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Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience

Age is the greatest risk factor for chronic disease and is associated with a marked decline in functional capacity and quality of life. A key factor contributing to loss of function in older adults is the decline in skeletal muscle function. While the exact mechanism(s) remains incompletely understo...

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Autores principales: Chung, Susie, Rosenberry, Ryan, Ryan, Terence E., Munson, Madison, Dombrowsky, Thomas, Park, Suwon, Nasirian, Aida, Haykowsky, Mark J., Nelson, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801551/
https://www.ncbi.nlm.nih.gov/pubmed/29411535
http://dx.doi.org/10.14814/phy2.13588
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author Chung, Susie
Rosenberry, Ryan
Ryan, Terence E.
Munson, Madison
Dombrowsky, Thomas
Park, Suwon
Nasirian, Aida
Haykowsky, Mark J.
Nelson, Michael D.
author_facet Chung, Susie
Rosenberry, Ryan
Ryan, Terence E.
Munson, Madison
Dombrowsky, Thomas
Park, Suwon
Nasirian, Aida
Haykowsky, Mark J.
Nelson, Michael D.
author_sort Chung, Susie
collection PubMed
description Age is the greatest risk factor for chronic disease and is associated with a marked decline in functional capacity and quality of life. A key factor contributing to loss of function in older adults is the decline in skeletal muscle function. While the exact mechanism(s) remains incompletely understood, age‐related mitochondrial dysfunction is thought to play a major role. To explore this question further, we studied 15 independently living seniors (age: 72 ± 5 years; m/f: 4/11; BMI: 27.6 ± 5.9) and 17 young volunteers (age: 25 ± 4 years; m/f: 8/9; BMI: 24.0 ± 3.3). Skeletal muscle oxidative function was measured in forearm muscle from the recovery kinetics of muscle oxygen consumption using near‐infrared spectroscopy (NIRS). Muscle oxygen consumption was calculated as the slope of change in hemoglobin saturation during a series of rapid, supra‐systolic arterial cuff occlusions following a brief bout of exercise. Aging was associated with a significant prolongation of the time constant of oxidative recovery following exercise (51.8 ± 5.4 sec vs. 37.1 ± 2.1 sec, P = 0.04, old vs. young, respectively). This finding suggests an overall reduction in mitochondrial function with age in nonlocomotor skeletal muscle. That these data were obtained using NIRS holds great promise in gerontology for quantitative assessment of skeletal muscle oxidative function at the bed side or clinic.
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spelling pubmed-58015512018-03-15 Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience Chung, Susie Rosenberry, Ryan Ryan, Terence E. Munson, Madison Dombrowsky, Thomas Park, Suwon Nasirian, Aida Haykowsky, Mark J. Nelson, Michael D. Physiol Rep Original Research Age is the greatest risk factor for chronic disease and is associated with a marked decline in functional capacity and quality of life. A key factor contributing to loss of function in older adults is the decline in skeletal muscle function. While the exact mechanism(s) remains incompletely understood, age‐related mitochondrial dysfunction is thought to play a major role. To explore this question further, we studied 15 independently living seniors (age: 72 ± 5 years; m/f: 4/11; BMI: 27.6 ± 5.9) and 17 young volunteers (age: 25 ± 4 years; m/f: 8/9; BMI: 24.0 ± 3.3). Skeletal muscle oxidative function was measured in forearm muscle from the recovery kinetics of muscle oxygen consumption using near‐infrared spectroscopy (NIRS). Muscle oxygen consumption was calculated as the slope of change in hemoglobin saturation during a series of rapid, supra‐systolic arterial cuff occlusions following a brief bout of exercise. Aging was associated with a significant prolongation of the time constant of oxidative recovery following exercise (51.8 ± 5.4 sec vs. 37.1 ± 2.1 sec, P = 0.04, old vs. young, respectively). This finding suggests an overall reduction in mitochondrial function with age in nonlocomotor skeletal muscle. That these data were obtained using NIRS holds great promise in gerontology for quantitative assessment of skeletal muscle oxidative function at the bed side or clinic. John Wiley and Sons Inc. 2018-02-07 /pmc/articles/PMC5801551/ /pubmed/29411535 http://dx.doi.org/10.14814/phy2.13588 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. 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 Research
Chung, Susie
Rosenberry, Ryan
Ryan, Terence E.
Munson, Madison
Dombrowsky, Thomas
Park, Suwon
Nasirian, Aida
Haykowsky, Mark J.
Nelson, Michael D.
Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title_full Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title_fullStr Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title_full_unstemmed Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title_short Near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
title_sort near‐infrared spectroscopy detects age‐related differences in skeletal muscle oxidative function: promising implications for geroscience
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801551/
https://www.ncbi.nlm.nih.gov/pubmed/29411535
http://dx.doi.org/10.14814/phy2.13588
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