Therapeutic Targeting of the GIP Receptor-Revisiting the Controversies.

Diabetes Pub Date : 2025-06-16 DOI:10.2337/db25-0393
Jonathan E Campbell, Daniel J Drucker
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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.

GIP受体的靶向治疗——重新审视争议。
目前和新兴的治疗目标体重管理策略包括胰高血糖素样肽1受体(GLP-1R)的激动作用与葡萄糖依赖性胰岛素性多肽受体(GIPR)的激动作用或拮抗作用配对。表面上看,这两种方法似乎是矛盾的,但在临床研究中,它们对减肥产生了相似的效果。支持这两种方法基本原理的论点在这些基于临床前研究、人类遗传学和临床结果的点对点文章中提出。在这里,我们试图通过评估从现有证据中得出的主要假设来调和两种相反的方法如何对体重产生相似的影响。
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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