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High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles

This study examined acute molecular responses to concurrent exercise involving different muscles. Eight men participated in a randomized crossover-trial with two sessions, one where they performed interval cycling followed by upper body resistance exercise (ER-Arm), and one with upper body resistanc...

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Autores principales: Moberg, Marcus, Apró, William, Cervenka, Igor, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Ruas, Jorge L., Blomstrand, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979871/
https://www.ncbi.nlm.nih.gov/pubmed/33742064
http://dx.doi.org/10.1038/s41598-021-85733-1
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author Moberg, Marcus
Apró, William
Cervenka, Igor
Ekblom, Björn
van Hall, Gerrit
Holmberg, Hans-Christer
Ruas, Jorge L.
Blomstrand, Eva
author_facet Moberg, Marcus
Apró, William
Cervenka, Igor
Ekblom, Björn
van Hall, Gerrit
Holmberg, Hans-Christer
Ruas, Jorge L.
Blomstrand, Eva
author_sort Moberg, Marcus
collection PubMed
description This study examined acute molecular responses to concurrent exercise involving different muscles. Eight men participated in a randomized crossover-trial with two sessions, one where they performed interval cycling followed by upper body resistance exercise (ER-Arm), and one with upper body resistance exercise only (R-Arm). Biopsies were taken from the triceps prior to and immediately, 90- and 180-min following exercise. Immediately after resistance exercise, the elevation in S6K1 activity was smaller and the 4E-BP1:eIF4E interaction greater in ER-Arm, but this acute attenuation disappeared during recovery. The protein synthetic rate in triceps was greater following exercise than at rest, with no difference between trials. The level of PGC-1α1 mRNA increased to greater extent in ER-Arm than R-Arm after 90 min of recovery, as was PGC-1α4 mRNA after both 90 and 180 min. Levels of MuRF-1 mRNA was unchanged in R-Arm, but elevated during recovery in ER-Arm, whereas MAFbx mRNA levels increased slightly in both trials. RNA sequencing in a subgroup of subjects revealed 862 differently expressed genes with ER-Arm versus R-Arm during recovery. These findings suggest that leg cycling prior to arm resistance exercise causes systemic changes that potentiate induction of specific genes in the triceps, without compromising the anabolic response.
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spelling pubmed-79798712021-03-25 High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles Moberg, Marcus Apró, William Cervenka, Igor Ekblom, Björn van Hall, Gerrit Holmberg, Hans-Christer Ruas, Jorge L. Blomstrand, Eva Sci Rep Article This study examined acute molecular responses to concurrent exercise involving different muscles. Eight men participated in a randomized crossover-trial with two sessions, one where they performed interval cycling followed by upper body resistance exercise (ER-Arm), and one with upper body resistance exercise only (R-Arm). Biopsies were taken from the triceps prior to and immediately, 90- and 180-min following exercise. Immediately after resistance exercise, the elevation in S6K1 activity was smaller and the 4E-BP1:eIF4E interaction greater in ER-Arm, but this acute attenuation disappeared during recovery. The protein synthetic rate in triceps was greater following exercise than at rest, with no difference between trials. The level of PGC-1α1 mRNA increased to greater extent in ER-Arm than R-Arm after 90 min of recovery, as was PGC-1α4 mRNA after both 90 and 180 min. Levels of MuRF-1 mRNA was unchanged in R-Arm, but elevated during recovery in ER-Arm, whereas MAFbx mRNA levels increased slightly in both trials. RNA sequencing in a subgroup of subjects revealed 862 differently expressed genes with ER-Arm versus R-Arm during recovery. These findings suggest that leg cycling prior to arm resistance exercise causes systemic changes that potentiate induction of specific genes in the triceps, without compromising the anabolic response. Nature Publishing Group UK 2021-03-19 /pmc/articles/PMC7979871/ /pubmed/33742064 http://dx.doi.org/10.1038/s41598-021-85733-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moberg, Marcus
Apró, William
Cervenka, Igor
Ekblom, Björn
van Hall, Gerrit
Holmberg, Hans-Christer
Ruas, Jorge L.
Blomstrand, Eva
High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title_full High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title_fullStr High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title_full_unstemmed High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title_short High-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
title_sort high-intensity leg cycling alters the molecular response to resistance exercise in the arm muscles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979871/
https://www.ncbi.nlm.nih.gov/pubmed/33742064
http://dx.doi.org/10.1038/s41598-021-85733-1
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