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The metabolomic signature of extreme longevity: naked mole rats versus mice
The naked mole-rat (Heterocephalus glaber) is characterized by a more than tenfold higher life expectancy compared to another rodent species of the same size, namely, the laboratory mouse (Mus musculus). We used mass spectrometric metabolomics to analyze circulating plasma metabolites in both specie...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682510/ https://www.ncbi.nlm.nih.gov/pubmed/31346149 http://dx.doi.org/10.18632/aging.102116 |
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author | Viltard, Mélanie Durand, Sylvère Pérez-Lanzón, Maria Aprahamian, Fanny Lefevre, Deborah Leroy, Christine Madeo, Frank Kroemer, Guido Friedlander, Gérard |
author_facet | Viltard, Mélanie Durand, Sylvère Pérez-Lanzón, Maria Aprahamian, Fanny Lefevre, Deborah Leroy, Christine Madeo, Frank Kroemer, Guido Friedlander, Gérard |
author_sort | Viltard, Mélanie |
collection | PubMed |
description | The naked mole-rat (Heterocephalus glaber) is characterized by a more than tenfold higher life expectancy compared to another rodent species of the same size, namely, the laboratory mouse (Mus musculus). We used mass spectrometric metabolomics to analyze circulating plasma metabolites in both species at different ages. Interspecies differences were much more pronounced than age-associated alterations in the metabolome. Such interspecies divergences affected multiple metabolic pathways involving amino, bile and fatty acids as well as monosaccharides and nucleotides. The most intriguing metabolites were those that had previously been linked to pro-health and antiaging effects in mice and that were significantly increased in the long-lived rodent compared to its short-lived counterpart. This pattern applies to α-tocopherol (also known as vitamin E) and polyamines (in particular cadaverine, N8-acetylspermidine and N1,N8-diacetylspermidine), all of which were more abundant in naked mole-rats than in mice. Moreover, the age-associated decline in spermidine and N1-acetylspermidine levels observed in mice did not occur, or is even reversed (in the case of N1-acetylspermidine) in naked mole-rats. In short, the present metabolomics analysis provides a series of testable hypotheses to explain the exceptional longevity of naked mole-rats. |
format | Online Article Text |
id | pubmed-6682510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-66825102019-08-19 The metabolomic signature of extreme longevity: naked mole rats versus mice Viltard, Mélanie Durand, Sylvère Pérez-Lanzón, Maria Aprahamian, Fanny Lefevre, Deborah Leroy, Christine Madeo, Frank Kroemer, Guido Friedlander, Gérard Aging (Albany NY) Priority Research Paper The naked mole-rat (Heterocephalus glaber) is characterized by a more than tenfold higher life expectancy compared to another rodent species of the same size, namely, the laboratory mouse (Mus musculus). We used mass spectrometric metabolomics to analyze circulating plasma metabolites in both species at different ages. Interspecies differences were much more pronounced than age-associated alterations in the metabolome. Such interspecies divergences affected multiple metabolic pathways involving amino, bile and fatty acids as well as monosaccharides and nucleotides. The most intriguing metabolites were those that had previously been linked to pro-health and antiaging effects in mice and that were significantly increased in the long-lived rodent compared to its short-lived counterpart. This pattern applies to α-tocopherol (also known as vitamin E) and polyamines (in particular cadaverine, N8-acetylspermidine and N1,N8-diacetylspermidine), all of which were more abundant in naked mole-rats than in mice. Moreover, the age-associated decline in spermidine and N1-acetylspermidine levels observed in mice did not occur, or is even reversed (in the case of N1-acetylspermidine) in naked mole-rats. In short, the present metabolomics analysis provides a series of testable hypotheses to explain the exceptional longevity of naked mole-rats. Impact Journals 2019-07-24 /pmc/articles/PMC6682510/ /pubmed/31346149 http://dx.doi.org/10.18632/aging.102116 Text en Copyright © 2019 Viltard et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Priority Research Paper Viltard, Mélanie Durand, Sylvère Pérez-Lanzón, Maria Aprahamian, Fanny Lefevre, Deborah Leroy, Christine Madeo, Frank Kroemer, Guido Friedlander, Gérard The metabolomic signature of extreme longevity: naked mole rats versus mice |
title | The metabolomic signature of extreme longevity: naked mole rats versus mice |
title_full | The metabolomic signature of extreme longevity: naked mole rats versus mice |
title_fullStr | The metabolomic signature of extreme longevity: naked mole rats versus mice |
title_full_unstemmed | The metabolomic signature of extreme longevity: naked mole rats versus mice |
title_short | The metabolomic signature of extreme longevity: naked mole rats versus mice |
title_sort | metabolomic signature of extreme longevity: naked mole rats versus mice |
topic | Priority Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682510/ https://www.ncbi.nlm.nih.gov/pubmed/31346149 http://dx.doi.org/10.18632/aging.102116 |
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