纳曲酮-安非他酮联合用药不会影响人类可卡因自我给药

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Sean D. Regnier , William W. Stoops , Joshua A. Lile , Joseph L. Alcorn III , B. Levi Bolin , Anna R. Reynolds , Lon R. Hays , Abner O. Rayapati , Craig R. Rush
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引用次数: 0

摘要

尽管进行了近四十年的研究,但美国食品药品监督管理局尚未批准可卡因使用障碍的药物治疗。本研究确定了纳曲酮-安非他酮联合用药作为可卡因使用障碍的假定药物治疗的初步疗效、安全性和耐受性。三十一(31)名可卡因使用障碍的非寻求治疗的参与者完成了一项混合设计的人体实验室研究。参与者被随机分配到纳曲酮条件下(即,0,50 mg/天;受试者之间因素),并在进行实验前至少四天维持递增剂量的安非他酮(即,100,200,400 mg/天,受试者内部因素)。然后使用改良的渐进比率和复发程序确定可卡因自行给药(IN,0,40,80mg)。还测量了主观和心血管影响。在安慰剂维持期间,可卡因在自我给药、主观结果(如“像药”)和心血管指标(如心率、血压)方面产生了典型的剂量相关增加。纳曲酮和安非他酮单独使用或联合使用均未显著减少两种方法的自我给药。低剂量的安非他酮(即100 mg)减弱了可卡因对“类药物”和“刺激”主观指标的影响。单独使用纳曲酮和安非他酮以及与可卡因联合使用均未观察到意外的不良反应。总之,这些结果不支持使用这些安非他酮-纳曲酮组合治疗可卡因使用障碍。未来的研究应该确定新的药物组合是否可以减少可卡因的自我给药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Naltrexone-bupropion combinations do not affect cocaine self-administration in humans

The FDA has not yet approved a pharmacotherapy for cocaine use disorder despite nearly four decades of research. This study determined the initial efficacy, safety, and tolerability of naltrexone-bupropion combinations as a putative pharmacotherapy for cocaine use disorder.

Thirty-one (31) non-treatment seeking participants with cocaine use disorder completed a mixed-design human laboratory study. Participants were randomly assigned to the naltrexone conditions (i.e., 0, 50 mg/day; between-subject factor) and maintained on escalating doses of bupropion (i.e., 0, 100, 200, 400 mg/day; within-subject factor) for at least four days prior to the conduct of experimental sessions. Cocaine self-administration (IN, 0, 40, 80 mg) was then determined using a modified progressive ratio and relapse procedure. Subjective and cardiovascular effects were also measured. Cocaine produced prototypical dose-related increases in self-administration, subjective outcomes (e.g., “Like Drug”), and cardiovascular indices (e.g., heart rate, blood pressure) during placebo maintenance. Naltrexone and bupropion alone, or in combination, did not significantly decrease self-administration on either procedure. Low doses of bupropion (i.e., 100 mg) blunted the effects of the cocaine on subjective measures of “Like Drug” and “Stimulated”. No unexpected adverse effects were observed with naltrexone and bupropion, alone and combined, in conjunction with cocaine.

Together, these results do not support the use of these bupropion-naltrexone combinations for the treatment of cocaine use disorder. Future research should determine if novel drug combinations may decrease cocaine self-administration.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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