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“摇头丸”类兴奋剂成瘾机制及三种新型苯丙胺类兴奋剂的强化效应。

"Ecstasy" to addiction: Mechanisms and reinforcing effects of three synthetic cathinone analogs of MDMA.

机构信息

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX, USA.

出版信息

Neuropharmacology. 2018 May 1;133:171-180. doi: 10.1016/j.neuropharm.2018.01.020. Epub 2018 Jan 31.

Abstract

This study aimed to address the mechanisms and reinforcing effects of three synthetic cathinone analogs of MDMA commonly reported in "Ecstasy" formulations: methylone, butylone, and pentylone. Whole-cell patch clamp techniques were used to assess the mechanism of each compound at the dopamine and serotonin transporters. Separate groups of rats were trained to discriminate methamphetamine, DOM, or MDMA from vehicle. Substitution studies were performed in each group and antagonism studies with SCH23390 were performed against each compound that produced substitution. Self-administration of each compound was evaluated under a progressive ratio schedule of reinforcement. Each compound produced an inward current at the serotonin transporter, but little or no current at the dopamine transporter. Each of the test compounds substituted fully for the discriminative stimulus effects of methamphetamine, methylone and butylone substituted partially for DOM and fully for MDMA, whereas pentylone failed to substitute for DOM and substituted only partially for MDMA. SCH23390 fully and dose-dependently attenuated methamphetamine-appropriate responding produced by each test compound, but was least potent against pentylone. MDMA-appropriate responding was minimally affected by SCH23390. Each test compound was robustly self-administered with pentylone producing the greatest self-administration at the doses tested. Given the prevalence of synthetic cathinones in "Ecstasy" formulations, these data indicate that adulterated "Ecstasy" formulations may drive more compulsive drug use than those containing only MDMA.

摘要

这项研究旨在探讨三种常见于“摇头丸”制剂中的合成卡西酮类似物(即甲卡西酮、丁基酮和戊基酮)对 MDMA 的作用机制和强化效应。采用全细胞膜片钳技术评估了每种化合物在多巴胺和血清素转运体上的作用机制。将不同组的大鼠训练为区分安非他命、DOM 或 MDMA 与载体。在每组中进行了替代研究,并针对产生替代作用的每种化合物进行了与 SCH23390 的拮抗研究。在递增比例强化方案下评估了每种化合物的自我给药情况。每种化合物在血清素转运体上产生内向电流,但在多巴胺转运体上产生的电流很少或没有。测试的化合物均完全替代了安非他命的辨别刺激效应,甲卡西酮和丁基酮部分替代了 DOM,完全替代了 MDMA,而戊基酮未能替代 DOM,仅部分替代了 MDMA。SCH23390 完全且剂量依赖性地减弱了每种测试化合物引起的安非他命样反应,但对戊基酮的作用最弱。SCH23390 对 MDMA 样反应的影响最小。每种测试化合物都被强烈地自我给药,戊基酮在测试剂量下产生的自我给药最多。鉴于合成卡西酮在“摇头丸”制剂中的普遍存在,这些数据表明,与仅含有 MDMA 的“摇头丸”制剂相比,掺假的“摇头丸”制剂可能会导致更强迫性的药物使用。

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