subjective effects of cocaine were assessed in the presence of placebo (0mg), 80mg of nepicastat or 160mg of nepicastat on study Days 4, 8 and 12, respectively. Analyses revealed a main effect of nepicastat to reduce several cocaine-induced positive subjective effects. Taken together, these data indicate that nepicastat is safe when co-administered with cocaine and may suppress its positive subjective effects, and may be viable as a pharmacotherapy for treatment of cocaine use disorder.
在本研究中,我们检验了以下假设:强效且具有选择性的多巴胺-β-羟化酶(DβH)抑制剂奈必司他对与可卡因给药相关的心血管和药代动力学参数影响极小,并能减轻可卡因产生的积极主观效应。我们对符合可卡因使用障碍标准的非寻求治疗参与者进行了一项双盲、安慰剂对照的住院研究,口服奈必司他(0、80和160毫克)并同时静脉注射(IV)可卡因(0、10、20和40毫克)。安全性分析显示,奈必司他耐受性良好,奈必司他加可卡因组与单独使用可卡因组观察到的不良事件无差异。此外,奈必司他治疗未改变可卡因给药的药代动力学特性。使用受试者内统计分析策略,对随机分配至奈必司他组(n = 13)的队列中的完成者评估可卡因诱导的心血管和主观效应。具体而言,在研究的第4、8和12天,分别在安慰剂(0毫克)、80毫克奈必司他或160毫克奈必司他存在的情况下评估可卡因的心血管和主观效应。分析显示,奈必司他具有减轻几种可卡因诱导的积极主观效应的主要作用。综上所述,这些数据表明,奈必司他与可卡因联合使用时是安全的,可能会抑制其积极主观效应,并且可能作为治疗可卡因使用障碍的药物疗法是可行的。