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A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice
Aging is associated with distinct phenotypical, physiological, and functional changes, leading to disease and death. The progression of aging-related traits varies widely among individuals, influenced by their environment, lifestyle, and genetics. In this study, we conducted physiologic and function...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099423/ https://www.ncbi.nlm.nih.gov/pubmed/33876723 http://dx.doi.org/10.7554/eLife.62952 |
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author | Petr, Michael A Alfaras, Irene Krawcyzk, Melissa Bair, Woei-Nan Mitchell, Sarah J Morrell, Christopher H Studenski, Stephanie A Price, Nathan L Fishbein, Kenneth W Spencer, Richard G Scheibye-Knudsen, Morten Lakatta, Edward G Ferrucci, Luigi Aon, Miguel A Bernier, Michel de Cabo, Rafael |
author_facet | Petr, Michael A Alfaras, Irene Krawcyzk, Melissa Bair, Woei-Nan Mitchell, Sarah J Morrell, Christopher H Studenski, Stephanie A Price, Nathan L Fishbein, Kenneth W Spencer, Richard G Scheibye-Knudsen, Morten Lakatta, Edward G Ferrucci, Luigi Aon, Miguel A Bernier, Michel de Cabo, Rafael |
author_sort | Petr, Michael A |
collection | PubMed |
description | Aging is associated with distinct phenotypical, physiological, and functional changes, leading to disease and death. The progression of aging-related traits varies widely among individuals, influenced by their environment, lifestyle, and genetics. In this study, we conducted physiologic and functional tests cross-sectionally throughout the entire lifespan of male C57BL/6N mice. In parallel, metabolomics analyses in serum, brain, liver, heart, and skeletal muscle were also performed to identify signatures associated with frailty and age-dependent functional decline. Our findings indicate that declines in gait speed as a function of age and frailty are associated with a dramatic increase in the energetic cost of physical activity and decreases in working capacity. Aging and functional decline prompt organs to rewire their metabolism and substrate selection and toward redox-related pathways, mainly in liver and heart. Collectively, the data provide a framework to further understand and characterize processes of aging at the individual organism and organ levels. |
format | Online Article Text |
id | pubmed-8099423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80994232021-05-06 A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice Petr, Michael A Alfaras, Irene Krawcyzk, Melissa Bair, Woei-Nan Mitchell, Sarah J Morrell, Christopher H Studenski, Stephanie A Price, Nathan L Fishbein, Kenneth W Spencer, Richard G Scheibye-Knudsen, Morten Lakatta, Edward G Ferrucci, Luigi Aon, Miguel A Bernier, Michel de Cabo, Rafael eLife Computational and Systems Biology Aging is associated with distinct phenotypical, physiological, and functional changes, leading to disease and death. The progression of aging-related traits varies widely among individuals, influenced by their environment, lifestyle, and genetics. In this study, we conducted physiologic and functional tests cross-sectionally throughout the entire lifespan of male C57BL/6N mice. In parallel, metabolomics analyses in serum, brain, liver, heart, and skeletal muscle were also performed to identify signatures associated with frailty and age-dependent functional decline. Our findings indicate that declines in gait speed as a function of age and frailty are associated with a dramatic increase in the energetic cost of physical activity and decreases in working capacity. Aging and functional decline prompt organs to rewire their metabolism and substrate selection and toward redox-related pathways, mainly in liver and heart. Collectively, the data provide a framework to further understand and characterize processes of aging at the individual organism and organ levels. eLife Sciences Publications, Ltd 2021-04-20 /pmc/articles/PMC8099423/ /pubmed/33876723 http://dx.doi.org/10.7554/eLife.62952 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Computational and Systems Biology Petr, Michael A Alfaras, Irene Krawcyzk, Melissa Bair, Woei-Nan Mitchell, Sarah J Morrell, Christopher H Studenski, Stephanie A Price, Nathan L Fishbein, Kenneth W Spencer, Richard G Scheibye-Knudsen, Morten Lakatta, Edward G Ferrucci, Luigi Aon, Miguel A Bernier, Michel de Cabo, Rafael A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title | A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title_full | A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title_fullStr | A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title_full_unstemmed | A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title_short | A cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
title_sort | cross-sectional study of functional and metabolic changes during aging through the lifespan in male mice |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099423/ https://www.ncbi.nlm.nih.gov/pubmed/33876723 http://dx.doi.org/10.7554/eLife.62952 |
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