Combination of hyperthermia and LPS may advance and augment systemic inflammatory response syndrome in rats
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Combination of hyperthermia and LPS may advance and augment systemic inflammatory response syndrome in rats
Journal of Army Medical UniversityVol. 29, Issue 6, Pages: 479-481(2007)
作者机构:
1. 南方医科大学:珠江医院心血管内科, 护理学院
2. 济南军区总医院脊髓修复科
作者简介:
基金信息:
DOI:
CLC:R363.123;R593.02;R392.11
Published:2007,
Published Online:30 March 2007,
稿件说明:
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LI ZHI-LIANG, ZHAO TING-BAO, LIU HONG-HUA. Combination of hyperthermia and LPS may advance and augment systemic inflammatory response syndrome in rats. [J]. Journal of army medical university, 2007, 29(6): 479-481.
DOI:
LI ZHI-LIANG, ZHAO TING-BAO, LIU HONG-HUA. Combination of hyperthermia and LPS may advance and augment systemic inflammatory response syndrome in rats. [J]. Journal of army medical university, 2007, 29(6): 479-481.DOI:
Combination of hyperthermia and LPS may advance and augment systemic inflammatory response syndrome in rats
Objective To investigate the effects of co-exposure to LPS and heat on plasma tumor necrosis factor-α (TNF-α)
interleukin-6 (IL-6)
malondialdehyde (MDA) and activity of superoxide dismutase (SOD) in rats. Methods Male pathogen-free Wistar rats were randomly assigned to the following groups: saline-injected normothermic control (Group C)
saline-injected heat exposure (Group H)
LPS-injected normothermic control (Group L)
LPS-injected heat exposure (Group HL). Mean arterial pressure (MAP) was continually monitored. Plasma levels of TNF-α
IL-6
MDA and SOD were determined at 0
40
80
120 min. Results The rats in Group HL displayed much lower MAP
higher MDA and lower SOD than the other 3 groups. The rats in Group HL displayed an early rise in plasma TNF-α
IL-6 at 40 min
the peak values of both at 80 min significantly higher than the other three groups at the same time piont. Conclusion Co-exposure to LPS and heat primes the rats to advance and augment systemic inflammatory response syndrome.