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利用N-乙酰半胱氨酸靶向氧化还原调节来治疗物质使用障碍。

Targeting redox regulation to treat substance use disorder using N‐acetylcysteine.

作者信息

Womersley Jacqueline S, Townsend Danyelle M, Kalivas Peter W, Uys Joachim D

机构信息

Department of Cellular and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, 409 Drug Discovery Building, 70 President Street, Charleston, SC, 29425, USA.

Department of Drug Discover and Biomedical Sciences, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Eur J Neurosci. 2019 Aug;50(3):2538-2551. doi: 10.1111/ejn.14130. Epub 2018 Sep 24.

Abstract

Substance use disorder (SUD) is a chronic relapsing disorder characterized by transitioning from acute drug reward to compulsive drug use. Despite the heavy personal and societal burden of SUDs, current treatments are limited and unsatisfactory. For this reason, a deeper understanding of the mechanisms underlying addiction is required. Altered redox status, primarily due to drug-induced increases in dopamine metabolism, is a unifying feature of abused substances. In recent years, knowledge of the effects of oxidative stress in the nervous system has evolved from strictly neurotoxic to include a more nuanced role in redox-sensitive signaling. More specifically, S-glutathionylation, a redox-sensitive post-translational modification, has been suggested to influence the response to drugs of abuse. In this review we will examine the evidence for redox-mediating drugs as therapeutic tools focusing on N-acetylcysteine as a treatment for cocaine addiction. We will conclude by suggesting future research directions that may further advance this field.

摘要

物质使用障碍(SUD)是一种慢性复发性疾病,其特征是从急性药物奖赏转变为强迫性药物使用。尽管SUD给个人和社会带来了沉重负担,但目前的治疗方法有限且不尽人意。因此,需要更深入地了解成瘾的潜在机制。氧化还原状态的改变主要是由于药物引起的多巴胺代谢增加,这是滥用物质的一个共同特征。近年来,关于氧化应激在神经系统中的作用的认识已从严格的神经毒性发展到包括在氧化还原敏感信号传导中更细微的作用。更具体地说,S-谷胱甘肽化是一种氧化还原敏感的翻译后修饰,已被认为会影响对滥用药物的反应。在这篇综述中,我们将研究氧化还原介导药物作为治疗工具的证据,重点关注N-乙酰半胱氨酸作为可卡因成瘾的治疗方法。我们将通过提出可能进一步推动该领域发展的未来研究方向来得出结论。

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