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Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans
To test the hypothesis that a system’s metabolic rate and the complexity of fluctuations in the output of that system are related, thirteen healthy participants performed intermittent isometric knee extensor contractions at intensities where a rise in metabolic rate would (40% maximal voluntary cont...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759514/ https://www.ncbi.nlm.nih.gov/pubmed/31552708 http://dx.doi.org/10.14814/phy2.14240 |
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author | Pethick, Jamie Winter, Samantha L. Burnley, Mark |
author_facet | Pethick, Jamie Winter, Samantha L. Burnley, Mark |
author_sort | Pethick, Jamie |
collection | PubMed |
description | To test the hypothesis that a system’s metabolic rate and the complexity of fluctuations in the output of that system are related, thirteen healthy participants performed intermittent isometric knee extensor contractions at intensities where a rise in metabolic rate would (40% maximal voluntary contraction, MVC) and would not (20% MVC) be expected. The contractions had a 60% duty factor (6 sec contraction, 4 sec rest) and were performed until task failure or for 30 min, whichever occurred sooner. Torque and surface EMG signals were sampled continuously. Complexity and fractal scaling of torque were quantified using approximate entropy (ApEn) and the detrended fluctuation analysis (DFA) α scaling exponent. Muscle metabolic rate was determined using near‐infrared spectroscopy. At 40% MVC, task failure occurred after (mean ± SD) 11.5 ± 5.2 min, whereas all participants completed 30 min of contractions at 20% MVC. Muscle metabolic rate increased significantly after 2 min at 40% MVC (2.70 ± 1.48 to 4.04 ± 1.23 %·s(‐1), P < 0.001), but not at 20% MVC. Similarly, complexity decreased significantly at 40% MVC (ApEn, 0.53 ± 0.19 to 0.15 ± 0.09; DFA α, 1.37 ± 0.08 to 1.60 ± 0.09; both P < 0.001), but not at 20% MVC. The rates of change of torque complexity and muscle metabolic rate at 40% MVC were significantly correlated (ApEn, ρ = −0.63, P = 0.022; DFA, ρ = 0.58, P = 0.037). This study demonstrated that an inverse relationship exists between muscle torque complexity and metabolic rate during high‐intensity contractions. |
format | Online Article Text |
id | pubmed-6759514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67595142019-09-30 Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans Pethick, Jamie Winter, Samantha L. Burnley, Mark Physiol Rep Original Research To test the hypothesis that a system’s metabolic rate and the complexity of fluctuations in the output of that system are related, thirteen healthy participants performed intermittent isometric knee extensor contractions at intensities where a rise in metabolic rate would (40% maximal voluntary contraction, MVC) and would not (20% MVC) be expected. The contractions had a 60% duty factor (6 sec contraction, 4 sec rest) and were performed until task failure or for 30 min, whichever occurred sooner. Torque and surface EMG signals were sampled continuously. Complexity and fractal scaling of torque were quantified using approximate entropy (ApEn) and the detrended fluctuation analysis (DFA) α scaling exponent. Muscle metabolic rate was determined using near‐infrared spectroscopy. At 40% MVC, task failure occurred after (mean ± SD) 11.5 ± 5.2 min, whereas all participants completed 30 min of contractions at 20% MVC. Muscle metabolic rate increased significantly after 2 min at 40% MVC (2.70 ± 1.48 to 4.04 ± 1.23 %·s(‐1), P < 0.001), but not at 20% MVC. Similarly, complexity decreased significantly at 40% MVC (ApEn, 0.53 ± 0.19 to 0.15 ± 0.09; DFA α, 1.37 ± 0.08 to 1.60 ± 0.09; both P < 0.001), but not at 20% MVC. The rates of change of torque complexity and muscle metabolic rate at 40% MVC were significantly correlated (ApEn, ρ = −0.63, P = 0.022; DFA, ρ = 0.58, P = 0.037). This study demonstrated that an inverse relationship exists between muscle torque complexity and metabolic rate during high‐intensity contractions. John Wiley and Sons Inc. 2019-09-25 /pmc/articles/PMC6759514/ /pubmed/31552708 http://dx.doi.org/10.14814/phy2.14240 Text en © 2019 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 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 Pethick, Jamie Winter, Samantha L. Burnley, Mark Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title | Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title_full | Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title_fullStr | Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title_full_unstemmed | Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title_short | Relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
title_sort | relationship between muscle metabolic rate and muscle torque complexity during fatiguing intermittent isometric contractions in humans |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759514/ https://www.ncbi.nlm.nih.gov/pubmed/31552708 http://dx.doi.org/10.14814/phy2.14240 |
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