Mesenchymal stem cells as a promising therapy for alcohol use disorder.

International review of neurobiology Pub Date : 2024-01-01 Epub Date: 2024-07-25 DOI:10.1016/bs.irn.2024.07.002
Javiera Gallardo, Pablo Berríos-Cárcamo, Fernando Ezquer
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Abstract

Alcohol Use Disorder (AUD) is a highly prevalent medical condition characterized by impaired control over alcohol consumption, despite negative consequences on the individual's daily life and health. There is increasing evidence suggesting that chronic alcohol intake, like other addictive drugs, induces neuroinflammation and oxidative stress, disrupting glutamate homeostasis in the main brain areas related to drug addiction. This review explores the potential application of mesenchymal stem cells (MSCs)-based therapy for the treatment of AUD. MSCs secrete a broad array of anti-inflammatory and antioxidant molecules, thus, the administration of MSCs, or their secretome, could reduce neuroinflammation and oxidative stress in the brain. These effects correlate with an increase in the expression of the main glutamate transporter, GLT1, which, through the normalization of the extracellular glutamate levels, could mediate the inhibitory effect of MSCs' secretome on chronic alcohol consumption, thus highlighting GLT1 as a central target to reduce chronic alcohol consumption.

间充质干细胞是一种治疗酒精使用障碍的有效方法。
酒精使用障碍(AUD)是一种发病率很高的疾病,其特点是对酒精消费的控制能力减弱,尽管会对个人的日常生活和健康造成负面影响。越来越多的证据表明,长期摄入酒精和其他成瘾药物一样,会诱发神经炎症和氧化应激,破坏与药物成瘾有关的主要脑区的谷氨酸平衡。这篇综述探讨了基于间充质干细胞(MSCs)疗法治疗AUD的潜在应用。间充质干细胞可分泌多种抗炎和抗氧化分子,因此,服用间充质干细胞或其分泌物可减轻大脑神经炎症和氧化应激。这些作用与主要谷氨酸转运体 GLT1 表达的增加有关,GLT1 通过使细胞外谷氨酸水平正常化,可介导间叶干细胞分泌物对慢性酒精消耗的抑制作用,从而突出了 GLT1 作为减少慢性酒精消耗的核心靶点的作用。
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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