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ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run
The aim of the study was to reveal whether marathon running influences regulators of lipid metabolism i.e. angiopoietin-like protein 4 (ANGPTL4), interleukin 6 (IL-6) and tumor necrosis factor-α (TNF-α). Plasma concentration of ANGPTL4, IL-6, TNF-α and lipids were determined in samples collected fro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675781/ https://www.ncbi.nlm.nih.gov/pubmed/36402848 http://dx.doi.org/10.1038/s41598-022-17439-x |
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author | Górecka, Monika Krzemiński, Krzysztof Mikulski, Tomasz Ziemba, Andrzej Wojciech |
author_facet | Górecka, Monika Krzemiński, Krzysztof Mikulski, Tomasz Ziemba, Andrzej Wojciech |
author_sort | Górecka, Monika |
collection | PubMed |
description | The aim of the study was to reveal whether marathon running influences regulators of lipid metabolism i.e. angiopoietin-like protein 4 (ANGPTL4), interleukin 6 (IL-6) and tumor necrosis factor-α (TNF-α). Plasma concentration of ANGPTL4, IL-6, TNF-α and lipids were determined in samples collected from 11 male runners before the marathon, immediately after the run and at 90 min of recovery. Plasma ANGPTL4 increased during exercise from 55.5 ± 13.4 to 78.1 ± 15.0 ng/ml (P < 0.001). This was accompanied by a significant increase in IL-6, TNF-α, free fatty acids (FFA) and glycerol (Gly) and a decrease in triacylglycerols (TG). After 90 min of recovery ANGPTL4 and TG did not differ from the exercise values, while plasma IL-6, TNF-α, FFA and Gly concentration were significantly lower. The exercise-induced increase in plasma concentration of ANGPTL4 correlated positively with the rise in plasma IL-6, TNF-α, FFA and Gly and negatively with the duration of the run. The increase in plasma IL-6 and TNF-α correlated positively with the rise in Gly. Summarizing, marathon running induced an increase in plasma ANGPTL4 and the value was higher in faster runners. The increase in plasma FFA, IL-6 and TNF-α concentration during a marathon run may be involved in plasma ANGPTL4 release, which could be a compensatory mechanism against FFA-induced lipotoxicity and oxidative stress. All of the analyzed cytokines may stimulate lipolysis during exercise. |
format | Online Article Text |
id | pubmed-9675781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96757812022-11-21 ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run Górecka, Monika Krzemiński, Krzysztof Mikulski, Tomasz Ziemba, Andrzej Wojciech Sci Rep Article The aim of the study was to reveal whether marathon running influences regulators of lipid metabolism i.e. angiopoietin-like protein 4 (ANGPTL4), interleukin 6 (IL-6) and tumor necrosis factor-α (TNF-α). Plasma concentration of ANGPTL4, IL-6, TNF-α and lipids were determined in samples collected from 11 male runners before the marathon, immediately after the run and at 90 min of recovery. Plasma ANGPTL4 increased during exercise from 55.5 ± 13.4 to 78.1 ± 15.0 ng/ml (P < 0.001). This was accompanied by a significant increase in IL-6, TNF-α, free fatty acids (FFA) and glycerol (Gly) and a decrease in triacylglycerols (TG). After 90 min of recovery ANGPTL4 and TG did not differ from the exercise values, while plasma IL-6, TNF-α, FFA and Gly concentration were significantly lower. The exercise-induced increase in plasma concentration of ANGPTL4 correlated positively with the rise in plasma IL-6, TNF-α, FFA and Gly and negatively with the duration of the run. The increase in plasma IL-6 and TNF-α correlated positively with the rise in Gly. Summarizing, marathon running induced an increase in plasma ANGPTL4 and the value was higher in faster runners. The increase in plasma FFA, IL-6 and TNF-α concentration during a marathon run may be involved in plasma ANGPTL4 release, which could be a compensatory mechanism against FFA-induced lipotoxicity and oxidative stress. All of the analyzed cytokines may stimulate lipolysis during exercise. Nature Publishing Group UK 2022-11-19 /pmc/articles/PMC9675781/ /pubmed/36402848 http://dx.doi.org/10.1038/s41598-022-17439-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Górecka, Monika Krzemiński, Krzysztof Mikulski, Tomasz Ziemba, Andrzej Wojciech ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title | ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title_full | ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title_fullStr | ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title_full_unstemmed | ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title_short | ANGPTL4, IL-6 and TNF-α as regulators of lipid metabolism during a marathon run |
title_sort | angptl4, il-6 and tnf-α as regulators of lipid metabolism during a marathon run |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675781/ https://www.ncbi.nlm.nih.gov/pubmed/36402848 http://dx.doi.org/10.1038/s41598-022-17439-x |
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