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Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics
Although physical activity is a health-promoting, popular global pastime, regular engagement in strenuous exercises, such as long-distance endurance running races, has been associated with a variety of detrimental physiological and immunological health effects. The resulting altered physiological st...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541139/ https://www.ncbi.nlm.nih.gov/pubmed/34677371 http://dx.doi.org/10.3390/metabo11100656 |
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author | Bester, Rachelle Stander, Zinandré Mason, Shayne Keane, Karen M. Howatson, Glyn Clifford, Tom Stevenson, Emma J. Loots, Du Toit |
author_facet | Bester, Rachelle Stander, Zinandré Mason, Shayne Keane, Karen M. Howatson, Glyn Clifford, Tom Stevenson, Emma J. Loots, Du Toit |
author_sort | Bester, Rachelle |
collection | PubMed |
description | Although physical activity is a health-promoting, popular global pastime, regular engagement in strenuous exercises, such as long-distance endurance running races, has been associated with a variety of detrimental physiological and immunological health effects. The resulting altered physiological state has previously been associated with fluctuations in various key metabolite concentrations; however, limited literature exists pertaining to the global/holistic metabolic changes that are induced by such. This investigation subsequently aims at elucidating the metabolic changes induced by a marathon by employing an untargeted proton nuclear magnetic resonance ((1)H-NMR) spectrometry metabolomics approach. A principal component analysis (PCA) plot revealed a natural differentiation between pre- and post-marathon metabolic profiles of the 30-athlete cohort, where 17 metabolite fluctuations were deemed to be statistically significant. These included reduced concentrations of various amino acids (AA) along with elevated concentrations of ketone bodies, glycolysis, tricarboxylic acid (TCA) cycle, and AA catabolism intermediates. Moreover, elevated concentrations of creatinine and creatine in the post-marathon group supports previous findings of marathon-induced muscle damage. Collectively, the results of this investigation characterize the strenuous metabolic load induced by a marathon and the consequential regulation of main energy-producing pathways to accommodate this, and a better description of the cause of the physiological changes seen after the completion of a marathon. |
format | Online Article Text |
id | pubmed-8541139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85411392021-10-24 Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics Bester, Rachelle Stander, Zinandré Mason, Shayne Keane, Karen M. Howatson, Glyn Clifford, Tom Stevenson, Emma J. Loots, Du Toit Metabolites Article Although physical activity is a health-promoting, popular global pastime, regular engagement in strenuous exercises, such as long-distance endurance running races, has been associated with a variety of detrimental physiological and immunological health effects. The resulting altered physiological state has previously been associated with fluctuations in various key metabolite concentrations; however, limited literature exists pertaining to the global/holistic metabolic changes that are induced by such. This investigation subsequently aims at elucidating the metabolic changes induced by a marathon by employing an untargeted proton nuclear magnetic resonance ((1)H-NMR) spectrometry metabolomics approach. A principal component analysis (PCA) plot revealed a natural differentiation between pre- and post-marathon metabolic profiles of the 30-athlete cohort, where 17 metabolite fluctuations were deemed to be statistically significant. These included reduced concentrations of various amino acids (AA) along with elevated concentrations of ketone bodies, glycolysis, tricarboxylic acid (TCA) cycle, and AA catabolism intermediates. Moreover, elevated concentrations of creatinine and creatine in the post-marathon group supports previous findings of marathon-induced muscle damage. Collectively, the results of this investigation characterize the strenuous metabolic load induced by a marathon and the consequential regulation of main energy-producing pathways to accommodate this, and a better description of the cause of the physiological changes seen after the completion of a marathon. MDPI 2021-09-27 /pmc/articles/PMC8541139/ /pubmed/34677371 http://dx.doi.org/10.3390/metabo11100656 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bester, Rachelle Stander, Zinandré Mason, Shayne Keane, Karen M. Howatson, Glyn Clifford, Tom Stevenson, Emma J. Loots, Du Toit Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title | Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title_full | Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title_fullStr | Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title_full_unstemmed | Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title_short | Characterizing Marathon-Induced Metabolic Changes Using (1)H-NMR Metabolomics |
title_sort | characterizing marathon-induced metabolic changes using (1)h-nmr metabolomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541139/ https://www.ncbi.nlm.nih.gov/pubmed/34677371 http://dx.doi.org/10.3390/metabo11100656 |
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