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.

Branched-chain amino acid supplementation promotes survival and supports cardiac and skeletal muscle mitochondrial biogenesis in middle-aged mice

DOSSENA, Marta;CORSETTI, Giovanni;VALERIO, Alessandra;
2010-01-01

Abstract

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.
2010
MIUR (compresi PRIN FIRB,FISR)
LS4_4 Ageing
LS4_5 Metabolism, biological basis of metabolism related disorders
LS7_3 Pharmacology, pharmacogenomics, drug discovery and design, drug therapy
Esperti anonimi
Inglese
Internazionale
12
362
372
11
Scopus 99th percentile benchmarks compared to Physiology articles of the same age and document type; 98th percentile compared to Biochemistry; Molecular biology; Cell biology articles of the same age and document type. Field-Weighted Citation Impact 4.60 (FWCI shows how well cited this article is when compared to similar articles. A FWCI greater than 1.00 means the article is more cited than expected according to the average. It takes into account: The year of publication, Document type, and Disciplines associated with its source) Scopus, accessed May 19, 2017
ENDOTHELIAL NITRIC OXIDE SYNTHASE, LIFE SPAN, CALORIE RESTRICTION, INSULIN SENSITIVITY, OXYGEN NCONSUMPTION, DIETARY SUPPLEMENTATION
Altre Amm. Pubb. Italiane
no
12
info:eu-repo/semantics/article
262
D'Antona, G; Ragni, M; Cardile, A; Tedesco, L; Dossena, Marta; Bruttini, F; Caliaro, F; Corsetti, Giovanni; Bottinelli, R; Carruba, Mo; Valerio, Aless...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/41215
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