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The acute effects of walking exercise intensity on systemic cytokines and oxidative stress

PURPOSE: Oxidative stress is associated with tissue cytokine secretion although the precise mechanism(s) underpinning this relationship during high intensity intermittent exercise remains unclear. This study investigates the acute response to a bout of high intensity intermittent walking (HIIW), com...

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Autores principales: Brown, Malcolm, McClean, Conor M., Davison, Gareth W., Brown, John C. W., Murphy, Marie H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153601/
https://www.ncbi.nlm.nih.gov/pubmed/30008038
http://dx.doi.org/10.1007/s00421-018-3930-z
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author Brown, Malcolm
McClean, Conor M.
Davison, Gareth W.
Brown, John C. W.
Murphy, Marie H.
author_facet Brown, Malcolm
McClean, Conor M.
Davison, Gareth W.
Brown, John C. W.
Murphy, Marie H.
author_sort Brown, Malcolm
collection PubMed
description PURPOSE: Oxidative stress is associated with tissue cytokine secretion although the precise mechanism(s) underpinning this relationship during high intensity intermittent exercise remains unclear. This study investigates the acute response to a bout of high intensity intermittent walking (HIIW), compared to continuous moderate intensity walking (CMW), on various cytokines and biomarkers of oxidative stress. METHODS: Seventeen (n = 17) apparently healthy male participants (aged 22.6 ± 4.6 years; [Formula: see text] : 53.7 ± 7.1 ml kg(−1) min(−1)) undertook a randomised crossover study consisting of two exercise trials: (1) HIIW requiring 3 × 5 min bursts at 80% [Formula: see text] (each separated by 5 min of walking at 30% [Formula: see text] ) and (2) CMW (60% [Formula: see text] for 30 min). Each trial was separated by 7 days. Venous blood samples were obtained pre-exercise, post-exercise and at 2, 4, 24 and 48 h post-exercise for determination of systemic inflammation (IL-6 and TNF-α), lipid soluble antioxidants and oxidative stress (LOOH, H(2)O(2) and the ascorbyl free radical). RESULTS: Both IL-6 and TNF-α increased immediately post exercise, regardless of intensity and remained elevated until at least 4 h (main effect for time; p < 0.05). While there was no change in either lipid peroxidation or free radical metabolism (Asc· and H(2)O(2)), α-tocopherol increased (pooled HIIW and CMW, p < 0.05), whereas lycopene decreased at 2 h post HIIW (p < 0.05). CONCLUSION: Bouts of both HIIW and CMW promote cytokine secretion post exercise, and this seems to be independent of oxidative stress. Further investigation is required to assess how such changes may underpin some of the transient health benefits of exercise.
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spelling pubmed-61536012018-10-04 The acute effects of walking exercise intensity on systemic cytokines and oxidative stress Brown, Malcolm McClean, Conor M. Davison, Gareth W. Brown, John C. W. Murphy, Marie H. Eur J Appl Physiol Original Article PURPOSE: Oxidative stress is associated with tissue cytokine secretion although the precise mechanism(s) underpinning this relationship during high intensity intermittent exercise remains unclear. This study investigates the acute response to a bout of high intensity intermittent walking (HIIW), compared to continuous moderate intensity walking (CMW), on various cytokines and biomarkers of oxidative stress. METHODS: Seventeen (n = 17) apparently healthy male participants (aged 22.6 ± 4.6 years; [Formula: see text] : 53.7 ± 7.1 ml kg(−1) min(−1)) undertook a randomised crossover study consisting of two exercise trials: (1) HIIW requiring 3 × 5 min bursts at 80% [Formula: see text] (each separated by 5 min of walking at 30% [Formula: see text] ) and (2) CMW (60% [Formula: see text] for 30 min). Each trial was separated by 7 days. Venous blood samples were obtained pre-exercise, post-exercise and at 2, 4, 24 and 48 h post-exercise for determination of systemic inflammation (IL-6 and TNF-α), lipid soluble antioxidants and oxidative stress (LOOH, H(2)O(2) and the ascorbyl free radical). RESULTS: Both IL-6 and TNF-α increased immediately post exercise, regardless of intensity and remained elevated until at least 4 h (main effect for time; p < 0.05). While there was no change in either lipid peroxidation or free radical metabolism (Asc· and H(2)O(2)), α-tocopherol increased (pooled HIIW and CMW, p < 0.05), whereas lycopene decreased at 2 h post HIIW (p < 0.05). CONCLUSION: Bouts of both HIIW and CMW promote cytokine secretion post exercise, and this seems to be independent of oxidative stress. Further investigation is required to assess how such changes may underpin some of the transient health benefits of exercise. Springer Berlin Heidelberg 2018-07-14 2018 /pmc/articles/PMC6153601/ /pubmed/30008038 http://dx.doi.org/10.1007/s00421-018-3930-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Brown, Malcolm
McClean, Conor M.
Davison, Gareth W.
Brown, John C. W.
Murphy, Marie H.
The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title_full The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title_fullStr The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title_full_unstemmed The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title_short The acute effects of walking exercise intensity on systemic cytokines and oxidative stress
title_sort acute effects of walking exercise intensity on systemic cytokines and oxidative stress
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153601/
https://www.ncbi.nlm.nih.gov/pubmed/30008038
http://dx.doi.org/10.1007/s00421-018-3930-z
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