GLP-1受体激动剂治疗酒精使用障碍

Gavin N Petrie,Leah M Mayo
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引用次数: 0

摘要

胰高血糖素样肽-1受体激动剂(GLP-1RAs),如semaglutide,广泛用于治疗代谢性疾病,包括2型糖尿病(T2D)和肥胖。这些药物主要通过促进胰岛素分泌起作用;然而,新出现的证据表明,其影响超出了代谢调节。在本期的JCI中,Farokhnia等人评估了GLP-1RAs与另一种T2D治疗方法二肽基肽酶-4抑制剂(DPP-4Is)对人类和临床前模型酒精消耗的影响。在人类中,GLP1-RAs,而不是DPP-4Is,与酒精消费量的减少有关。同样,DPP-4抑制对啮齿动物的酒精摄入量没有影响。这些发现促使我们进一步探索GLP-1RAs减少酒精消耗的机制,并重新定义我们治疗酒精使用障碍(AUD)的药物治疗方法,使其有可能成为早期减少危害的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GLP-1 receptor agonists for the treatment of alcohol use disorder.
Glucagon-like peptide-1 receptor agonists (GLP-1RAs), such as semaglutide, are widely used in the treatment of metabolic disorders, including type 2 diabetes (T2D) and obesity. These medications primarily function by enhancing insulin secretion; however, emerging evidence suggests that the effects extend beyond metabolic regulation. In this issue of the JCI, Farokhnia et al. evaluated the effects of GLP-1RAs alongside another T2D treatment, dipeptidyl peptidase-4 inhibitors (DPP-4Is), on alcohol consumption in humans and preclinical models. In humans, GLP1-RAs, but not DPP-4Is, were associated with reductions in alcohol consumption. Similarly, DPP-4 inhibition had no effect on alcohol intake in rodents. These findings invite further exploration of the mechanisms by which GLP-1RAs reduce alcohol consumption and redefine our pharmacotherapy approach to alcohol use disorder (AUD) by opening the possibility for application as an early harm-reduction tool.
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