Cargando…
Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide
Skeletal muscle is responsible for altered acute and chronic workload as induced by exercise. Skeletal muscle adaptations range from immediate change of contractility to structural adaptation to adjust the demanded performance capacities. These processes are regulated by mechanically and metabolical...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645679/ https://www.ncbi.nlm.nih.gov/pubmed/23538841 http://dx.doi.org/10.3390/ijms14047109 |
_version_ | 1782268521408888832 |
---|---|
author | Suhr, Frank Gehlert, Sebastian Grau, Marijke Bloch, Wilhelm |
author_facet | Suhr, Frank Gehlert, Sebastian Grau, Marijke Bloch, Wilhelm |
author_sort | Suhr, Frank |
collection | PubMed |
description | Skeletal muscle is responsible for altered acute and chronic workload as induced by exercise. Skeletal muscle adaptations range from immediate change of contractility to structural adaptation to adjust the demanded performance capacities. These processes are regulated by mechanically and metabolically induced signaling pathways, which are more or less involved in all of these regulations. Nitric oxide is one of the central signaling molecules involved in functional and structural adaption in different cell types. It is mainly produced by nitric oxide synthases (NOS) and by non-enzymatic pathways also in skeletal muscle. The relevance of a NOS-dependent NO signaling in skeletal muscle is underlined by the differential subcellular expression of NOS1, NOS2, and NOS3, and the alteration of NO production provoked by changes of workload. In skeletal muscle, a variety of highly relevant tasks to maintain skeletal muscle integrity and proper signaling mechanisms during adaptation processes towards mechanical and metabolic stimulations are taken over by NO signaling. The NO signaling can be mediated by cGMP-dependent and -independent signaling, such as S-nitrosylation-dependent modulation of effector molecules involved in contractile and metabolic adaptation to exercise. In this review, we describe the most recent findings of NO signaling in skeletal muscle with a special emphasis on exercise conditions. However, to gain a more detailed understanding of the complex role of NO signaling for functional adaptation of skeletal muscle (during exercise), additional sophisticated studies are needed to provide deeper insights into NO-mediated signaling and the role of non-enzymatic-derived NO in skeletal muscle physiology. |
format | Online Article Text |
id | pubmed-3645679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-36456792013-05-13 Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide Suhr, Frank Gehlert, Sebastian Grau, Marijke Bloch, Wilhelm Int J Mol Sci Review Skeletal muscle is responsible for altered acute and chronic workload as induced by exercise. Skeletal muscle adaptations range from immediate change of contractility to structural adaptation to adjust the demanded performance capacities. These processes are regulated by mechanically and metabolically induced signaling pathways, which are more or less involved in all of these regulations. Nitric oxide is one of the central signaling molecules involved in functional and structural adaption in different cell types. It is mainly produced by nitric oxide synthases (NOS) and by non-enzymatic pathways also in skeletal muscle. The relevance of a NOS-dependent NO signaling in skeletal muscle is underlined by the differential subcellular expression of NOS1, NOS2, and NOS3, and the alteration of NO production provoked by changes of workload. In skeletal muscle, a variety of highly relevant tasks to maintain skeletal muscle integrity and proper signaling mechanisms during adaptation processes towards mechanical and metabolic stimulations are taken over by NO signaling. The NO signaling can be mediated by cGMP-dependent and -independent signaling, such as S-nitrosylation-dependent modulation of effector molecules involved in contractile and metabolic adaptation to exercise. In this review, we describe the most recent findings of NO signaling in skeletal muscle with a special emphasis on exercise conditions. However, to gain a more detailed understanding of the complex role of NO signaling for functional adaptation of skeletal muscle (during exercise), additional sophisticated studies are needed to provide deeper insights into NO-mediated signaling and the role of non-enzymatic-derived NO in skeletal muscle physiology. Molecular Diversity Preservation International (MDPI) 2013-03-28 /pmc/articles/PMC3645679/ /pubmed/23538841 http://dx.doi.org/10.3390/ijms14047109 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Suhr, Frank Gehlert, Sebastian Grau, Marijke Bloch, Wilhelm Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title | Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title_full | Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title_fullStr | Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title_full_unstemmed | Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title_short | Skeletal Muscle Function during Exercise—Fine-Tuning of Diverse Subsystems by Nitric Oxide |
title_sort | skeletal muscle function during exercise—fine-tuning of diverse subsystems by nitric oxide |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645679/ https://www.ncbi.nlm.nih.gov/pubmed/23538841 http://dx.doi.org/10.3390/ijms14047109 |
work_keys_str_mv | AT suhrfrank skeletalmusclefunctionduringexercisefinetuningofdiversesubsystemsbynitricoxide AT gehlertsebastian skeletalmusclefunctionduringexercisefinetuningofdiversesubsystemsbynitricoxide AT graumarijke skeletalmusclefunctionduringexercisefinetuningofdiversesubsystemsbynitricoxide AT blochwilhelm skeletalmusclefunctionduringexercisefinetuningofdiversesubsystemsbynitricoxide |