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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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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 |
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author | Evans, Charles Bogan, Katrina L Song, Peng Burant, Charles F Kennedy, Robert T Brenner, Charles |
author_facet | Evans, Charles Bogan, Katrina L Song, Peng Burant, Charles F Kennedy, Robert T Brenner, Charles |
author_sort | Evans, Charles |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2834649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28346492010-03-09 NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity Evans, Charles Bogan, Katrina L Song, Peng Burant, Charles F Kennedy, Robert T Brenner, Charles BMC Chem Biol Research article 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. BioMed Central 2010-02-22 /pmc/articles/PMC2834649/ /pubmed/20175898 http://dx.doi.org/10.1186/1472-6769-10-2 Text en Copyright ©2010 Evans et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research article Evans, Charles Bogan, Katrina L Song, Peng Burant, Charles F Kennedy, Robert T Brenner, Charles NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title | NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title_full | NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title_fullStr | NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title_full_unstemmed | NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title_short | NAD(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
title_sort | nad(+ )metabolite levels as a function of vitamins and calorie restriction: evidence for different mechanisms of longevity |
topic | Research article |
url | 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 |
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