Cargando…
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice
The age‐related impairment in muscle function results in a drastic decline in motor coordination and mobility in elderly individuals. Regular physical activity is the only efficient intervention to prevent and treat this age‐associated degeneration. However, the mechanisms that underlie the therapeu...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770876/ https://www.ncbi.nlm.nih.gov/pubmed/29067788 http://dx.doi.org/10.1111/acel.12697 |
_version_ | 1783293152237453312 |
---|---|
author | Gill, Jonathan F. Santos, Gesa Schnyder, Svenia Handschin, Christoph |
author_facet | Gill, Jonathan F. Santos, Gesa Schnyder, Svenia Handschin, Christoph |
author_sort | Gill, Jonathan F. |
collection | PubMed |
description | The age‐related impairment in muscle function results in a drastic decline in motor coordination and mobility in elderly individuals. Regular physical activity is the only efficient intervention to prevent and treat this age‐associated degeneration. However, the mechanisms that underlie the therapeutic effect of exercise in this context remain unclear. We assessed whether endurance exercise training in old age is sufficient to affect muscle and motor function. Moreover, as muscle peroxisome proliferator‐activated receptor γ coactivator 1α (PGC‐1α) is a key regulatory hub in endurance exercise adaptation with decreased expression in old muscle, we studied the involvement of PGC‐1α in the therapeutic effect of exercise in aging. Intriguingly, PGC‐1α muscle‐specific knockout and overexpression, respectively, precipitated and alleviated specific aspects of aging‐related deterioration of muscle function in old mice, while other muscle dysfunctions remained unchanged upon PGC‐1α modulation. Surprisingly, we discovered that muscle PGC‐1α was not only involved in improving muscle endurance and mitochondrial remodeling, but also phenocopied endurance exercise training in advanced age by contributing to maintaining balance and motor coordination in old animals. Our data therefore suggest that the benefits of exercise, even when performed at old age, extend beyond skeletal muscle and are at least in part mediated by PGC‐1α. |
format | Online Article Text |
id | pubmed-5770876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57708762018-02-01 PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice Gill, Jonathan F. Santos, Gesa Schnyder, Svenia Handschin, Christoph Aging Cell Original Articles The age‐related impairment in muscle function results in a drastic decline in motor coordination and mobility in elderly individuals. Regular physical activity is the only efficient intervention to prevent and treat this age‐associated degeneration. However, the mechanisms that underlie the therapeutic effect of exercise in this context remain unclear. We assessed whether endurance exercise training in old age is sufficient to affect muscle and motor function. Moreover, as muscle peroxisome proliferator‐activated receptor γ coactivator 1α (PGC‐1α) is a key regulatory hub in endurance exercise adaptation with decreased expression in old muscle, we studied the involvement of PGC‐1α in the therapeutic effect of exercise in aging. Intriguingly, PGC‐1α muscle‐specific knockout and overexpression, respectively, precipitated and alleviated specific aspects of aging‐related deterioration of muscle function in old mice, while other muscle dysfunctions remained unchanged upon PGC‐1α modulation. Surprisingly, we discovered that muscle PGC‐1α was not only involved in improving muscle endurance and mitochondrial remodeling, but also phenocopied endurance exercise training in advanced age by contributing to maintaining balance and motor coordination in old animals. Our data therefore suggest that the benefits of exercise, even when performed at old age, extend beyond skeletal muscle and are at least in part mediated by PGC‐1α. John Wiley and Sons Inc. 2017-10-25 2018-02 /pmc/articles/PMC5770876/ /pubmed/29067788 http://dx.doi.org/10.1111/acel.12697 Text en © 2017 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Gill, Jonathan F. Santos, Gesa Schnyder, Svenia Handschin, Christoph PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title |
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title_full |
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title_fullStr |
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title_full_unstemmed |
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title_short |
PGC‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
title_sort | pgc‐1α affects aging‐related changes in muscle and motor function by modulating specific exercise‐mediated changes in old mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770876/ https://www.ncbi.nlm.nih.gov/pubmed/29067788 http://dx.doi.org/10.1111/acel.12697 |
work_keys_str_mv | AT gilljonathanf pgc1aaffectsagingrelatedchangesinmuscleandmotorfunctionbymodulatingspecificexercisemediatedchangesinoldmice AT santosgesa pgc1aaffectsagingrelatedchangesinmuscleandmotorfunctionbymodulatingspecificexercisemediatedchangesinoldmice AT schnydersvenia pgc1aaffectsagingrelatedchangesinmuscleandmotorfunctionbymodulatingspecificexercisemediatedchangesinoldmice AT handschinchristoph pgc1aaffectsagingrelatedchangesinmuscleandmotorfunctionbymodulatingspecificexercisemediatedchangesinoldmice |