白藜芦醇
安普克
磷酸二酯酶
角色扮演
医学
内分泌学
药理学
内科学
生物化学
化学
蛋白激酶A
酶
作者
Sung-Jun Park,Faiyaz Ahmad,Andrew Philp,Keith Baar,Tishan Williams,Hai‐Bin Luo,Hengming Ke,Holger Rehmann,Ronald Taussig,Alexandra L. Brown,Myung K. Kim,Michael A. Beaven,Alex B. Burgin,Vincent C. Manganiello,Jay H. Chung
标识
DOI:10.1186/1753-6561-6-s3-p73
摘要
Resveratrol, a polyphenol in red wine, has been reported as a calorie restriction mimetic with potential antiaging and antidiabetogenic properties. It is widely consumed as a nutritional supplement, but its mechanism of action remains a mystery. Here, we report that the metabolic effects of resveratrol result from competitive inhibition of cAMP-degrading phosphodiesterases, leading to elevated cAMP levels. The resulting activation of Epac1, a cAMP effector protein, increases intracellular Ca2+ levels and activates the CamKKβ-AMPK pathway via phospholipase C and the ryanodine receptor Ca2+-release channel. As a consequence, resveratrol increases NAD+ and the activity of Sirt1. Inhibiting PDE4 with rolipram reproduces all of the metabolic benefits of resveratrol, including prevention of diet-induced obesity and an increase in mitochondrial function, physical stamina, and glucose tolerance in mice.
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