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NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity

BACKGROUND: NAD(+ )is a coenzyme for hydride transfer enzymes and a substrate for sirtuins and other NAD(+)-dependent ADPribose transfer enzymes. In wild-type Saccharomyces cerevisiae, calorie restriction accomplished by glucose limitation extends replicative lifespan in a manner that depends on Sir...

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Detalles Bibliográficos
Autores principales: Evans, Charles, Bogan, Katrina L, Song, Peng, Burant, Charles F, Kennedy, Robert T, Brenner, Charles
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834649/
https://www.ncbi.nlm.nih.gov/pubmed/20175898
http://dx.doi.org/10.1186/1472-6769-10-2
Descripción
Sumario:BACKGROUND: NAD(+ )is a coenzyme for hydride transfer enzymes and a substrate for sirtuins and other NAD(+)-dependent ADPribose transfer enzymes. In wild-type Saccharomyces cerevisiae, calorie restriction accomplished by glucose limitation extends replicative lifespan in a manner that depends on Sir2 and the NAD(+ )salvage enzymes, nicotinic acid phosphoribosyl transferase and nicotinamidase. Though alterations in the NAD(+ )to nicotinamide ratio and the NAD(+ )to NADH ratio are anticipated by models to account for the effects of calorie restriction, the nature of a putative change in NAD(+ )metabolism requires analytical definition and quantification of the key metabolites. RESULTS: Hydrophilic interaction chromatography followed by tandem electrospray mass spectrometry were used to identify the 12 compounds that constitute the core NAD(+ )metabolome and 6 related nucleosides and nucleotides. Whereas yeast extract and nicotinic acid increase net NAD(+ )synthesis in a manner that can account for extended lifespan, glucose restriction does not alter NAD(+ )or nicotinamide levels in ways that would increase Sir2 activity. CONCLUSIONS: The results constrain the possible mechanisms by which calorie restriction may regulate Sir2 and suggest that provision of vitamins and calorie restriction extend lifespan by different mechanisms.