Resistive Exercise Blunts LPS-stimulated TNF-α and Il-α.

Autor: Phillips, M. D., Flynn, M. G., McFarlin, B. K., Stewart, L. K., Timmerman, K. L., Ji, H.
Předmět:
Zdroj: International Journal of Sports Medicine; Feb2008, Vol. 29 Issue 2, p102-109, 8p, 1 Chart, 1 Graph
Abstrakt: 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) post-exercise (same times for CON). Blood was diluted 1:10 in culture medium and incubated (37°C, 5% CO2, 24 h) with lipopolysaccharide (LPS, 25 μg·ml-1). Serum and supernatant from LPS-stimulated blood were analyzed for lL-6, lL-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. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index