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Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue

INTRODUCTION: Neuromuscular fatigue reduces the temporal structure, or complexity, of muscle torque output, purportedly through an effect on motor unit behavior. Ischemic preconditioning (IPC), an emerging ergogenic aid, has been demonstrated to have a potent effect on muscular output and endurance....

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Autores principales: PETHICK, JAMIE, CASSELTON, CHARLOTTE, WINTER, SAMANTHA L., BURNLEY, MARK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803438/
https://www.ncbi.nlm.nih.gov/pubmed/32735115
http://dx.doi.org/10.1249/MSS.0000000000002475
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author PETHICK, JAMIE
CASSELTON, CHARLOTTE
WINTER, SAMANTHA L.
BURNLEY, MARK
author_facet PETHICK, JAMIE
CASSELTON, CHARLOTTE
WINTER, SAMANTHA L.
BURNLEY, MARK
author_sort PETHICK, JAMIE
collection PubMed
description INTRODUCTION: Neuromuscular fatigue reduces the temporal structure, or complexity, of muscle torque output, purportedly through an effect on motor unit behavior. Ischemic preconditioning (IPC), an emerging ergogenic aid, has been demonstrated to have a potent effect on muscular output and endurance. We therefore tested the hypothesis that IPC would attenuate the fatigue-induced loss of muscle torque complexity. METHODS: Ten healthy participants (6 males/4 females) performed intermittent isometric knee extension contractions (6 s contraction, 4 s rest) to task failure at 40% maximal voluntary contraction. Contractions were preceded by either IPC (three bouts of 5 min proximal thigh occlusion at 225 mm Hg, interspersed with 5 min rest) or SHAM (as IPC, but occlusion at only 20 mm Hg) treatments. Torque and EMG signals were sampled continuously. Complexity and fractal scaling were quantified using approximate entropy (ApEn) and the detrended fluctuation analysis (DFA) α scaling exponent. Muscle oxygen consumption (mV˙O(2)) was determined using near-infrared spectroscopy. RESULTS: IPC increased time to task failure by 43% ± 13% (mean ± SEM, P = 0.047). Complexity decreased in both trials (decreased ApEn, increased DFA α; both P < 0.001), although the rate of decrease was significantly lower after IPC (ApEn, −0.2 ± 0.1 vs –0.4 ± 0.1, P = 0.013; DFA α, 0.2 ± 0.1 vs 0.3 ± 0.1, P = 0.037). Similarly, the rates of increase in EMG amplitude (P = 0.022) and mV˙O(2) (P = 0.043) were significantly slower after IPC. CONCLUSION: These results suggest that the ergogenic effect of IPC observed here is of neural origin and accounts for the slowing of the rates of change in torque complexity, EMG amplitude, and mV˙O(2) as fatigue develops.
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spelling pubmed-78034382021-01-27 Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue PETHICK, JAMIE CASSELTON, CHARLOTTE WINTER, SAMANTHA L. BURNLEY, MARK Med Sci Sports Exerc Basic Sciences INTRODUCTION: Neuromuscular fatigue reduces the temporal structure, or complexity, of muscle torque output, purportedly through an effect on motor unit behavior. Ischemic preconditioning (IPC), an emerging ergogenic aid, has been demonstrated to have a potent effect on muscular output and endurance. We therefore tested the hypothesis that IPC would attenuate the fatigue-induced loss of muscle torque complexity. METHODS: Ten healthy participants (6 males/4 females) performed intermittent isometric knee extension contractions (6 s contraction, 4 s rest) to task failure at 40% maximal voluntary contraction. Contractions were preceded by either IPC (three bouts of 5 min proximal thigh occlusion at 225 mm Hg, interspersed with 5 min rest) or SHAM (as IPC, but occlusion at only 20 mm Hg) treatments. Torque and EMG signals were sampled continuously. Complexity and fractal scaling were quantified using approximate entropy (ApEn) and the detrended fluctuation analysis (DFA) α scaling exponent. Muscle oxygen consumption (mV˙O(2)) was determined using near-infrared spectroscopy. RESULTS: IPC increased time to task failure by 43% ± 13% (mean ± SEM, P = 0.047). Complexity decreased in both trials (decreased ApEn, increased DFA α; both P < 0.001), although the rate of decrease was significantly lower after IPC (ApEn, −0.2 ± 0.1 vs –0.4 ± 0.1, P = 0.013; DFA α, 0.2 ± 0.1 vs 0.3 ± 0.1, P = 0.037). Similarly, the rates of increase in EMG amplitude (P = 0.022) and mV˙O(2) (P = 0.043) were significantly slower after IPC. CONCLUSION: These results suggest that the ergogenic effect of IPC observed here is of neural origin and accounts for the slowing of the rates of change in torque complexity, EMG amplitude, and mV˙O(2) as fatigue develops. Lippincott Williams & Wilkins 2021-02 2020-07-29 /pmc/articles/PMC7803438/ /pubmed/32735115 http://dx.doi.org/10.1249/MSS.0000000000002475 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American College of Sports Medicine. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Basic Sciences
PETHICK, JAMIE
CASSELTON, CHARLOTTE
WINTER, SAMANTHA L.
BURNLEY, MARK
Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title_full Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title_fullStr Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title_full_unstemmed Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title_short Ischemic Preconditioning Blunts Loss of Knee Extensor Torque Complexity with Fatigue
title_sort ischemic preconditioning blunts loss of knee extensor torque complexity with fatigue
topic Basic Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803438/
https://www.ncbi.nlm.nih.gov/pubmed/32735115
http://dx.doi.org/10.1249/MSS.0000000000002475
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