GDF15型
机制(生物学)
兴奋剂
受体
内分泌学
细胞生物学
生物
神经科学
计算生物学
生物化学
哲学
认识论
作者
Olivier Bénichou,Tamer Coşkun,Malgorzata D. Gonciarz,Parag Garhyan,Andrew C. Adams,Yu Du,James D. Dunbar,Jennifer A. Martin,Kieren J. Mather,Richard T. Pickard,Vincent L. Reynolds,Deborah Robins,Simbarashe P. Zvada,Paul J. Emmerson
出处
期刊:Cell Metabolism
[Cell Press]
日期:2023-01-10
卷期号:35 (2): 274-286.e10
被引量:62
标识
DOI:10.1016/j.cmet.2022.12.011
摘要
GDF15 and its receptor GFRAL/RET form a non-homeostatic system that regulates food intake and body weight in preclinical species. Here, we describe a GDF15 analog, LY3463251, a potent agonist at the GFRAL/RET receptor with prolonged pharmacokinetics. In rodents and obese non-human primates, LY3463251 decreased food intake and body weight with no signs of malaise or emesis. In a first-in-human study in healthy participants, single subcutaneous LY3463251 injections showed a safety and pharmacokinetic profile supporting further clinical development with dose-dependent nausea and emesis in a subset of individuals. A subsequent 12-week multiple ascending dose study in overweight and obese participants showed that LY3463251 induced significant decreases in food intake and appetite scores associated with modest body weight reduction independent of nausea and emesis (clinicaltrials.gov: NCT03764774). These observations demonstrate that agonism of the GFRAL/RET system can modulate energy balance in humans, though the decrease in body weight is surprisingly modest, suggesting challenges in leveraging the GDF15 system for clinical weight-loss applications.
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