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Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats

We examined the molecular and metabolomic effects of voluntary running wheel activity in late middle-aged male Sprague Dawley rats (16–17 months). Rats were assigned either continuous voluntary running wheel access for 8 weeks (RW+) or cage-matched without running wheel access (RW−). The 9 RW+ rats...

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Autores principales: Garvey, Sean M, Russ, David W, Skelding, Mary B, Dugle, Janis E, Edens, Neile K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393218/
https://www.ncbi.nlm.nih.gov/pubmed/25716928
http://dx.doi.org/10.14814/phy2.12319
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author Garvey, Sean M
Russ, David W
Skelding, Mary B
Dugle, Janis E
Edens, Neile K
author_facet Garvey, Sean M
Russ, David W
Skelding, Mary B
Dugle, Janis E
Edens, Neile K
author_sort Garvey, Sean M
collection PubMed
description We examined the molecular and metabolomic effects of voluntary running wheel activity in late middle-aged male Sprague Dawley rats (16–17 months). Rats were assigned either continuous voluntary running wheel access for 8 weeks (RW+) or cage-matched without running wheel access (RW−). The 9 RW+ rats averaged 83 m/day (range: 8–163 m), yet exhibited both 84% reduced individual body weight gain (4.3 g vs. 26.3 g, P = 0.02) and 6.5% reduced individual average daily food intake (20.6 g vs. 22.0 g, P = 0.09) over the 8 weeks. Hindlimb muscles were harvested following an overnight fast. Muscle weights and myofiber cross-sectional area showed no difference between groups. Western blots of gastrocnemius muscle lysates with a panel of antibodies suggest that running wheel activity improved oxidative metabolism (53% increase in PGC1α, P = 0.03), increased autophagy (36% increase in LC3B-II/-I ratio, P = 0.03), and modulated growth signaling (26% increase in myostatin, P = 0.04). RW+ muscle also showed 43% increased glycogen phosphorylase expression (P = 0.04) and 45% increased glycogen content (P = 0.04). Metabolomic profiling of plantaris and soleus muscles indicated that even low-volume voluntary running wheel activity is associated with decreases in many long-chain fatty acids (e.g., palmitoleate, myristoleate, and eicosatrienoate) relative to RW− rats. Relative increases in acylcarnitines and acyl glycerophospholipids were also observed in RW+ plantaris. These data establish that even modest amounts of physical activity during late middle-age promote extensive metabolic remodeling of skeletal muscle.
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spelling pubmed-43932182015-04-20 Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats Garvey, Sean M Russ, David W Skelding, Mary B Dugle, Janis E Edens, Neile K Physiol Rep Original Research We examined the molecular and metabolomic effects of voluntary running wheel activity in late middle-aged male Sprague Dawley rats (16–17 months). Rats were assigned either continuous voluntary running wheel access for 8 weeks (RW+) or cage-matched without running wheel access (RW−). The 9 RW+ rats averaged 83 m/day (range: 8–163 m), yet exhibited both 84% reduced individual body weight gain (4.3 g vs. 26.3 g, P = 0.02) and 6.5% reduced individual average daily food intake (20.6 g vs. 22.0 g, P = 0.09) over the 8 weeks. Hindlimb muscles were harvested following an overnight fast. Muscle weights and myofiber cross-sectional area showed no difference between groups. Western blots of gastrocnemius muscle lysates with a panel of antibodies suggest that running wheel activity improved oxidative metabolism (53% increase in PGC1α, P = 0.03), increased autophagy (36% increase in LC3B-II/-I ratio, P = 0.03), and modulated growth signaling (26% increase in myostatin, P = 0.04). RW+ muscle also showed 43% increased glycogen phosphorylase expression (P = 0.04) and 45% increased glycogen content (P = 0.04). Metabolomic profiling of plantaris and soleus muscles indicated that even low-volume voluntary running wheel activity is associated with decreases in many long-chain fatty acids (e.g., palmitoleate, myristoleate, and eicosatrienoate) relative to RW− rats. Relative increases in acylcarnitines and acyl glycerophospholipids were also observed in RW+ plantaris. These data establish that even modest amounts of physical activity during late middle-age promote extensive metabolic remodeling of skeletal muscle. BlackWell Publishing Ltd 2015-02-25 /pmc/articles/PMC4393218/ /pubmed/25716928 http://dx.doi.org/10.14814/phy2.12319 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Garvey, Sean M
Russ, David W
Skelding, Mary B
Dugle, Janis E
Edens, Neile K
Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title_full Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title_fullStr Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title_full_unstemmed Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title_short Molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
title_sort molecular and metabolomic effects of voluntary running wheel activity on skeletal muscle in late middle-aged rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393218/
https://www.ncbi.nlm.nih.gov/pubmed/25716928
http://dx.doi.org/10.14814/phy2.12319
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