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Exercise-induced changes in stress hormones and cell adhesion molecules in obese men

PURPOSE: The current study examined the relationship between exercise-induced changes in stress hormones (epinephrine, norepinephrine, and cortisol) and vascular inflammatory markers (soluble intracellular adhesion molecule-1 [sICAM-1], soluble endothelial selectin [sE-selectin], and soluble vascula...

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Autores principales: Park, Jinkyung, Willoughby, Darryn S, Song, Joon Jin, Leutholtz, Brian C, Koh, Yunsuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836718/
https://www.ncbi.nlm.nih.gov/pubmed/29535548
http://dx.doi.org/10.2147/JIR.S158294
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author Park, Jinkyung
Willoughby, Darryn S
Song, Joon Jin
Leutholtz, Brian C
Koh, Yunsuk
author_facet Park, Jinkyung
Willoughby, Darryn S
Song, Joon Jin
Leutholtz, Brian C
Koh, Yunsuk
author_sort Park, Jinkyung
collection PubMed
description PURPOSE: The current study examined the relationship between exercise-induced changes in stress hormones (epinephrine, norepinephrine, and cortisol) and vascular inflammatory markers (soluble intracellular adhesion molecule-1 [sICAM-1], soluble endothelial selectin [sE-selectin], and soluble vascular adhesion molecule-1 [sVCAM-1]) in obese men over a 24-hour period following exercise at lower and higher intensity. PATIENTS AND METHODS: Fifteen physically inactive, obese, college-aged men performed a single bout of cycling exercise at lower and higher intensities (lower intensity: 50% of maximal heart rate, and higher intensity: 80% of maximal heart rate) in random order. Overnight fasting blood samples were collected at baseline, immediately postexercise (IPE), 1-hour PE (1-h PE), and 24-hour PE. Changes in stress hormones and inflammatory markers were analyzed with a repeated-measures analysis of variance using Bonferroni multiple comparisons and a linear regression analysis (p<0.05). RESULTS: sICAM-1, sVCAM-1, epinephrine, and norepinephrine did not change over time, while sE-selectin was significantly lower at 1-h PE (10.25±1.07 ng/mL, p=0.04) than at baseline (12.22±1.39 ng/mL). Cortisol and sICAM-1 were negatively related at 1-h PE following lower-intensity exercise (r(2)=0.34, p=0.02), whereas cortisol and sVCAM-1 were positively related at IPE following higher-intensity exercise (r(2)=0.36, p=0.02). CONCLUSION: Regardless of intensity, an acute bout of aerobic exercise may lower sE-selectin in sedentary obese men. Responses of cortisol are dependent on exercise intensity, and cortisol may be a key stress hormone playing a major role in regulating sICAM-1 and sVCAM-1.
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spelling pubmed-58367182018-03-13 Exercise-induced changes in stress hormones and cell adhesion molecules in obese men Park, Jinkyung Willoughby, Darryn S Song, Joon Jin Leutholtz, Brian C Koh, Yunsuk J Inflamm Res Original Research PURPOSE: The current study examined the relationship between exercise-induced changes in stress hormones (epinephrine, norepinephrine, and cortisol) and vascular inflammatory markers (soluble intracellular adhesion molecule-1 [sICAM-1], soluble endothelial selectin [sE-selectin], and soluble vascular adhesion molecule-1 [sVCAM-1]) in obese men over a 24-hour period following exercise at lower and higher intensity. PATIENTS AND METHODS: Fifteen physically inactive, obese, college-aged men performed a single bout of cycling exercise at lower and higher intensities (lower intensity: 50% of maximal heart rate, and higher intensity: 80% of maximal heart rate) in random order. Overnight fasting blood samples were collected at baseline, immediately postexercise (IPE), 1-hour PE (1-h PE), and 24-hour PE. Changes in stress hormones and inflammatory markers were analyzed with a repeated-measures analysis of variance using Bonferroni multiple comparisons and a linear regression analysis (p<0.05). RESULTS: sICAM-1, sVCAM-1, epinephrine, and norepinephrine did not change over time, while sE-selectin was significantly lower at 1-h PE (10.25±1.07 ng/mL, p=0.04) than at baseline (12.22±1.39 ng/mL). Cortisol and sICAM-1 were negatively related at 1-h PE following lower-intensity exercise (r(2)=0.34, p=0.02), whereas cortisol and sVCAM-1 were positively related at IPE following higher-intensity exercise (r(2)=0.36, p=0.02). CONCLUSION: Regardless of intensity, an acute bout of aerobic exercise may lower sE-selectin in sedentary obese men. Responses of cortisol are dependent on exercise intensity, and cortisol may be a key stress hormone playing a major role in regulating sICAM-1 and sVCAM-1. Dove Medical Press 2018-03-01 /pmc/articles/PMC5836718/ /pubmed/29535548 http://dx.doi.org/10.2147/JIR.S158294 Text en © 2018 Park et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Park, Jinkyung
Willoughby, Darryn S
Song, Joon Jin
Leutholtz, Brian C
Koh, Yunsuk
Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title_full Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title_fullStr Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title_full_unstemmed Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title_short Exercise-induced changes in stress hormones and cell adhesion molecules in obese men
title_sort exercise-induced changes in stress hormones and cell adhesion molecules in obese men
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836718/
https://www.ncbi.nlm.nih.gov/pubmed/29535548
http://dx.doi.org/10.2147/JIR.S158294
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