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Physical exercise associated with NO production: signaling pathways and significance in health and disease

Here we review available data on nitric oxide (NO)-mediated signaling in skeletal muscle during physical exercise. Nitric oxide modulates skeletal myocyte function, hormone regulation, and local microcirculation. Nitric oxide underlies the therapeutic effects of physical activity whereas the pharmac...

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Autores principales: Dyakova, Elena Y., Kapilevich, Leonid V., Shylko, Victor G., Popov, Sergey V., Anfinogenova, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382985/
https://www.ncbi.nlm.nih.gov/pubmed/25883934
http://dx.doi.org/10.3389/fcell.2015.00019
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author Dyakova, Elena Y.
Kapilevich, Leonid V.
Shylko, Victor G.
Popov, Sergey V.
Anfinogenova, Yana
author_facet Dyakova, Elena Y.
Kapilevich, Leonid V.
Shylko, Victor G.
Popov, Sergey V.
Anfinogenova, Yana
author_sort Dyakova, Elena Y.
collection PubMed
description Here we review available data on nitric oxide (NO)-mediated signaling in skeletal muscle during physical exercise. Nitric oxide modulates skeletal myocyte function, hormone regulation, and local microcirculation. Nitric oxide underlies the therapeutic effects of physical activity whereas the pharmacological modulators of NO-mediated signaling are the promising therapeutic agents in different diseases. Nitric oxide production increases in skeletal muscle in response to physical activity. This molecule can alter energy supply in skeletal muscle through hormonal modulation. Mitochondria in skeletal muscle tissue are highly abundant and play a pivotal role in metabolism. Considering NO a plausible regulator of mitochondrial biogenesis that directly affects cellular respiration, we discuss the mechanisms of NO-induced mitochondrial biogenesis in the skeletal muscle cells. We also review available data on myokines, the molecules that are expressed and released by the muscle fibers and exert autocrine, paracrine and/or endocrine effects. The article suggests the presence of putative interplay between NO-mediated signaling and myokines in skeletal muscle. Data demonstrate an important role of NO in various diseases and suggest that physical training may improve health of patients with diabetes, chronic heart failure, and even degenerative muscle diseases. We conclude that NO-associated signaling represents a promising target for the treatment of various diseases and for the achievement of better athletic performance.
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spelling pubmed-43829852015-04-16 Physical exercise associated with NO production: signaling pathways and significance in health and disease Dyakova, Elena Y. Kapilevich, Leonid V. Shylko, Victor G. Popov, Sergey V. Anfinogenova, Yana Front Cell Dev Biol Physiology Here we review available data on nitric oxide (NO)-mediated signaling in skeletal muscle during physical exercise. Nitric oxide modulates skeletal myocyte function, hormone regulation, and local microcirculation. Nitric oxide underlies the therapeutic effects of physical activity whereas the pharmacological modulators of NO-mediated signaling are the promising therapeutic agents in different diseases. Nitric oxide production increases in skeletal muscle in response to physical activity. This molecule can alter energy supply in skeletal muscle through hormonal modulation. Mitochondria in skeletal muscle tissue are highly abundant and play a pivotal role in metabolism. Considering NO a plausible regulator of mitochondrial biogenesis that directly affects cellular respiration, we discuss the mechanisms of NO-induced mitochondrial biogenesis in the skeletal muscle cells. We also review available data on myokines, the molecules that are expressed and released by the muscle fibers and exert autocrine, paracrine and/or endocrine effects. The article suggests the presence of putative interplay between NO-mediated signaling and myokines in skeletal muscle. Data demonstrate an important role of NO in various diseases and suggest that physical training may improve health of patients with diabetes, chronic heart failure, and even degenerative muscle diseases. We conclude that NO-associated signaling represents a promising target for the treatment of various diseases and for the achievement of better athletic performance. Frontiers Media S.A. 2015-04-02 /pmc/articles/PMC4382985/ /pubmed/25883934 http://dx.doi.org/10.3389/fcell.2015.00019 Text en Copyright © 2015 Dyakova, Kapilevich, Shylko, Popov and Anfinogenova. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Dyakova, Elena Y.
Kapilevich, Leonid V.
Shylko, Victor G.
Popov, Sergey V.
Anfinogenova, Yana
Physical exercise associated with NO production: signaling pathways and significance in health and disease
title Physical exercise associated with NO production: signaling pathways and significance in health and disease
title_full Physical exercise associated with NO production: signaling pathways and significance in health and disease
title_fullStr Physical exercise associated with NO production: signaling pathways and significance in health and disease
title_full_unstemmed Physical exercise associated with NO production: signaling pathways and significance in health and disease
title_short Physical exercise associated with NO production: signaling pathways and significance in health and disease
title_sort physical exercise associated with no production: signaling pathways and significance in health and disease
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382985/
https://www.ncbi.nlm.nih.gov/pubmed/25883934
http://dx.doi.org/10.3389/fcell.2015.00019
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