安非他明的表观遗传机制。

Journal of addiction & prevention Pub Date : 2015-01-01 Epub Date: 2015-02-09 DOI:10.13188/2330-2178.S100001
Talus J McCowan, Archana Dhasarathy, Lucia Carvelli
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引用次数: 5

摘要

安非他明(AMPH)是一种精神兴奋剂,也是治疗注意力缺陷多动障碍(ADHD)最常用的处方药。虽然用于治疗的剂量通常耐受性良好,但已知仍会出现许多副作用,如神经紧张、食欲不振和精神错乱。此外,AMPH很容易被寻求提高警觉性、减肥或运动表现的使用者滥用。越来越多的证据表明,滥用药物,包括AMPH,通过染色质修饰控制基因表达。然而,尽管有大量研究探讨了AMPH作用的分子机制,但只有少数研究探讨了AMPH引起的基因表达变化。本综述研究了慢性和急性AMPH治疗引起的表观遗传变化,并在相关的情况下包括其他精神兴奋剂如甲基苯丙胺和可卡因获得的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Epigenetic Mechanisms of Amphetamine.

The Epigenetic Mechanisms of Amphetamine.

Amphetamine (AMPH) is a psychostimulant and the most prescribed drug to treat attention deficit hyperactive disorder (ADHD). Although therapeutically used doses are generally well tolerated, numerous side effects are still known to occur, such as jitteriness, loss of appetite and psychosis. Moreover, AMPH is liable to be abused by users looking for increased alertness, weight loss or athletic performance. A growing body of evidence indicates that drugs of abuse, including AMPH, control gene expression through chromatin modifications. However, while numerous studies have investigated the molecular mechanisms of AMPH action, only a small number of studies have explored changes in gene expression caused by AMPH. This review examines the epigenetic changes induced by chronic and acute treatments with AMPH and includes, where relevant, data obtained with other psychostimulants such as methamphetamine and cocaine.

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