安普克
激活剂(遗传学)
心肌肥大
内分泌学
内科学
蛋白激酶A
葡萄糖稳态
肌肉肥大
化学
平衡
胰岛素抵抗
医学
胰岛素
生物化学
受体
酶
作者
Robert W. Myers,Hong-Ping Guan,Juliann Ehrhart,Aleksandr Petrov,S. Prahalada,Effie Tozzo,Xiao-Dong Yang,Marc M. Kurtz,Maria E. Trujillo,Dinko González Trotter,Danqing Feng,Shiyao Xu,George J. Eiermann,Marie A. Holahan,Daniel Rubins,Stacey Conarello,Xiaoda Niu,Sandra C. Souza,Corin O. Miller,Jinqi Liu
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2017-07-14
卷期号:357 (6350): 507-511
被引量:278
标识
DOI:10.1126/science.aah5582
摘要
5'-Adenosine monophosphate-activated protein kinase (AMPK) is a master regulator of energy homeostasis in eukaryotes. Despite three decades of investigation, the biological roles of AMPK and its potential as a drug target remain incompletely understood, largely because of a lack of optimized pharmacological tools. We developed MK-8722, a potent, direct, allosteric activator of all 12 mammalian AMPK complexes. In rodents and rhesus monkeys, MK-8722-mediated AMPK activation in skeletal muscle induced robust, durable, insulin-independent glucose uptake and glycogen synthesis, with resultant improvements in glycemia and no evidence of hypoglycemia. These effects translated across species, including diabetic rhesus monkeys, but manifested with concomitant cardiac hypertrophy and increased cardiac glycogen without apparent functional sequelae.
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