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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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