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Muscle-to-Brain Signaling Via Myokines and Myometabolites

Skeletal muscle health and function are important determinants of systemic metabolic homeostasis and organism-wide responses, including disease outcome. While it is well known that exercise protects the central nervous system (CNS) from aging and disease, only recently this has been found to depend...

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Detalles Bibliográficos
Autores principales: Rai, Mamta, Demontis, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661353/
https://www.ncbi.nlm.nih.gov/pubmed/36448045
http://dx.doi.org/10.3233/BPL-210133
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author Rai, Mamta
Demontis, Fabio
author_facet Rai, Mamta
Demontis, Fabio
author_sort Rai, Mamta
collection PubMed
description Skeletal muscle health and function are important determinants of systemic metabolic homeostasis and organism-wide responses, including disease outcome. While it is well known that exercise protects the central nervous system (CNS) from aging and disease, only recently this has been found to depend on the endocrine capacity of skeletal muscle. Here, we review muscle-secreted growth factors and cytokines (myokines), metabolites (myometabolites), and other unconventional signals (e.g. bioactive lipid species, enzymes, and exosomes) that mediate muscle-brain and muscle-retina communication and neuroprotection in response to exercise and associated processes, such as the muscle unfolded protein response and metabolic stress. In addition to impacting proteostasis, neurogenesis, and cognitive functions, muscle-brain signaling influences complex brain-dependent behaviors, such as depression, sleeping patterns, and biosynthesis of neurotransmitters. Moreover, myokine signaling adapts feeding behavior to meet the energy demands of skeletal muscle. Contrary to protective myokines induced by exercise and associated signaling pathways, inactivity and muscle wasting may derange myokine expression and secretion and in turn compromise CNS function. We propose that tailoring muscle-to-CNS signaling by modulating myokines and myometabolites may combat age-related neurodegeneration and brain diseases that are influenced by systemic signals.
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spelling pubmed-96613532022-11-28 Muscle-to-Brain Signaling Via Myokines and Myometabolites Rai, Mamta Demontis, Fabio Brain Plast Review Skeletal muscle health and function are important determinants of systemic metabolic homeostasis and organism-wide responses, including disease outcome. While it is well known that exercise protects the central nervous system (CNS) from aging and disease, only recently this has been found to depend on the endocrine capacity of skeletal muscle. Here, we review muscle-secreted growth factors and cytokines (myokines), metabolites (myometabolites), and other unconventional signals (e.g. bioactive lipid species, enzymes, and exosomes) that mediate muscle-brain and muscle-retina communication and neuroprotection in response to exercise and associated processes, such as the muscle unfolded protein response and metabolic stress. In addition to impacting proteostasis, neurogenesis, and cognitive functions, muscle-brain signaling influences complex brain-dependent behaviors, such as depression, sleeping patterns, and biosynthesis of neurotransmitters. Moreover, myokine signaling adapts feeding behavior to meet the energy demands of skeletal muscle. Contrary to protective myokines induced by exercise and associated signaling pathways, inactivity and muscle wasting may derange myokine expression and secretion and in turn compromise CNS function. We propose that tailoring muscle-to-CNS signaling by modulating myokines and myometabolites may combat age-related neurodegeneration and brain diseases that are influenced by systemic signals. IOS Press 2022-10-21 /pmc/articles/PMC9661353/ /pubmed/36448045 http://dx.doi.org/10.3233/BPL-210133 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Rai, Mamta
Demontis, Fabio
Muscle-to-Brain Signaling Via Myokines and Myometabolites
title Muscle-to-Brain Signaling Via Myokines and Myometabolites
title_full Muscle-to-Brain Signaling Via Myokines and Myometabolites
title_fullStr Muscle-to-Brain Signaling Via Myokines and Myometabolites
title_full_unstemmed Muscle-to-Brain Signaling Via Myokines and Myometabolites
title_short Muscle-to-Brain Signaling Via Myokines and Myometabolites
title_sort muscle-to-brain signaling via myokines and myometabolites
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661353/
https://www.ncbi.nlm.nih.gov/pubmed/36448045
http://dx.doi.org/10.3233/BPL-210133
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