Systemic Pan-Ampk Activator Mk-8722 Improves Glucose Homeostasis But Induces Cardiac Hypertrophy

Robert W. Myers,Hong-Ping Guan, Juliann Ehrhart,Aleksandr Petrov, Srinivasa Prahalada, Effie Tozzo,Xiaodong Yang,Marc M. Kurtz,Maria Trujillo, Dinko Gonzalez Trotter,Danqing Feng,Shiyao Xu,George Eiermann,Marie A. Holahan,Daniel Rubins,Stacey Conarello,Xiaoda Niu,Sandra C. Souza, Corin Miller,Jinqi Liu,Ku Lu,Wen Feng,Ying Li,Ronald E. Painter, James A. Milligan, Huaibing He, Franklin Liu, Aimie Ogawa, Douglas Wisniewski, Rory J. Rohm, Liyang Wang, Michelle Bunzel,Ying Qian, Wei Zhu,Hongwu Wang,Bindu Bennet,Lisa LaFranco Scheuch, Guillermo E. Fernandez,Cai Li, Michael Klimas,Gaochao Zhou,Margaret van Heek,Tesfaye Biftu, Ann Weber,David E. Kelley,Nancy Thornberry,Mark D. Erion,Daniel M. Kemp,Iyassu K. Sebhat

SCIENCE(2017)

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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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