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An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy

Skeletal muscle plays a critical role in physical function and metabolic health. Muscle is a highly adaptable tissue that responds to resistance exercise (RE; loading) by hypertrophying, or during muscle disuse, RE mitigates muscle loss. Resistance exercise training (RET)–induced skeletal muscle hyp...

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Autores principales: LIM, CHANGHYUN, NUNES, EVERSON A., CURRIER, BRAD S., MCLEOD, JONATHAN C., THOMAS, AARON C. Q., PHILLIPS, STUART M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390238/
https://www.ncbi.nlm.nih.gov/pubmed/35389932
http://dx.doi.org/10.1249/MSS.0000000000002929
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author LIM, CHANGHYUN
NUNES, EVERSON A.
CURRIER, BRAD S.
MCLEOD, JONATHAN C.
THOMAS, AARON C. Q.
PHILLIPS, STUART M.
author_facet LIM, CHANGHYUN
NUNES, EVERSON A.
CURRIER, BRAD S.
MCLEOD, JONATHAN C.
THOMAS, AARON C. Q.
PHILLIPS, STUART M.
author_sort LIM, CHANGHYUN
collection PubMed
description Skeletal muscle plays a critical role in physical function and metabolic health. Muscle is a highly adaptable tissue that responds to resistance exercise (RE; loading) by hypertrophying, or during muscle disuse, RE mitigates muscle loss. Resistance exercise training (RET)–induced skeletal muscle hypertrophy is a product of external (e.g., RE programming, diet, some supplements) and internal variables (e.g., mechanotransduction, ribosomes, gene expression, satellite cells activity). RE is undeniably the most potent nonpharmacological external variable to stimulate the activation/suppression of internal variables linked to muscular hypertrophy or countering disuse-induced muscle loss. Here, we posit that despite considerable research on the impact of external variables on RET and hypertrophy, internal variables (i.e., inherent skeletal muscle biology) are dominant in regulating the extent of hypertrophy in response to external stimuli. Thus, identifying the key internal skeletal muscle–derived variables that mediate the translation of external RE variables will be pivotal to determining the most effective strategies for skeletal muscle hypertrophy in healthy persons. Such work will aid in enhancing function in clinical populations, slowing functional decline, and promoting physical mobility. We provide up-to-date, evidence-based perspectives of the mechanisms regulating RET-induced skeletal muscle hypertrophy.
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spelling pubmed-93902382022-08-26 An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy LIM, CHANGHYUN NUNES, EVERSON A. CURRIER, BRAD S. MCLEOD, JONATHAN C. THOMAS, AARON C. Q. PHILLIPS, STUART M. Med Sci Sports Exerc Applied Sciences Skeletal muscle plays a critical role in physical function and metabolic health. Muscle is a highly adaptable tissue that responds to resistance exercise (RE; loading) by hypertrophying, or during muscle disuse, RE mitigates muscle loss. Resistance exercise training (RET)–induced skeletal muscle hypertrophy is a product of external (e.g., RE programming, diet, some supplements) and internal variables (e.g., mechanotransduction, ribosomes, gene expression, satellite cells activity). RE is undeniably the most potent nonpharmacological external variable to stimulate the activation/suppression of internal variables linked to muscular hypertrophy or countering disuse-induced muscle loss. Here, we posit that despite considerable research on the impact of external variables on RET and hypertrophy, internal variables (i.e., inherent skeletal muscle biology) are dominant in regulating the extent of hypertrophy in response to external stimuli. Thus, identifying the key internal skeletal muscle–derived variables that mediate the translation of external RE variables will be pivotal to determining the most effective strategies for skeletal muscle hypertrophy in healthy persons. Such work will aid in enhancing function in clinical populations, slowing functional decline, and promoting physical mobility. We provide up-to-date, evidence-based perspectives of the mechanisms regulating RET-induced skeletal muscle hypertrophy. Lippincott Williams & Wilkins 2022-09 2022-04-06 /pmc/articles/PMC9390238/ /pubmed/35389932 http://dx.doi.org/10.1249/MSS.0000000000002929 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American College of Sports Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/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) (https://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 Applied Sciences
LIM, CHANGHYUN
NUNES, EVERSON A.
CURRIER, BRAD S.
MCLEOD, JONATHAN C.
THOMAS, AARON C. Q.
PHILLIPS, STUART M.
An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title_full An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title_fullStr An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title_full_unstemmed An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title_short An Evidence-Based Narrative Review of Mechanisms of Resistance Exercise–Induced Human Skeletal Muscle Hypertrophy
title_sort evidence-based narrative review of mechanisms of resistance exercise–induced human skeletal muscle hypertrophy
topic Applied Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390238/
https://www.ncbi.nlm.nih.gov/pubmed/35389932
http://dx.doi.org/10.1249/MSS.0000000000002929
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