Resistive exercise blunts LPS-stimulated TNF α and Il-1β
Deutscher übersetzter Titel: | Widerstandstraining stumpft LPS stimuliertes TNF α und Il-1β ab |
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Autor: | Phillips, M.D.; Flynn, M.G.; McFarlin, B.K.; Stewart, L.K.; Timmerman, K.L. ; Ji, H. |
Erschienen in: | International journal of sports medicine |
Veröffentlicht: | 29 (2008), 2, S. 102-109, Lit. |
Format: | Literatur (SPOLIT) |
Publikationstyp: | Zeitschriftenartikel |
Medienart: | Gedruckte Ressource Elektronische Ressource (online) |
Sprache: | Englisch |
ISSN: | 0172-4622, 1439-3964 |
DOI: | 10.1055/s-2007-965115 |
Schlagworte: | |
Online Zugang: | |
Erfassungsnummer: | PU200808002370 |
Quelle: | BISp |
Abstract
To examine the influence of acute resistive exercise and “hormone status” on cytokine profile, 35 postmenopausal women (72 ± 6.2 yr) underwent a moderate-high-intensity resistive exercise bout or rested. There were 4 groups: no hormone replacement (NHR, n = 9), hormone replacement (HRT, n = 12), selective estrogen receptor modulator (SER, n = 7), or resting control (no hormone replacement, CON, n = 7). NHR, HRT, and SER exercised (3 sets, 10 exercises @ 80% 1RM). Blood was collected pre-exercise (PR), postexercise (PO), and two hours (2h) postexercise (same times for CON). Blood was diluted 1:10 in culture medium and incubated (37°C, 5% CO2, 24h) with lipopolysaccharide (LPS, 25 µg/ml). Serum and supernatant from LPS-stimulated blood were analyzed for IL-6, IL-1β, and TNF-α using ELISA. Resistive exercise increased PO serum IL-6, and PO LPS-stimulated IL-6 and IL-1β in the exercise groups (HRT, NHR, SER collapsed; EX, n = 28). LPS-stimulated IL-1β remained elevated at 2h in EX and was significantly higher than PR in CON at 2H. Expressed per monocyte, EX had significantly lower IL-1β and TNF-α LPS-stimulated production at PO and 2h compared to CON, indicating an exercise-induced blunting of an apparent diurnal response on cytokine production. In postmenopausal women, acute resistive exercise increased circulating IL-6, but reversed an apparent diurnal increase in LPS-stimulated IL-1β and TNF-α production with no influence of hormone replacement or raloxifene. Verf.-Referat