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Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults

Regular exercise is associated with changes in peripheral blood mononuclear cell (PBMC) proportions that have enhanced effector functions in young and old adults; however, the effects of acute exercise on PBMC nutrient sensors and metabolic function in active young adults is unknown. To fill this ga...

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Autores principales: Theall, Bailey, Stampley, James, Cho, Eunhan, Granger, Joshua, Johannsen, Neil M., Irving, Brian A., Spielmann, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8661513/
https://www.ncbi.nlm.nih.gov/pubmed/34889067
http://dx.doi.org/10.14814/phy2.15147
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author Theall, Bailey
Stampley, James
Cho, Eunhan
Granger, Joshua
Johannsen, Neil M.
Irving, Brian A.
Spielmann, Guillaume
author_facet Theall, Bailey
Stampley, James
Cho, Eunhan
Granger, Joshua
Johannsen, Neil M.
Irving, Brian A.
Spielmann, Guillaume
author_sort Theall, Bailey
collection PubMed
description Regular exercise is associated with changes in peripheral blood mononuclear cell (PBMC) proportions that have enhanced effector functions in young and old adults; however, the effects of acute exercise on PBMC nutrient sensors and metabolic function in active young adults is unknown. To fill this gap, activation status and nutrient‐sensing mechanisms of PBMCs isolated from 21 healthy active adults (20–35 yr; 36.5 ± 6.3 V̇O(2peak)) were characterized before and after 30 min of moderate‐to‐vigorous cycling (65%–75% V̇O(2peak)). In addition, changes in PBMC mitochondrial respiratory function in response to exercise were assessed using high‐resolution respirometry. There was an increase in the number of activated CD69+/CD4 (79% increase) and CD69+/CD8 (166% increase) T‐cells in response to the acute bout of exercise, while the nutrient‐sensing mechanisms remained unchanged. PBMC mitochondrial respiration did not increase on a cell‐per‐cell basis, however, mitochondrial oxidative capacity (OXPHOS) increased at the tissue level (18.6 pmol/(s*ml blood) versus 29.3 pmol/(s*ml blood); p < 0.05) in response to acute exercise. Thus, this study shows that acute exercise preferentially mobilizes activated T‐cells while concomitantly increasing PBMC mitochondrial oxidative capacity at the tissue level, rather than acutely changing mitochondrial oxidative capacity at the cellular level in young adults.
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spelling pubmed-86615132021-12-21 Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults Theall, Bailey Stampley, James Cho, Eunhan Granger, Joshua Johannsen, Neil M. Irving, Brian A. Spielmann, Guillaume Physiol Rep Original Articles Regular exercise is associated with changes in peripheral blood mononuclear cell (PBMC) proportions that have enhanced effector functions in young and old adults; however, the effects of acute exercise on PBMC nutrient sensors and metabolic function in active young adults is unknown. To fill this gap, activation status and nutrient‐sensing mechanisms of PBMCs isolated from 21 healthy active adults (20–35 yr; 36.5 ± 6.3 V̇O(2peak)) were characterized before and after 30 min of moderate‐to‐vigorous cycling (65%–75% V̇O(2peak)). In addition, changes in PBMC mitochondrial respiratory function in response to exercise were assessed using high‐resolution respirometry. There was an increase in the number of activated CD69+/CD4 (79% increase) and CD69+/CD8 (166% increase) T‐cells in response to the acute bout of exercise, while the nutrient‐sensing mechanisms remained unchanged. PBMC mitochondrial respiration did not increase on a cell‐per‐cell basis, however, mitochondrial oxidative capacity (OXPHOS) increased at the tissue level (18.6 pmol/(s*ml blood) versus 29.3 pmol/(s*ml blood); p < 0.05) in response to acute exercise. Thus, this study shows that acute exercise preferentially mobilizes activated T‐cells while concomitantly increasing PBMC mitochondrial oxidative capacity at the tissue level, rather than acutely changing mitochondrial oxidative capacity at the cellular level in young adults. John Wiley and Sons Inc. 2021-12-10 /pmc/articles/PMC8661513/ /pubmed/34889067 http://dx.doi.org/10.14814/phy2.15147 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Theall, Bailey
Stampley, James
Cho, Eunhan
Granger, Joshua
Johannsen, Neil M.
Irving, Brian A.
Spielmann, Guillaume
Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title_full Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title_fullStr Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title_full_unstemmed Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title_short Impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
title_sort impact of acute exercise on peripheral blood mononuclear cells nutrient sensing and mitochondrial oxidative capacity in healthy young adults
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8661513/
https://www.ncbi.nlm.nih.gov/pubmed/34889067
http://dx.doi.org/10.14814/phy2.15147
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