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GIP受体的治疗靶向——重新审视争议

Therapeutic Targeting of the GIP Receptor-Revisiting the Controversies.

作者信息

Campbell Jonathan E, Drucker Daniel J

机构信息

Duke Molecular Physiology Institute, Durham, NC.

Lunenfeld-Tanenbaum Research Institute, Sinai Health System, University of Toronto, Toronto, Ontario, Canada.

出版信息

Diabetes. 2025 Aug 1;74(8):1320-1325. doi: 10.2337/db25-0393.

Abstract

Current and emerging strategies to therapeutically target weight management include pairing agonism of the glucagon-like peptide 1 receptor (GLP-1R) with either agonism or antagonism of the glucose-dependent insulinotropic polypeptide receptor (GIPR). On the surface, these two approaches seem contradictory, yet they have produced similar effects for weight loss in clinical studies. Arguments that support the rationale for both approaches are made in these point-counterpoint articles, founded on preclinical studies, human genetics, and clinical outcomes. Here, we attempt to reconcile how two opposing approaches can produce similar effects on body weight by evaluating the leading hypotheses derived from the available evidence.

摘要

目前以及新出现的针对体重管理的治疗策略包括将胰高血糖素样肽1受体(GLP-1R)激动与葡萄糖依赖性促胰岛素多肽受体(GIPR)激动或拮抗相结合。从表面上看,这两种方法似乎相互矛盾,但在临床研究中它们对体重减轻产生了相似的效果。在这些基于临床前研究、人类遗传学和临床结果的针锋相对的文章中,提出了支持这两种方法基本原理的论据。在这里,我们试图通过评估从现有证据得出的主要假设,来调和两种相反的方法如何能对体重产生相似的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e01c/12278791/05b7c1c769e8/db250393f1.jpg

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