Cargando…

The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes

Previous studies have reported that different modes of muscle contraction (i.e., eccentric or concentric contraction) with similar contraction times can affect muscle proteolytic responses. However, the effect of different contraction modes on muscle proteolytic response under the same force−time in...

Descripción completa

Detalles Bibliográficos
Autores principales: Ato, Satoru, Makanae, Yuhei, Kido, Kohei, Sase, Kohei, Yoshii, Naomi, Fujita, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555890/
https://www.ncbi.nlm.nih.gov/pubmed/28778992
http://dx.doi.org/10.14814/phy2.13364
_version_ 1783256973577289728
author Ato, Satoru
Makanae, Yuhei
Kido, Kohei
Sase, Kohei
Yoshii, Naomi
Fujita, Satoshi
author_facet Ato, Satoru
Makanae, Yuhei
Kido, Kohei
Sase, Kohei
Yoshii, Naomi
Fujita, Satoshi
author_sort Ato, Satoru
collection PubMed
description Previous studies have reported that different modes of muscle contraction (i.e., eccentric or concentric contraction) with similar contraction times can affect muscle proteolytic responses. However, the effect of different contraction modes on muscle proteolytic response under the same force−time integral (FTI: contraction force × time) has not been investigated. The purpose of this study was to investigate the effect of different contraction modes, with the same FTI, on acute proteolytic signaling responses. Eleven‐week‐old male Sprague–Dawley rats were randomly assigned to eccentric (EC), concentric (CC), or isometric contraction (IC) groups. Different modes of muscle contraction were performed on the right gastrocnemius muscle using electrical stimulation, with the left muscle acting as a control. In order to apply an equivalent FTI, the number of stimulation sets was modified between the groups. Muscle samples were taken immediately and three hours after exercise. Phosphorylation of FoxO3a at Ser253 was significantly increased immediately after exercise compared to controls irrespective of contraction mode. The mRNA levels of the ubiquitin ligases, MuRF1, and MAFbx mRNA were unchanged by contraction mode or time. Phosphorylation of ULK1 at Ser317 (positive regulatory site) and Ser757 (negative regulatory site) was significantly increased compared to controls, immediately or 3 h after exercise, in all contraction modes. The autophagy markers (LC3B‐II/I ratio and p62 expression) were unchanged, regardless of contraction mode. These data suggest that differences in contraction mode during resistance exercise with a constant FTI, are not factors in regulating proteolytic signaling in the early phase of skeletal muscle contraction.
format Online
Article
Text
id pubmed-5555890
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-55558902017-08-16 The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes Ato, Satoru Makanae, Yuhei Kido, Kohei Sase, Kohei Yoshii, Naomi Fujita, Satoshi Physiol Rep Original Research Previous studies have reported that different modes of muscle contraction (i.e., eccentric or concentric contraction) with similar contraction times can affect muscle proteolytic responses. However, the effect of different contraction modes on muscle proteolytic response under the same force−time integral (FTI: contraction force × time) has not been investigated. The purpose of this study was to investigate the effect of different contraction modes, with the same FTI, on acute proteolytic signaling responses. Eleven‐week‐old male Sprague–Dawley rats were randomly assigned to eccentric (EC), concentric (CC), or isometric contraction (IC) groups. Different modes of muscle contraction were performed on the right gastrocnemius muscle using electrical stimulation, with the left muscle acting as a control. In order to apply an equivalent FTI, the number of stimulation sets was modified between the groups. Muscle samples were taken immediately and three hours after exercise. Phosphorylation of FoxO3a at Ser253 was significantly increased immediately after exercise compared to controls irrespective of contraction mode. The mRNA levels of the ubiquitin ligases, MuRF1, and MAFbx mRNA were unchanged by contraction mode or time. Phosphorylation of ULK1 at Ser317 (positive regulatory site) and Ser757 (negative regulatory site) was significantly increased compared to controls, immediately or 3 h after exercise, in all contraction modes. The autophagy markers (LC3B‐II/I ratio and p62 expression) were unchanged, regardless of contraction mode. These data suggest that differences in contraction mode during resistance exercise with a constant FTI, are not factors in regulating proteolytic signaling in the early phase of skeletal muscle contraction. John Wiley and Sons Inc. 2017-08-04 /pmc/articles/PMC5555890/ /pubmed/28778992 http://dx.doi.org/10.14814/phy2.13364 Text en © 2017 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
Ato, Satoru
Makanae, Yuhei
Kido, Kohei
Sase, Kohei
Yoshii, Naomi
Fujita, Satoshi
The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title_full The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title_fullStr The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title_full_unstemmed The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title_short The effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
title_sort effect of different acute muscle contraction regimens on the expression of muscle proteolytic signaling proteins and genes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555890/
https://www.ncbi.nlm.nih.gov/pubmed/28778992
http://dx.doi.org/10.14814/phy2.13364
work_keys_str_mv AT atosatoru theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT makanaeyuhei theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT kidokohei theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT sasekohei theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT yoshiinaomi theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT fujitasatoshi theeffectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT atosatoru effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT makanaeyuhei effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT kidokohei effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT sasekohei effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT yoshiinaomi effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes
AT fujitasatoshi effectofdifferentacutemusclecontractionregimensontheexpressionofmuscleproteolyticsignalingproteinsandgenes