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Effects of alcohol on skeletal muscle contractile performance in male and female mice

BACKGROUND: Acute and chronic alcohol use can cause skeletal muscle myopathy in concert with impairments in skeletal muscle strength, function and fatigue resistance. However, the fundamental contractile deficits induced in the presence of alcohol versus those observed in the recovery period followi...

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Autores principales: Laudato, Joseph A., Tice, Abigail L., Call, Jarrod A., Gordon, Bradley S., Steiner, Jennifer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360553/
https://www.ncbi.nlm.nih.gov/pubmed/34383848
http://dx.doi.org/10.1371/journal.pone.0255946
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author Laudato, Joseph A.
Tice, Abigail L.
Call, Jarrod A.
Gordon, Bradley S.
Steiner, Jennifer L.
author_facet Laudato, Joseph A.
Tice, Abigail L.
Call, Jarrod A.
Gordon, Bradley S.
Steiner, Jennifer L.
author_sort Laudato, Joseph A.
collection PubMed
description BACKGROUND: Acute and chronic alcohol use can cause skeletal muscle myopathy in concert with impairments in skeletal muscle strength, function and fatigue resistance. However, the fundamental contractile deficits induced in the presence of alcohol versus those observed in the recovery period following the clearance of alcohol have not yet been characterized nor is it known whether sex influences these outcomes. METHODS: Male and female mice received an intraperitoneal injection of either saline (Control) or ethanol (EtOH; 5g/kg body weight). Muscle force, fatigue, fatigue recovery and twitch characteristics of the posterior crural muscle complex were measured in situ 1 hour and 24 hours post alcohol. RESULTS: In the presence of alcohol (1-hour post treatment) absolute and normalized force generated at 80–150 Hertz was decreased in male and female mice with concurrent reductions in the rate of force development and increases in ½ relaxation time. When expressed as a percentage of maximum force, both males and females also displayed an alcohol-induced leftward shift in the force frequency curve indicative of a type I contractile phenotype. Alcohol enhanced fatigue in both males and females but had no effect on force recovery. Following clearance of alcohol (24-hour post treatment), contractile function was completely restored in females while alcohol treated males experienced sustained reductions in absolute force and had enhanced fatigue compared with male controls. CONCLUSIONS: In the presence of alcohol, both males and females exhibited significant declines in muscle force production and enhanced fatigue; however, following complete clearance of the alcohol, females recovered all functional parameters, while males did not.
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spelling pubmed-83605532021-08-13 Effects of alcohol on skeletal muscle contractile performance in male and female mice Laudato, Joseph A. Tice, Abigail L. Call, Jarrod A. Gordon, Bradley S. Steiner, Jennifer L. PLoS One Research Article BACKGROUND: Acute and chronic alcohol use can cause skeletal muscle myopathy in concert with impairments in skeletal muscle strength, function and fatigue resistance. However, the fundamental contractile deficits induced in the presence of alcohol versus those observed in the recovery period following the clearance of alcohol have not yet been characterized nor is it known whether sex influences these outcomes. METHODS: Male and female mice received an intraperitoneal injection of either saline (Control) or ethanol (EtOH; 5g/kg body weight). Muscle force, fatigue, fatigue recovery and twitch characteristics of the posterior crural muscle complex were measured in situ 1 hour and 24 hours post alcohol. RESULTS: In the presence of alcohol (1-hour post treatment) absolute and normalized force generated at 80–150 Hertz was decreased in male and female mice with concurrent reductions in the rate of force development and increases in ½ relaxation time. When expressed as a percentage of maximum force, both males and females also displayed an alcohol-induced leftward shift in the force frequency curve indicative of a type I contractile phenotype. Alcohol enhanced fatigue in both males and females but had no effect on force recovery. Following clearance of alcohol (24-hour post treatment), contractile function was completely restored in females while alcohol treated males experienced sustained reductions in absolute force and had enhanced fatigue compared with male controls. CONCLUSIONS: In the presence of alcohol, both males and females exhibited significant declines in muscle force production and enhanced fatigue; however, following complete clearance of the alcohol, females recovered all functional parameters, while males did not. Public Library of Science 2021-08-12 /pmc/articles/PMC8360553/ /pubmed/34383848 http://dx.doi.org/10.1371/journal.pone.0255946 Text en © 2021 Laudato et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Laudato, Joseph A.
Tice, Abigail L.
Call, Jarrod A.
Gordon, Bradley S.
Steiner, Jennifer L.
Effects of alcohol on skeletal muscle contractile performance in male and female mice
title Effects of alcohol on skeletal muscle contractile performance in male and female mice
title_full Effects of alcohol on skeletal muscle contractile performance in male and female mice
title_fullStr Effects of alcohol on skeletal muscle contractile performance in male and female mice
title_full_unstemmed Effects of alcohol on skeletal muscle contractile performance in male and female mice
title_short Effects of alcohol on skeletal muscle contractile performance in male and female mice
title_sort effects of alcohol on skeletal muscle contractile performance in male and female mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360553/
https://www.ncbi.nlm.nih.gov/pubmed/34383848
http://dx.doi.org/10.1371/journal.pone.0255946
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