Please use this identifier to cite or link to this item: https://doi.org/10.21203/rs.2.23593/v1
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dc.titleConcurrent high-intensity aerobic and resistance exercise modulates systemic release of alarmins (HMGB1, S100A8/A9, HSP70) and inflammatory biomarkers in healthy young men: a pilot study
dc.contributor.authorGoh, Jorming
dc.contributor.authorHofmann, Peter
dc.contributor.authorAw, Ning Hong
dc.contributor.authorTan, Poh Ling
dc.contributor.authorTschakert, Gerhard
dc.contributor.authorMueller, Alexander
dc.contributor.authorWong, Siew Cheng
dc.contributor.authorTan, Frankie
dc.contributor.authorGan, Linda Seo Hwee
dc.date.accessioned2022-04-21T08:46:20Z
dc.date.available2022-04-21T08:46:20Z
dc.date.issued2020-12
dc.identifier.citationGoh, Jorming, Hofmann, Peter, Aw, Ning Hong, Tan, Poh Ling, Tschakert, Gerhard, Mueller, Alexander, Wong, Siew Cheng, Tan, Frankie, Gan, Linda Seo Hwee (2020-12). Concurrent high-intensity aerobic and resistance exercise modulates systemic release of alarmins (HMGB1, S100A8/A9, HSP70) and inflammatory biomarkers in healthy young men: a pilot study. Translational Medicine Communications 5 (1). ScholarBank@NUS Repository. https://doi.org/10.21203/rs.2.23593/v1
dc.identifier.issn2396-832X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/219451
dc.description.abstract<jats:title>Abstract</jats:title> <jats:p><jats:bold>Background: </jats:bold>Intense exercise is a systemic stressor associated with the release of “danger” molecules – alarmins, by damaged or dying cells into systemic circulation to evoke a sterile inflammatory response. Compared with research in clinical diseases, physiological responses of alarmins to exercise and training are not well studied. Short-term responses to exercise and training using a panel of alarmins – HMGB1, S100A8/A9, HSP70 and sRAGE may reveal unique aspects of stress responses to strenuous exercise with important ramifications when prescribing exercise to generally healthy adults. <jats:bold>Methods: </jats:bold>A 3-week, high-intensity training program was performed by healthy young men (N = 7). Concurrent aerobic and resistance exercises were performed on 3 consecutive days each week. Blood and saliva were collected before (<jats:italic>Pre</jats:italic>), immediately after (<jats:italic>Post</jats:italic>), and 30 min (<jats:italic>30 min</jats:italic>) after exercise each week, and 24 h after the final exercise session in week 3 (<jats:italic>24 h</jats:italic>). <jats:bold>Results: </jats:bold>Plasma HMGB1, S100A8/A9 and HSP70 increased from <jats:italic>Pre</jats:italic> to <jats:italic>Post </jats:italic>(P < 0.05)<jats:italic>,</jats:italic> although at different timepoints during the study, and displayed different kinetics from IL-10, IL-8 and IFN-γ, suggesting unique mechanisms involved in modulating their release and clearance. CD14<jats:sup>+</jats:sup>CD16<jats:sup>-</jats:sup> monocytes increased from <jats:italic>Pre </jats:italic>to <jats:italic>Post </jats:italic>across 3 weeks; CD14<jats:sup>+</jats:sup>CD16<jats:sup>+</jats:sup> monocytes increased from <jats:italic>Pre </jats:italic>to <jats:italic>Post </jats:italic>in<jats:italic> </jats:italic>week 2 and 3 (P < 0.05).<jats:italic> </jats:italic>ΔHMGB1 and ΔHSP70 correlated positively with ΔMCP-1 during 3 weeks of training, while ΔHMGB1 correlated positively with CD14<jats:sup>+</jats:sup>CD16<jats:sup>- </jats:sup>monocytes, suggesting higher alarmin release after strenuous exercise may involve increase in circulating monocytes. <jats:bold>Conclusions: </jats:bold>Perturbations in systemic alarmins are novel biological signatures for assessing the inflammatory milieu of healthy adults during high-intensity exercise.</jats:p>
dc.publisherSpringer Science and Business Media LLC
dc.sourceElements
dc.subjectExercise
dc.subjectAlarmins
dc.subjectHMGB1
dc.subjectS100A8/A9
dc.subjectHSP70
dc.subjectsRAGE
dc.typeArticle
dc.date.updated2022-04-21T02:06:28Z
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.contributor.departmentPAEDIATRICS
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.21203/rs.2.23593/v1
dc.description.sourcetitleTranslational Medicine Communications
dc.description.volume5
dc.description.issue1
dc.published.statePublished
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