Borner Tito, Pataro Allison M, Doebley Sarah A, Furst Charles D, White Alex D, Gao Serena X, Chow Angela, Sanchez-Navarro Marcos J, Ghidewon Misgana Y, Halas Julia G, Mohiby Allaha Z, Willard Francis S, Grill Harvey J, Ai Minrong, Samms Ricardo J, Hayes Matthew R, De Jonghe Bart C
Department of Biobehavioral Health Sciences, University of Pennsylvania, School of Nursing, Philadelphia, PA, USA.
Department of Psychiatry, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.
Sci Adv. 2025 Jun 20;11(25):eadu1589. doi: 10.1126/sciadv.adu1589. Epub 2025 Jun 18.
Glucagon-like peptide-1 receptor (GLP-1R)/glucose-dependent insulinotropic peptide receptor (GIPR) agonistic analogs have yielded superior results in enhancing glycemic control and weight management compared to GLP-1R agonism alone. Intriguingly, GIPR agonism appears to induce antiemetic effects, potentially alleviating part of the nausea and vomiting side effects common to GLP-1R agonists like semaglutide. Here, we show in rats and shrews that GIPR agonism blocks emesis and attenuates other malaise behaviors elicited by GLP-1R activation while maintaining reduced food intake and body weight loss and improved glucose tolerance. The GLP-1R/GIPR agonist tirzepatide induced significantly fewer side effects than equipotent doses of semaglutide. These findings underscore the therapeutic potential of combined pharmaceutical strategies activating both incretin systems, leading to enhanced therapeutic index and reduced occurrence of nausea and vomiting for obesity and diabetes treatments.
与单独使用胰高血糖素样肽-1受体(GLP-1R)激动剂相比,胰高血糖素样肽-1受体(GLP-1R)/葡萄糖依赖性促胰岛素多肽受体(GIPR)激动类似物在改善血糖控制和体重管理方面产生了更优的效果。有趣的是,GIPR激动似乎会产生止吐作用,可能减轻司美格鲁肽等GLP-1R激动剂常见的部分恶心和呕吐副作用。在此,我们在大鼠和鼩鼱身上表明,GIPR激动可阻断呕吐,并减轻GLP-1R激活引发的其他不适行为,同时保持食物摄入量减少、体重减轻以及葡萄糖耐量改善。与等效剂量的司美格鲁肽相比,GLP-1R/GIPR激动剂替尔泊肽引起的副作用明显更少。这些发现强调了激活两种肠促胰岛素系统的联合药物策略的治疗潜力,可提高治疗指数,并减少肥胖症和糖尿病治疗中恶心和呕吐的发生。