胰高血糖素受体
减肥
血糖性
兴奋剂
内分泌学
内科学
胰高血糖素样肽-1
医学
胰高血糖素样肽1受体
耐受性
胰高血糖素
受体
糖尿病
2型糖尿病
肥胖
胰岛素
不利影响
作者
Tamer Coşkun,Shweta Urva,William C. Roell,Hongchang Qu,Corina Loghin,Julie S. Moyers,Libbey S. O’Farrell,Daniel A. Briere,Kyle W. Sloop,Melissa K. Thomas,Valentina Pirro,David B. Wainscott,Francis S. Willard,Matthew Abernathy,LaRonda L. Morford,Yu Du,Charles T. Benson,Ruth E. Gimeno,Axel Haupt,Zvonko Miličević
出处
期刊:Cell Metabolism
[Cell Press]
日期:2022-08-18
卷期号:34 (9): 1234-1247.e9
被引量:154
标识
DOI:10.1016/j.cmet.2022.07.013
摘要
With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
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