Branched-Chain Amino Acid Supplementation Promotes Survival and Supports Cardiac and Skeletal Muscle Mitochondrial Biogenesis in Middle-Aged Mice

被引:476
作者
D'Antona, Giuseppe [2 ,3 ]
Ragni, Maurizio [1 ]
Cardile, Annalisa [1 ]
Tedesco, Laura [1 ,4 ]
Dossena, Marta [1 ,5 ]
Bruttini, Flavia [2 ,3 ]
Caliaro, Francesca [2 ,3 ]
Corsetti, Giovanni [6 ]
Bottinelli, Roberto [2 ,3 ]
Carruba, Michele O. [1 ,4 ]
Valerio, Alessandra [1 ,5 ]
Nisoli, Enzo [1 ,4 ]
机构
[1] Univ Milan, Sch Med, Ctr Study & Res Obes, Dept Pharmacol Chemotherapy & Med Toxicol, I-20129 Milan, Italy
[2] Univ Pavia, Human Physiol Unit, Dept Physiol, I-27100 Pavia, Italy
[3] Univ Pavia, Interuniv Inst Myol, I-27100 Pavia, Italy
[4] Ist Auxol Italiano, I-20145 Milan, Italy
[5] Univ Brescia, Pharmacol Unit, I-25123 Brescia, Italy
[6] Univ Brescia, Human Anat Unit, Dept Biomed Sci & Biotechnol, I-25123 Brescia, Italy
关键词
NITRIC-OXIDE SYNTHASE; EXTENDS LIFE-SPAN; CALORIE RESTRICTION; INSULIN SENSITIVITY; ENDOTHELIAL-CELLS; MAMMALIAN TARGET; SACCHAROMYCES-CEREVISIAE; DIETARY RESTRICTION; OXYGEN-CONSUMPTION; PROTEIN-SYNTHESIS;
D O I
10.1016/j.cmet.2010.08.016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent evidence points to a strong relationship between increased mitochondrial biogenesis and increased survival in eukaryotes. Branched-chain amino acids (BCAAs) have been shown to extend chronological life span in yeast. However, the role of these amino acids in mitochondrial biogenesis and longevity in mammals is unknown. Here, we show that a BCAA-enriched mixture (BCAAem) increased the average life span of mice. BCAAem supplementation increased mitochondrial biogenesis and sirtuin 1 expression in primary cardiac and skeletal myocytes and in cardiac and skeletal muscle, but not in adipose tissue and liver of middle-aged mice, and this was accompanied by enhanced physical endurance. Moreover, the reactive oxygen species (ROS) defense system genes were upregulated, and ROS production was reduced by BCAAem supplementation. All of the BCAAem-mediated effects were strongly attenuated in endothelial nitric oxide synthase null mutant mice. These data reveal an important antiaging role of BCAAs mediated by mitochondrial biogenesis in mammals.
引用
收藏
页码:362 / 372
页数:11
相关论文
共 61 条
[1]   Autophagy and amino acid homeostasis are required for chronological longevity in Saccharomyces cerevisiae [J].
Alvers, Ashley L. ;
Fishwick, Laura K. ;
Wood, Michael S. ;
Hu, Doreen ;
Chung, Hye S. ;
Dunn, William A., Jr. ;
Aris, John P. .
AGING CELL, 2009, 8 (04) :353-369
[2]   Amino acid regulation of TOR complex 1 [J].
Avruch, Joseph ;
Long, Xiaomeng ;
Ortiz-Vega, Sara ;
Rapley, Joseph ;
Papageorgiou, Angela ;
Dai, Ning .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2009, 296 (04) :E592-E602
[3]   In human endothelial cells rapamycin causes mTORC2 inhibition and impairs cell viability and function [J].
Barilli, Amelia ;
Visigalli, Rossana ;
Sala, Roberto ;
Gazzola, Gian C. ;
Parolari, Alessandro ;
Tremoli, Elena ;
Bonomini, Sabrina ;
Simon, Alexandra ;
Closs, Ellen I. ;
Dall'Asta, Valeria ;
Bussolati, Ovidio .
CARDIOVASCULAR RESEARCH, 2008, 78 (03) :563-571
[4]   Mitochondrial oxygen consumption and reactive oxygen species production are independently modulated: Implications for aging studies [J].
Barja, Gustavo .
REJUVENATION RESEARCH, 2007, 10 (02) :215-223
[5]   Resveratrol improves health and survival of mice on a high-calorie diet [J].
Baur, Joseph A. ;
Pearson, Kevin J. ;
Price, Nathan L. ;
Jamieson, Hamish A. ;
Lerin, Carles ;
Kalra, Avash ;
Prabhu, Vinayakumar V. ;
Allard, Joanne S. ;
Lopez-Lluch, Guillermo ;
Lewis, Kaitlyn ;
Pistell, Paul J. ;
Poosala, Suresh ;
Becker, Kevin G. ;
Boss, Olivier ;
Gwinn, Dana ;
Wang, Mingyi ;
Ramaswamy, Sharan ;
Fishbein, Kenneth W. ;
Spencer, Richard G. ;
Lakatta, Edward G. ;
Le Couteur, David ;
Shaw, Reuben J. ;
Navas, Placido ;
Puigserver, Pere ;
Ingram, Donald K. ;
de Cabo, Rafael ;
Sinclair, David A. .
NATURE, 2006, 444 (7117) :337-342
[6]   Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice [J].
Benchaouir, Rachid ;
Meregalli, Mirella ;
Farini, Andrea ;
D'Antona, Giuseppe ;
Belicchi, Marzia ;
Goyenvalle, Aurelie ;
Battistelli, Maurizio ;
Bresolin, Nereo ;
Bottinelli, Roberto ;
Garcia, Luis ;
Torrente, Yvan .
CELL STEM CELL, 2007, 1 (06) :646-657
[7]   Skeletal Muscle-Specific Ablation of raptor, but Not of rictor, Causes Metabolic Changes and Results in Muscle Dystrophy [J].
Bentzinger, C. Florian ;
Romanino, Klaas ;
Cloetta, Dimitri ;
Lin, Shuo ;
Mascarenhas, Joseph B. ;
Oliveri, Filippo ;
Xia, Jinyu ;
Casanova, Emilio ;
Costa, Celine F. ;
Brink, Marijke ;
Zorzato, Francesco ;
Hall, Michael N. ;
Rueegg, Markus A. .
CELL METABOLISM, 2008, 8 (05) :411-424
[8]   Reduced TOR signaling extends chronological life span via increased respiration and upregulation of mitochondrial gene expression [J].
Bonawitz, Nicholas D. ;
Chatenay-Lapointe, Marc ;
Pan, Yong ;
Shadel, Gerald S. .
CELL METABOLISM, 2007, 5 (04) :265-277
[9]   Tissue-specific regulation of SIRT1 by calorie restriction [J].
Chen, Danica ;
Bruno, Joanne ;
Easlon, Erin ;
Lin, Su-Ju ;
Cheng, Hwei-Ling ;
Alt, Frederick W. ;
Guarente, Leonard .
GENES & DEVELOPMENT, 2008, 22 (13) :1753-1757
[10]   Calorie restriction increases muscle mitochondrial biogenesis in healthy humans [J].
Civitarese, Anthony E. ;
Carling, Stacy ;
Heilbronn, Leonie K. ;
Hulver, Mathew H. ;
Ukropcova, Barbara ;
Deutsch, Walter A. ;
Smith, Steven R. ;
Ravussin, Eric .
PLOS MEDICINE, 2007, 4 (03) :485-494