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Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus
Skeletal muscle undergoes metabolic remodelling in response to environmental hypoxia, yet aspects of this process remain controversial. Broadly, environmental hypoxia has been suggested to induce: (i) a loss of mitochondrial density; (ii) a substrate switch away from fatty acids and towards other su...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253994/ https://www.ncbi.nlm.nih.gov/pubmed/25473486 http://dx.doi.org/10.1186/2046-7648-3-19 |
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author | Horscroft, James A Murray, Andrew J |
author_facet | Horscroft, James A Murray, Andrew J |
author_sort | Horscroft, James A |
collection | PubMed |
description | Skeletal muscle undergoes metabolic remodelling in response to environmental hypoxia, yet aspects of this process remain controversial. Broadly, environmental hypoxia has been suggested to induce: (i) a loss of mitochondrial density; (ii) a substrate switch away from fatty acids and towards other substrates such as glucose, amino acids and ketone bodies; and (iii) a shift from aerobic to anaerobic metabolism. There remains a lack of a consensus in these areas, most likely as a consequence of the variations in degree and duration of hypoxic exposure, as well as the broad range of experimental parameters used as markers of metabolic processes. To attempt to resolve some of the controversies, we performed a comprehensive review of the literature pertaining to hypoxia-induced changes in skeletal muscle energy metabolism. We found evidence that mass-specific mitochondrial function is decreased prior to mass-specific mitochondrial density, implicating intra-mitochondrial changes in the response to environmental hypoxia. This loss of oxidative capacity does not appear to be matched by a loss of glycolytic capacity, which on the whole is not altered by environmental hypoxia. Environmental hypoxia does however induce a selective attenuation of fatty acid oxidation, whilst glucose uptake is maintained or increased, perhaps to support glycolysis in the face of a downregulation of oxidative metabolism, optimising the pathways of ATP synthesis for the hypoxic environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2046-7648-3-19) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4253994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42539942014-12-04 Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus Horscroft, James A Murray, Andrew J Extrem Physiol Med Review Skeletal muscle undergoes metabolic remodelling in response to environmental hypoxia, yet aspects of this process remain controversial. Broadly, environmental hypoxia has been suggested to induce: (i) a loss of mitochondrial density; (ii) a substrate switch away from fatty acids and towards other substrates such as glucose, amino acids and ketone bodies; and (iii) a shift from aerobic to anaerobic metabolism. There remains a lack of a consensus in these areas, most likely as a consequence of the variations in degree and duration of hypoxic exposure, as well as the broad range of experimental parameters used as markers of metabolic processes. To attempt to resolve some of the controversies, we performed a comprehensive review of the literature pertaining to hypoxia-induced changes in skeletal muscle energy metabolism. We found evidence that mass-specific mitochondrial function is decreased prior to mass-specific mitochondrial density, implicating intra-mitochondrial changes in the response to environmental hypoxia. This loss of oxidative capacity does not appear to be matched by a loss of glycolytic capacity, which on the whole is not altered by environmental hypoxia. Environmental hypoxia does however induce a selective attenuation of fatty acid oxidation, whilst glucose uptake is maintained or increased, perhaps to support glycolysis in the face of a downregulation of oxidative metabolism, optimising the pathways of ATP synthesis for the hypoxic environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2046-7648-3-19) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-28 /pmc/articles/PMC4253994/ /pubmed/25473486 http://dx.doi.org/10.1186/2046-7648-3-19 Text en © Horscroft and Murray; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Horscroft, James A Murray, Andrew J Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title | Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title_full | Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title_fullStr | Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title_full_unstemmed | Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title_short | Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
title_sort | skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253994/ https://www.ncbi.nlm.nih.gov/pubmed/25473486 http://dx.doi.org/10.1186/2046-7648-3-19 |
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