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Mitochondrial determinants of mammalian longevity
Current ageing theories are far from satisfactory because of the many determinants involved in ageing. The well-known rate-of-living theory assumes that the product (lifetime energy expenditure, LEE) of maximum lifespan (MLS) and mass-specific basal metabolic rate (msBMR) is approximately constant....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666079/ https://www.ncbi.nlm.nih.gov/pubmed/29070610 http://dx.doi.org/10.1098/rsob.170083 |
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author | Kitazoe, Yasuhiro Hasegawa, Masami Tanaka, Masashi Futami, Midori Futami, Junichiro |
author_facet | Kitazoe, Yasuhiro Hasegawa, Masami Tanaka, Masashi Futami, Midori Futami, Junichiro |
author_sort | Kitazoe, Yasuhiro |
collection | PubMed |
description | Current ageing theories are far from satisfactory because of the many determinants involved in ageing. The well-known rate-of-living theory assumes that the product (lifetime energy expenditure, LEE) of maximum lifespan (MLS) and mass-specific basal metabolic rate (msBMR) is approximately constant. Although this theory provides a significant inverse correlation between msBMR and MLS as a whole for mammals, it remains problematic for two reasons. First, several interspecies studies within respective orders (typically within rodents) have shown no inverse relationships between msBMR and MLS. Second, LEE values widely vary in mammals and birds. Here, to solve these two problems, we introduced a new quantity designated as mitochondrial (mt) lifetime energy output, mtLEO = MLS × mtMR, in place of LEE, by using the mt metabolic rate (mtMR) per mitochondrion. Thereby, we found that mtLEO values were distributed more narrowly than LEE ones, and strongly correlated with the four amino-acid variables (AAVs) of Ser, Thr and Cys contents and hydrophobicity of mtDNA-encoded membrane proteins (these variables were related to the stability of these proteins). Consequently, only these two mt items, mtMR and the AAVs, solved the above-mentioned problems in the rate-of-living theory, and thus extensively improved the correlation with MLS compared with that given by LEE. |
format | Online Article Text |
id | pubmed-5666079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56660792017-11-15 Mitochondrial determinants of mammalian longevity Kitazoe, Yasuhiro Hasegawa, Masami Tanaka, Masashi Futami, Midori Futami, Junichiro Open Biol Research Current ageing theories are far from satisfactory because of the many determinants involved in ageing. The well-known rate-of-living theory assumes that the product (lifetime energy expenditure, LEE) of maximum lifespan (MLS) and mass-specific basal metabolic rate (msBMR) is approximately constant. Although this theory provides a significant inverse correlation between msBMR and MLS as a whole for mammals, it remains problematic for two reasons. First, several interspecies studies within respective orders (typically within rodents) have shown no inverse relationships between msBMR and MLS. Second, LEE values widely vary in mammals and birds. Here, to solve these two problems, we introduced a new quantity designated as mitochondrial (mt) lifetime energy output, mtLEO = MLS × mtMR, in place of LEE, by using the mt metabolic rate (mtMR) per mitochondrion. Thereby, we found that mtLEO values were distributed more narrowly than LEE ones, and strongly correlated with the four amino-acid variables (AAVs) of Ser, Thr and Cys contents and hydrophobicity of mtDNA-encoded membrane proteins (these variables were related to the stability of these proteins). Consequently, only these two mt items, mtMR and the AAVs, solved the above-mentioned problems in the rate-of-living theory, and thus extensively improved the correlation with MLS compared with that given by LEE. The Royal Society 2017-10-25 /pmc/articles/PMC5666079/ /pubmed/29070610 http://dx.doi.org/10.1098/rsob.170083 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Kitazoe, Yasuhiro Hasegawa, Masami Tanaka, Masashi Futami, Midori Futami, Junichiro Mitochondrial determinants of mammalian longevity |
title | Mitochondrial determinants of mammalian longevity |
title_full | Mitochondrial determinants of mammalian longevity |
title_fullStr | Mitochondrial determinants of mammalian longevity |
title_full_unstemmed | Mitochondrial determinants of mammalian longevity |
title_short | Mitochondrial determinants of mammalian longevity |
title_sort | mitochondrial determinants of mammalian longevity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666079/ https://www.ncbi.nlm.nih.gov/pubmed/29070610 http://dx.doi.org/10.1098/rsob.170083 |
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