Neuroglia in substance use disorders.

Q2 Medicine
Emily M Castro, Shahrdad Lotfipour, Frances M Leslie
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引用次数: 0

Abstract

Substance use disorders (SUD) remain a major public health concern in which individuals are unable to control their use of substances despite significant harm and negative consequences. Drugs of abuse dysregulate major brain and behavioral functions. Glial cells, primarily microglia and astrocytes, play a crucial role in these drug-induced molecular and behavioral changes. This review explores preclinical and clinical studies of how neuroglia and their associated neuroinflammatory responses contribute to SUD and reward-related properties. We evaluate preclinical and clinical evidence for targeting neuroglia as therapeutic interventions. In addition, we evaluate the literature on the gut microbiome and its role in SUD. Clinical treatments are most effective for reducing drug cravings, and some have yielded promising results in other measures of drug use. N-Acetylcysteine, through modulation of cysteine-glutamate antiporter of glial cells, shows encouraging results across a variety of drug classes. Neuroglia and gut microbiome interactions are important factors to consider with regard to SUD and could lead to novel therapeutic avenues. Age- and sex-dependent properties of neuroglia, gut microbiome, and drug use behaviors are important areas in need of further investigation.

物质使用障碍中的神经胶质细胞。
物质使用障碍(SUD)仍然是一个主要的公共卫生问题,其中个人无法控制他们对物质的使用,尽管有重大伤害和负面后果。滥用药物使主要的大脑和行为功能失调。胶质细胞,主要是小胶质细胞和星形胶质细胞,在这些药物诱导的分子和行为改变中起着至关重要的作用。本文综述了神经胶质细胞及其相关的神经炎症反应如何促进SUD和奖励相关特性的临床前和临床研究。我们评估针对神经胶质细胞作为治疗干预的临床前和临床证据。此外,我们评估了关于肠道微生物群及其在SUD中的作用的文献。临床治疗对于减少对药物的渴望是最有效的,有些治疗在其他药物使用方面也取得了令人鼓舞的结果。n -乙酰半胱氨酸通过调节神经胶质细胞的半胱氨酸-谷氨酸反转运蛋白,在各种药物类别中显示出令人鼓舞的结果。神经胶质细胞和肠道微生物组的相互作用是考虑SUD的重要因素,并可能导致新的治疗途径。神经胶质细胞、肠道微生物组和药物使用行为的年龄和性别依赖特性是需要进一步研究的重要领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Handbook of clinical neurology
Handbook of clinical neurology Medicine-Neurology (clinical)
CiteScore
4.10
自引率
0.00%
发文量
302
期刊介绍: The Handbook of Clinical Neurology (HCN) was originally conceived and edited by Pierre Vinken and George Bruyn as a prestigious, multivolume reference work that would cover all the disorders encountered by clinicians and researchers engaged in neurology and allied fields. The first series of the Handbook (Volumes 1-44) was published between 1968 and 1982 and was followed by a second series (Volumes 45-78), guided by the same editors, which concluded in 2002. By that time, the Handbook had come to represent one of the largest scientific works ever published. In 2002, Professors Michael J. Aminoff, François Boller, and Dick F. Swaab took on the responsibility of supervising the third (current) series, the first volumes of which published in 2003. They have designed this series to encompass both clinical neurology and also the basic and clinical neurosciences that are its underpinning. Given the enormity and complexity of the accumulating literature, it is almost impossible to keep abreast of developments in the field, thus providing the raison d''être for the series. The series will thus appeal to clinicians and investigators alike, providing to each an added dimension. Now, more than 140 volumes after it began, the Handbook of Clinical Neurology series has an unparalleled reputation for providing the latest information on fundamental research on the operation of the nervous system in health and disease, comprehensive clinical information on neurological and related disorders, and up-to-date treatment protocols.
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