SIRT1 Is Required for AMPK Activation and the Beneficial Effects of Resveratrol on Mitochondrial Function

被引:1337
作者
Price, Nathan L. [1 ]
Gomes, Ana P. [1 ,2 ]
Ling, Alvin J. Y. [1 ]
Duarte, Filipe V. [2 ]
Martin-Montalvo, Alejandro [3 ]
North, Brian J. [1 ]
Agarwal, Beamon [5 ]
Ye, Lan [5 ]
Ramadori, Giorgio [6 ]
Teodoro, Joao S. [2 ]
Hubbard, Basil P. [1 ]
Varela, Ana T. [2 ]
Davis, James G. [5 ]
Varamini, Behzad [5 ]
Hafner, Angela [1 ]
Moaddel, Ruin [4 ]
Rolo, Anabela P. [2 ,7 ]
Coppari, Roberto [6 ,8 ]
Palmeira, Carlos M. [2 ,9 ]
de Cabo, Rafael [3 ]
Baur, Joseph A. [5 ]
Sinclair, David A. [1 ,10 ]
机构
[1] Harvard Univ, Sch Med, Glenn Labs Biol Mech Aging, Boston, MA 02115 USA
[2] Ctr Neurosci & Cell Biol, P-3004517 Coimbra, Portugal
[3] NIA, Lab Expt Gerontol, NIH, Baltimore, MD 21224 USA
[4] NIA, Lab Clin Invest, NIH, Baltimore, MD 21224 USA
[5] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[6] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hypothalam Res, Dallas, TX 75390 USA
[7] Univ Aveiro, Dept Biol, P-3810193 Aveiro, Portugal
[8] Univ Politecn Marche, Dipartimento Med Sperimentale & Clin, I-60020 Ancona, Italy
[9] Univ Coimbra, Fac Sci & Technol, Dept Life Sci, P-3004517 Coimbra, Portugal
[10] Univ New S Wales, Lowy Canc Res Ctr, Dept Pharmacol, Sydney, NSW 2052, Australia
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
HIGH-FAT DIET; PROTEIN-KINASE ACTIVATION; SMALL-MOLECULE ACTIVATORS; CALORIE RESTRICTION; SKELETAL-MUSCLE; ENDOTHELIAL-CELLS; GENE-EXPRESSION; LIFE-SPAN; INSULIN SENSITIVITY; ENERGY-EXPENDITURE;
D O I
10.1016/j.cmet.2012.04.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Resveratrol induces mitochondrial biogenesis and protects against metabolic decline, but whether SIRT1 mediates these benefits is the subject of debate. To circumvent the developmental defects of germline SIRT1 knockouts, we have developed an inducible system that permits whole-body deletion of SIRT1 in adult mice. Mice treated with a moderate dose of resveratrol showed increased mitochondrial biogenesis and function, AMPK activation, and increased NAD(+) levels in skeletal muscle, whereas SIRT1 knockouts displayed none of these benefits. A mouse overexpressing SIRT1 mimicked these effects. A high dose of resveratrol activated AMPK in a SIRT1-independent manner, demonstrating that resveratrol dosage is a critical factor. Importantly, at both doses of resveratrol no improvements in mitochondrial function were observed in animals lacking SIRT1. Together these data indicate that SIRT1 plays an essential role in the ability of moderate doses of resveratrol to stimulate AMPK and improve mitochondrial function both in vitro and in vivo.
引用
收藏
页码:675 / 690
页数:16
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