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脱氢表雄酮(DHEA)在觅药行为中的作用。

The role of dehydroepiandrosterone (DHEA) in drug-seeking behavior.

机构信息

The Mina & Everard Goodman Faculty of Life Sciences, The Leslie Susan Gonda Goldschmied Multidisciplinary Brain Research Center, Bar-Ilan University, Ramat Gan, Israel.

出版信息

Neurosci Biobehav Rev. 2010 Nov;35(2):303-14. doi: 10.1016/j.neubiorev.2010.03.003. Epub 2010 Mar 12.

Abstract

Conventional substance-abuse treatments have only had limited success especially for drugs such as cocaine, methamphetamine and nicotine. Newer data have begun to shed light on the complexity of the addictive process and new treatment approaches, including interference with brain neurosteroids, to attenuate drug-seeking behavior, are in advanced stages of development. Neurosteroids are synthesized in the brain and peripheral tissues, from cholesterol or steroidal precursors imported from peripheral sources. The most abundant neurosteroids in the human body are DHEA and its sulfate ester, DHEAS. These neurosteroids can act as modulators of neurotransmitter receptors, such as γ-aminobutyric-acid-type A (GABA(A)), NMDA, and sigma-1 receptors which may contribute to apparent enduring behavioral manifestations facilitated by substances of abuse. Neurosteroid concentrations respond to environmental and behavioral circumstances, such as stress and mood, both which are involved in the progression of substance use that advance substance addiction. This article reviews the current literature pertaining to neurosteroids and substances of abuse, focusing on DHEA, and discusses its role in drug-seeking behavior as suggested by preclinical observations.

摘要

传统的物质滥用治疗方法仅取得了有限的成功,特别是对于可卡因、冰毒和尼古丁等药物。新的研究数据开始揭示成瘾过程的复杂性,包括干扰脑神经甾体,以减轻觅药行为,这些新的治疗方法正处于开发的高级阶段。神经甾体在大脑和外周组织中从胆固醇或从外周来源输入的类固醇前体合成。人体内最丰富的神经甾体是 DHEA 和其硫酸盐酯 DHEAS。这些神经甾体可以作为神经递质受体的调节剂,如γ-氨基丁酸 A 型(GABA(A))、NMDA 和 sigma-1 受体,这可能有助于解释滥用物质促进的明显持久的行为表现。神经甾体的浓度会对外界环境和行为情况做出反应,如压力和情绪,这些因素都参与了物质使用的进展,从而导致物质成瘾。本文回顾了与神经甾体和滥用物质相关的当前文献,重点介绍了 DHEA,并根据临床前观察讨论了其在觅药行为中的作用。

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