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Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?

Decreases in muscle size and function are a general consequence of old age; the precise mechanisms of these changes remain unclear. Recent studies suggest that fat deposition in muscle may also contribute to dysfunction in older adults. Fat content was quantified in the quadriceps, and its effects o...

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Autores principales: Gordon III, Joseph, Remillard, Nicholas, Straight, Chad, Nagarajan, Rajakumar, Damon, Bruce, Chipkin, Stuart, Miller, Mark, Kent, Jane, Gordon, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7740761/
http://dx.doi.org/10.1093/geroni/igaa057.463
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author Gordon III, Joseph
Remillard, Nicholas
Straight, Chad
Nagarajan, Rajakumar
Damon, Bruce
Chipkin, Stuart
Miller, Mark
Kent, Jane
Gordon, Joseph
author_facet Gordon III, Joseph
Remillard, Nicholas
Straight, Chad
Nagarajan, Rajakumar
Damon, Bruce
Chipkin, Stuart
Miller, Mark
Kent, Jane
Gordon, Joseph
author_sort Gordon III, Joseph
collection PubMed
description Decreases in muscle size and function are a general consequence of old age; the precise mechanisms of these changes remain unclear. Recent studies suggest that fat deposition in muscle may also contribute to dysfunction in older adults. Fat content was quantified in the quadriceps, and its effects on function in healthy young (21-45 y) and older (65-75 y) men and women (n=44) of comparable physical activity were compared. A subset of the young matched with the older group for muscle fat content were also examined. Peak fat-free whole muscle cross-sectional area (mCSA; cm2), volume (MV; cm3), fat content (fat fraction, FF; %), specific torque (Nm/mCSA) and peak contraction velocity (Nm∙s-1) were determined using fat-water magnetic resonance imaging and dynamometry (0-300□∙s-1). To examine potential molecular mechanisms of muscle weakness, vastus lateralis biopsies were obtained (n=31) and cross-bridge kinetics of type I and II fibers were determined. FF was higher in older adults than young (8.4±1.2% (SE), 7.6±1.4; p=0.03), while mCSA (48.9±10.4 vs. 64.2±17.3), MV (1536±532 vs. 2112±708), specific torque (2.6±0.4 vs. 3.2±0.4), and peak voluntary contraction velocity (422±20 vs. 441±23) were lower in older than young (p<0.01). Type II fiber myosin attachment rate was slower and attachment time longer in older muscle (p<0.017), providing a potential mechanism for the slowing of peak contraction velocity with age. Notably, differences at the whole muscle and molecular levels remained for the subset of young and older groups matched for FF, suggesting that fat deposition in muscle does not exacerbate age-related changes in function.
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spelling pubmed-77407612020-12-21 Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content? Gordon III, Joseph Remillard, Nicholas Straight, Chad Nagarajan, Rajakumar Damon, Bruce Chipkin, Stuart Miller, Mark Kent, Jane Gordon, Joseph Innov Aging Abstracts Decreases in muscle size and function are a general consequence of old age; the precise mechanisms of these changes remain unclear. Recent studies suggest that fat deposition in muscle may also contribute to dysfunction in older adults. Fat content was quantified in the quadriceps, and its effects on function in healthy young (21-45 y) and older (65-75 y) men and women (n=44) of comparable physical activity were compared. A subset of the young matched with the older group for muscle fat content were also examined. Peak fat-free whole muscle cross-sectional area (mCSA; cm2), volume (MV; cm3), fat content (fat fraction, FF; %), specific torque (Nm/mCSA) and peak contraction velocity (Nm∙s-1) were determined using fat-water magnetic resonance imaging and dynamometry (0-300□∙s-1). To examine potential molecular mechanisms of muscle weakness, vastus lateralis biopsies were obtained (n=31) and cross-bridge kinetics of type I and II fibers were determined. FF was higher in older adults than young (8.4±1.2% (SE), 7.6±1.4; p=0.03), while mCSA (48.9±10.4 vs. 64.2±17.3), MV (1536±532 vs. 2112±708), specific torque (2.6±0.4 vs. 3.2±0.4), and peak voluntary contraction velocity (422±20 vs. 441±23) were lower in older than young (p<0.01). Type II fiber myosin attachment rate was slower and attachment time longer in older muscle (p<0.017), providing a potential mechanism for the slowing of peak contraction velocity with age. Notably, differences at the whole muscle and molecular levels remained for the subset of young and older groups matched for FF, suggesting that fat deposition in muscle does not exacerbate age-related changes in function. Oxford University Press 2020-12-16 /pmc/articles/PMC7740761/ http://dx.doi.org/10.1093/geroni/igaa057.463 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Gordon III, Joseph
Remillard, Nicholas
Straight, Chad
Nagarajan, Rajakumar
Damon, Bruce
Chipkin, Stuart
Miller, Mark
Kent, Jane
Gordon, Joseph
Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title_full Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title_fullStr Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title_full_unstemmed Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title_short Age-Related Changes in Molecular and Whole Muscle Function: Role of Fat Content?
title_sort age-related changes in molecular and whole muscle function: role of fat content?
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7740761/
http://dx.doi.org/10.1093/geroni/igaa057.463
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