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High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men
This study investigated whether high-intensity exercise training alters the effect of N-acetylcysteine (a precursor of antioxidant glutathione) on exercise-related muscle ionic shifts. We assigned 20 recreationally-active men to 6 weeks of high-intensity exercise training, comprising three weekly se...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855150/ https://www.ncbi.nlm.nih.gov/pubmed/36670915 http://dx.doi.org/10.3390/antiox12010053 |
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author | Lemminger, Anders K. Fiorenza, Matteo Eibye, Kasper Bangsbo, Jens Hostrup, Morten |
author_facet | Lemminger, Anders K. Fiorenza, Matteo Eibye, Kasper Bangsbo, Jens Hostrup, Morten |
author_sort | Lemminger, Anders K. |
collection | PubMed |
description | This study investigated whether high-intensity exercise training alters the effect of N-acetylcysteine (a precursor of antioxidant glutathione) on exercise-related muscle ionic shifts. We assigned 20 recreationally-active men to 6 weeks of high-intensity exercise training, comprising three weekly sessions of 4–10 × 20-s all-out bouts interspersed by 2 min recovery (SET, n = 10), or habitual lifestyle maintenance (n = 10). Before and after SET, we measured ionic shifts across the working muscle, using leg arteriovenous balance technique, during one-legged knee-extensor exercise to exhaustion with and without N-acetylcysteine infusion. Furthermore, we sampled vastus lateralis muscle biopsies for analyses of metabolites, mitochondrial respiratory function, and proteins regulating ion transport and antioxidant defense. SET lowered exercise-related H(+), K(+), lactate(−), and Na(+) shifts and enhanced exercise performance by ≈45%. While N-acetylcysteine did not affect exercise-related ionic shifts before SET, it lowered H(+), HCO(3)(−), and Na(+) shifts after SET. SET enhanced muscle mitochondrial respiratory capacity and augmented the abundance of Na(+)/K(+)-ATPase subunits (α(1) and β(1)), ATP-sensitive K(+) channel subunit (Kir6.2), and monocarboxylate transporter-1, as well as superoxide dismutase-2 and glutathione peroxidase-1. Collectively, these findings demonstrate that high-intensity exercise training not only induces multiple adaptations that enhance the ability to counter exercise-related ionic shifts but also potentiates the effect of N-acetylcysteine on ionic shifts during exercise. |
format | Online Article Text |
id | pubmed-9855150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98551502023-01-21 High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men Lemminger, Anders K. Fiorenza, Matteo Eibye, Kasper Bangsbo, Jens Hostrup, Morten Antioxidants (Basel) Article This study investigated whether high-intensity exercise training alters the effect of N-acetylcysteine (a precursor of antioxidant glutathione) on exercise-related muscle ionic shifts. We assigned 20 recreationally-active men to 6 weeks of high-intensity exercise training, comprising three weekly sessions of 4–10 × 20-s all-out bouts interspersed by 2 min recovery (SET, n = 10), or habitual lifestyle maintenance (n = 10). Before and after SET, we measured ionic shifts across the working muscle, using leg arteriovenous balance technique, during one-legged knee-extensor exercise to exhaustion with and without N-acetylcysteine infusion. Furthermore, we sampled vastus lateralis muscle biopsies for analyses of metabolites, mitochondrial respiratory function, and proteins regulating ion transport and antioxidant defense. SET lowered exercise-related H(+), K(+), lactate(−), and Na(+) shifts and enhanced exercise performance by ≈45%. While N-acetylcysteine did not affect exercise-related ionic shifts before SET, it lowered H(+), HCO(3)(−), and Na(+) shifts after SET. SET enhanced muscle mitochondrial respiratory capacity and augmented the abundance of Na(+)/K(+)-ATPase subunits (α(1) and β(1)), ATP-sensitive K(+) channel subunit (Kir6.2), and monocarboxylate transporter-1, as well as superoxide dismutase-2 and glutathione peroxidase-1. Collectively, these findings demonstrate that high-intensity exercise training not only induces multiple adaptations that enhance the ability to counter exercise-related ionic shifts but also potentiates the effect of N-acetylcysteine on ionic shifts during exercise. MDPI 2022-12-27 /pmc/articles/PMC9855150/ /pubmed/36670915 http://dx.doi.org/10.3390/antiox12010053 Text en © 2022 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 Lemminger, Anders K. Fiorenza, Matteo Eibye, Kasper Bangsbo, Jens Hostrup, Morten High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title | High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title_full | High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title_fullStr | High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title_full_unstemmed | High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title_short | High-Intensity Exercise Training Alters the Effect of N-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men |
title_sort | high-intensity exercise training alters the effect of n-acetylcysteine on exercise-related muscle ionic shifts in men |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855150/ https://www.ncbi.nlm.nih.gov/pubmed/36670915 http://dx.doi.org/10.3390/antiox12010053 |
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