生物
激活剂(遗传学)
骨骼肌
炎症
肌肉萎缩
萎缩
骨矿物
内分泌学
肌萎缩
骨量
内科学
基因
生物化学
骨质疏松症
免疫学
遗传学
医学
作者
Evi M. Mercken,Sarah J. Mitchell,Alejandro Martín‐Montalvo,Robin K. Minor,Maria Almeida,Ana P. Gomes,Morten Scheibye‐Knudsen,Hector H. Palacios,Jordan J. Licata,Yongqing Zhang,Kevin G. Becker,Husam Khraiwesh,José A. González‐Reyes,José M. Villalba,Joseph A. Baur,Peter J. Elliott,Christoph Westphal,George P. Vlasuk,James L. Ellis,David Sinclair
出处
期刊:Aging Cell
[Wiley]
日期:2014-06-16
卷期号:13 (5): 787-796
被引量:224
摘要
Increased expression of SIRT1 extends the lifespan of lower organisms and delays the onset of age-related diseases in mammals. Here, we show that SRT2104, a synthetic small molecule activator of SIRT1, extends both mean and maximal lifespan of mice fed a standard diet. This is accompanied by improvements in health, including enhanced motor coordination, performance, bone mineral density, and insulin sensitivity associated with higher mitochondrial content and decreased inflammation. Short-term SRT2104 treatment preserves bone and muscle mass in an experimental model of atrophy. These results demonstrate it is possible to design a small molecule that can slow aging and delay multiple age-related diseases in mammals, supporting the therapeutic potential of SIRT1 activators in humans.
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