Cargando…

The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle

Mechanistic target of rapamycin complex 1 (mTORC1) plays a central role in muscle protein synthesis and repeated bouts of resistance exercise (RE) blunt mTORC1 activation. However, the changes in the proteolytic signaling when recurrent RE bouts attenuate mTORC1 activation are unclear. Using a RE mo...

Descripción completa

Detalles Bibliográficos
Autores principales: Kotani, Takaya, Takegaki, Junya, Tamura, Yuki, Kouzaki, Karina, Nakazato, Koichi, Ishii, Naokata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123562/
https://www.ncbi.nlm.nih.gov/pubmed/33991444
http://dx.doi.org/10.14814/phy2.14842
_version_ 1783692943497887744
author Kotani, Takaya
Takegaki, Junya
Tamura, Yuki
Kouzaki, Karina
Nakazato, Koichi
Ishii, Naokata
author_facet Kotani, Takaya
Takegaki, Junya
Tamura, Yuki
Kouzaki, Karina
Nakazato, Koichi
Ishii, Naokata
author_sort Kotani, Takaya
collection PubMed
description Mechanistic target of rapamycin complex 1 (mTORC1) plays a central role in muscle protein synthesis and repeated bouts of resistance exercise (RE) blunt mTORC1 activation. However, the changes in the proteolytic signaling when recurrent RE bouts attenuate mTORC1 activation are unclear. Using a RE model of electrically stimulated rat skeletal muscle, this study aimed to clarify the effect of repeated RE bouts on acute proteolytic signaling, particularly the calpain, autophagy‐lysosome, and ubiquitin‐proteasome pathway. p70S6K and rpS6 phosphorylation, indicators of mTORC1 activity, were attenuated by repeated RE bouts. Calpain 3 protein was decreased at 6 h post‐RE in all exercised groups regardless of the bout number. Microtubule‐associated protein 1 light chain 3 beta‐II, an indicator of autophagosome formation, was increased at 3 h and repeated RE bouts increased at 6 h, post‐RE. Ubiquitinated proteins were increased following RE, but these increases were independent of the number of RE bouts. These results suggest that the magnitude of autophagosome formation was increased following RE when mTORC1 activity was attenuated with repeated bouts of RE.
format Online
Article
Text
id pubmed-8123562
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-81235622021-05-21 The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle Kotani, Takaya Takegaki, Junya Tamura, Yuki Kouzaki, Karina Nakazato, Koichi Ishii, Naokata Physiol Rep Original Articles Mechanistic target of rapamycin complex 1 (mTORC1) plays a central role in muscle protein synthesis and repeated bouts of resistance exercise (RE) blunt mTORC1 activation. However, the changes in the proteolytic signaling when recurrent RE bouts attenuate mTORC1 activation are unclear. Using a RE model of electrically stimulated rat skeletal muscle, this study aimed to clarify the effect of repeated RE bouts on acute proteolytic signaling, particularly the calpain, autophagy‐lysosome, and ubiquitin‐proteasome pathway. p70S6K and rpS6 phosphorylation, indicators of mTORC1 activity, were attenuated by repeated RE bouts. Calpain 3 protein was decreased at 6 h post‐RE in all exercised groups regardless of the bout number. Microtubule‐associated protein 1 light chain 3 beta‐II, an indicator of autophagosome formation, was increased at 3 h and repeated RE bouts increased at 6 h, post‐RE. Ubiquitinated proteins were increased following RE, but these increases were independent of the number of RE bouts. These results suggest that the magnitude of autophagosome formation was increased following RE when mTORC1 activity was attenuated with repeated bouts of RE. John Wiley and Sons Inc. 2021-05-15 /pmc/articles/PMC8123562/ /pubmed/33991444 http://dx.doi.org/10.14814/phy2.14842 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles
Kotani, Takaya
Takegaki, Junya
Tamura, Yuki
Kouzaki, Karina
Nakazato, Koichi
Ishii, Naokata
The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title_full The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title_fullStr The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title_full_unstemmed The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title_short The effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
title_sort effect of repeated bouts of electrical stimulation‐induced muscle contractions on proteolytic signaling in rat skeletal muscle
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123562/
https://www.ncbi.nlm.nih.gov/pubmed/33991444
http://dx.doi.org/10.14814/phy2.14842
work_keys_str_mv AT kotanitakaya theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT takegakijunya theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT tamurayuki theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT kouzakikarina theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT nakazatokoichi theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT ishiinaokata theeffectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT kotanitakaya effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT takegakijunya effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT tamurayuki effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT kouzakikarina effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT nakazatokoichi effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle
AT ishiinaokata effectofrepeatedboutsofelectricalstimulationinducedmusclecontractionsonproteolyticsignalinginratskeletalmuscle