FGF21型
热卡限制
脂肪组织
生物
激素
内分泌学
内科学
减肥
代谢综合征
肥胖
医学
成纤维细胞生长因子
受体
作者
Cristal M. Hill,Diana C. Albarado,Lucia G. Coco,Redin A. Spann,Md Shahjalal Hossain Khan,Emily Qualls‐Creekmore,David H. Burk,Susan J. Burke,J. Jason Collier,Sangho Yu,David H. McDougal,Hans‐Rudolf Berthoud,Heike Münzberg,Andrzej Bartke,Christopher D. Morrison
标识
DOI:10.1038/s41467-022-29499-8
摘要
Dietary protein restriction is increasingly recognized as a unique approach to improve metabolic health, and there is increasing interest in the mechanisms underlying this beneficial effect. Recent work indicates that the hormone FGF21 mediates the metabolic effects of protein restriction in young mice. Here we demonstrate that protein restriction increases lifespan, reduces frailty, lowers body weight and adiposity, improves physical performance, improves glucose tolerance, and alters various metabolic markers within the serum, liver, and adipose tissue of wildtype male mice. Conversely, mice lacking FGF21 fail to exhibit metabolic responses to protein restriction in early life, and in later life exhibit early onset of age-related weight loss, reduced physical performance, increased frailty, and reduced lifespan. These data demonstrate that protein restriction in aging male mice exerts marked beneficial effects on lifespan and metabolic health and that a single metabolic hormone, FGF21, is essential for the anti-aging effect of this dietary intervention.
科研通智能强力驱动
Strongly Powered by AbleSci AI