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对安非他明作用机制的新见解。

New insights into the mechanism of action of amphetamines.

作者信息

Fleckenstein Annette E, Volz Trent J, Riddle Evan L, Gibb James W, Hanson Glen R

机构信息

Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT 84112, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2007;47:681-98. doi: 10.1146/annurev.pharmtox.47.120505.105140.

Abstract

Amphetamine is a psychostimulant commonly used to treat several disorders, including attention deficit, narcolepsy, and obesity. Plasmalemmal and vesicular monoamine transporters, such as the neuronal dopamine transporter and the vesicular monoamine transporter-2, are two of its principal targets. This review focuses on new insights, obtained from both in vivo and in vitro studies, into the molecular mechanisms whereby amphetamine, and the closely related compounds methamphetamine and methylenedioxymethamphetamine, cause monoamine, and particularly dopamine, release. These mechanisms include amphetamine-induced exchange diffusion, reverse transport, and channel-like transport phenomena as well as the weak base properties of amphetamine. Additionally, amphetamine analogs may affect monoamine transporters through phosphorylation, transporter trafficking, and the production of reactive oxygen and nitrogen species. All of these mechanisms have potential implications for both amphetamine- and methamphetamine-induced neurotoxicity, as well as dopaminergic neurodegenerative diseases.

摘要

安非他命是一种精神兴奋剂,常用于治疗多种疾病,包括注意力缺陷、发作性睡病和肥胖症。质膜和囊泡单胺转运体,如神经元多巴胺转运体和囊泡单胺转运体-2,是其两个主要靶点。本综述重点关注从体内和体外研究中获得的关于安非他命以及密切相关化合物甲基苯丙胺和亚甲基二氧甲基苯丙胺导致单胺尤其是多巴胺释放的分子机制的新见解。这些机制包括安非他命诱导的交换扩散、逆向转运和通道样转运现象以及安非他命的弱碱性质。此外,安非他命类似物可能通过磷酸化、转运体运输以及活性氧和氮物种的产生来影响单胺转运体。所有这些机制对安非他命和甲基苯丙胺诱导的神经毒性以及多巴胺能神经退行性疾病都具有潜在影响。

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