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Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training

The striated activator of rho‐signaling (STARS) protein acts as a link between external stimuli and exercise adaptation such as muscle hypertrophy. However, the acute and long‐term adaptational response of STARS is still unclear. This study aimed at investigating the acute and long‐term endurance tr...

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Autores principales: Reitzner, Stefan M., Norrbom, Jessica, Sundberg, Carl Johan, Gidlund, Eva‐Karin
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/PMC5835521/
https://www.ncbi.nlm.nih.gov/pubmed/29504288
http://dx.doi.org/10.14814/phy2.13624
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author Reitzner, Stefan M.
Norrbom, Jessica
Sundberg, Carl Johan
Gidlund, Eva‐Karin
author_facet Reitzner, Stefan M.
Norrbom, Jessica
Sundberg, Carl Johan
Gidlund, Eva‐Karin
author_sort Reitzner, Stefan M.
collection PubMed
description The striated activator of rho‐signaling (STARS) protein acts as a link between external stimuli and exercise adaptation such as muscle hypertrophy. However, the acute and long‐term adaptational response of STARS is still unclear. This study aimed at investigating the acute and long‐term endurance training response on the mRNA and protein expression of STARS and its related upstream and downstream factors in human skeletal muscle. mRNA and protein levels of STARS and related factors were assessed in skeletal muscle of healthy young men and women following an acute bout of endurance exercise (n = 15) or 12 weeks of one‐legged training (n = 23). Muscle biopsies were obtained before (acute and long‐term), at 30 min, 2, and 6 h following acute exercise, and at 24 h following both acute exercise and long‐term training. Following acute exercise, STARS mRNA was significantly elevated 3.9‐fold at 30 min returning back to baseline 24 h after exercise. STARS protein levels were numerically but nonsignificantly increased 7.2‐fold at 24 h. No changes in STARS or ERR α mRNA or STARS protein expression were seen following long‐term training. PGC‐1α mRNA increased 1.7‐fold following long‐term training. MRTF‐A mRNA was increased both following acute exercise and long‐term training, in contrast to SRF mRNA and protein which did not change. STARS mRNA is acutely upregulated with exercise, but there is no cumulative effect to long‐term training as seen in PGC‐1α mRNA expression. Exercise intensity might play a role in manifestation of protein expression, suggesting a more complex regulation of STARS.
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spelling pubmed-58355212018-03-07 Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training Reitzner, Stefan M. Norrbom, Jessica Sundberg, Carl Johan Gidlund, Eva‐Karin Physiol Rep Original Research The striated activator of rho‐signaling (STARS) protein acts as a link between external stimuli and exercise adaptation such as muscle hypertrophy. However, the acute and long‐term adaptational response of STARS is still unclear. This study aimed at investigating the acute and long‐term endurance training response on the mRNA and protein expression of STARS and its related upstream and downstream factors in human skeletal muscle. mRNA and protein levels of STARS and related factors were assessed in skeletal muscle of healthy young men and women following an acute bout of endurance exercise (n = 15) or 12 weeks of one‐legged training (n = 23). Muscle biopsies were obtained before (acute and long‐term), at 30 min, 2, and 6 h following acute exercise, and at 24 h following both acute exercise and long‐term training. Following acute exercise, STARS mRNA was significantly elevated 3.9‐fold at 30 min returning back to baseline 24 h after exercise. STARS protein levels were numerically but nonsignificantly increased 7.2‐fold at 24 h. No changes in STARS or ERR α mRNA or STARS protein expression were seen following long‐term training. PGC‐1α mRNA increased 1.7‐fold following long‐term training. MRTF‐A mRNA was increased both following acute exercise and long‐term training, in contrast to SRF mRNA and protein which did not change. STARS mRNA is acutely upregulated with exercise, but there is no cumulative effect to long‐term training as seen in PGC‐1α mRNA expression. Exercise intensity might play a role in manifestation of protein expression, suggesting a more complex regulation of STARS. John Wiley and Sons Inc. 2018-03-04 /pmc/articles/PMC5835521/ /pubmed/29504288 http://dx.doi.org/10.14814/phy2.13624 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
Reitzner, Stefan M.
Norrbom, Jessica
Sundberg, Carl Johan
Gidlund, Eva‐Karin
Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title_full Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title_fullStr Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title_full_unstemmed Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title_short Expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
title_sort expression of striated activator of rho‐signaling in human skeletal muscle following acute exercise and long‐term training
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835521/
https://www.ncbi.nlm.nih.gov/pubmed/29504288
http://dx.doi.org/10.14814/phy2.13624
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