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Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle

The aim of this study was to investigate the effects of an acute bout of eccentric actions, performed at fast velocity (210º(.)s(-1)) and at slow velocity (20º(.)s(-1)), on the gene expression of regulatory components of the myostatin (MSTN) signalling pathway. Participants performed an acute bout o...

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Autores principales: Roschel, Hamilton, Ugrinowistch, Carlos, Santos, Audrei Reis, Barbosa, Wesley Pereira, Miyabara, Elen Haruka, Tricoli, Valmor, Aoki, Marcelo Saldanha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Institute of Sport in Warsaw 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234307/
https://www.ncbi.nlm.nih.gov/pubmed/30455539
http://dx.doi.org/10.5114/biolsport.2018.71600
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author Roschel, Hamilton
Ugrinowistch, Carlos
Santos, Audrei Reis
Barbosa, Wesley Pereira
Miyabara, Elen Haruka
Tricoli, Valmor
Aoki, Marcelo Saldanha
author_facet Roschel, Hamilton
Ugrinowistch, Carlos
Santos, Audrei Reis
Barbosa, Wesley Pereira
Miyabara, Elen Haruka
Tricoli, Valmor
Aoki, Marcelo Saldanha
author_sort Roschel, Hamilton
collection PubMed
description The aim of this study was to investigate the effects of an acute bout of eccentric actions, performed at fast velocity (210º(.)s(-1)) and at slow velocity (20º(.)s(-1)), on the gene expression of regulatory components of the myostatin (MSTN) signalling pathway. Participants performed an acute bout of eccentric actions at either a slow or a fast velocity. Muscle biopsy samples were taken before, immediately after, and 2 h after the exercise bout. The gene expression of the components of the MSTN pathway was assessed by real-time PCR. No change was observed in MSTN, ACTRIIB, GASP-1 or FOXO-3a gene expression after either slow or fast eccentric actions (p > 0.05). However, the MSTN inhibitors follistatin (FST), FST-like-3 (FSTL3) and SMAD-7 were significantly increased 2 h after both eccentric actions (p < 0.05). No significant difference between bouts was found before, immediately after, or 2 h after the eccentric actions (slow and fast velocities, p > 0.05). The current findings indicate that a bout of eccentric actions activates the expression of MSTN inhibitors. However, no difference was observed in MSTN inhibitors’ gene expression when comparing slow and fast eccentric actions. It is possible that the greater time under tension induced by slow eccentric (SE) actions might compensate the effect of the greater velocity of fast eccentric (FE) actions. Additional studies are required to address the effect of eccentric action (EA) velocities on the pathways related to muscle hypertrophy.
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spelling pubmed-62343072018-11-19 Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle Roschel, Hamilton Ugrinowistch, Carlos Santos, Audrei Reis Barbosa, Wesley Pereira Miyabara, Elen Haruka Tricoli, Valmor Aoki, Marcelo Saldanha Biol Sport Original Paper The aim of this study was to investigate the effects of an acute bout of eccentric actions, performed at fast velocity (210º(.)s(-1)) and at slow velocity (20º(.)s(-1)), on the gene expression of regulatory components of the myostatin (MSTN) signalling pathway. Participants performed an acute bout of eccentric actions at either a slow or a fast velocity. Muscle biopsy samples were taken before, immediately after, and 2 h after the exercise bout. The gene expression of the components of the MSTN pathway was assessed by real-time PCR. No change was observed in MSTN, ACTRIIB, GASP-1 or FOXO-3a gene expression after either slow or fast eccentric actions (p > 0.05). However, the MSTN inhibitors follistatin (FST), FST-like-3 (FSTL3) and SMAD-7 were significantly increased 2 h after both eccentric actions (p < 0.05). No significant difference between bouts was found before, immediately after, or 2 h after the eccentric actions (slow and fast velocities, p > 0.05). The current findings indicate that a bout of eccentric actions activates the expression of MSTN inhibitors. However, no difference was observed in MSTN inhibitors’ gene expression when comparing slow and fast eccentric actions. It is possible that the greater time under tension induced by slow eccentric (SE) actions might compensate the effect of the greater velocity of fast eccentric (FE) actions. Additional studies are required to address the effect of eccentric action (EA) velocities on the pathways related to muscle hypertrophy. Institute of Sport in Warsaw 2017-11-23 2018-06 /pmc/articles/PMC6234307/ /pubmed/30455539 http://dx.doi.org/10.5114/biolsport.2018.71600 Text en Copyright © Biology of Sport 2018 http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Roschel, Hamilton
Ugrinowistch, Carlos
Santos, Audrei Reis
Barbosa, Wesley Pereira
Miyabara, Elen Haruka
Tricoli, Valmor
Aoki, Marcelo Saldanha
Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title_full Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title_fullStr Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title_full_unstemmed Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title_short Effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
title_sort effect of eccentric action velocity on expression of genes related to myostatin signaling pathway in human skeletal muscle
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234307/
https://www.ncbi.nlm.nih.gov/pubmed/30455539
http://dx.doi.org/10.5114/biolsport.2018.71600
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