Abstract
Resuscitated hemorrhagic shock is believed to promote the development of acute lung injury (ALI) by priming the immune system for an exaggerated inflammatory response to a second trivial stimulus. This work explored effects of TLR4 on hemorrhage-induced ALI and "second-hit" responses, and further explore the mechanisms involved in "second-hit" responses. Expression of HO-1, IL-10, lung W/D and MPO markedly increased at nearly all time-points examined in HSR/LPS group as compared with sham/LPS group in WT mice. In HSR/LPS mice, the induced amount of IL-10 and the expressions of HO-1 of WT mice were significantly higher compared with TLR-4d/d. This study provides in vivo evidence that pulmonary infections after LPS instillation contribute to local tissue release of pro-inflammatory mediators after HSR systemic. Activation of TLR4 might induce HO-1 expression and HO-1 modulates proinflammatory responses that are triggered via TLR4 signaling. © 2012 Springer Science+Business Media Dordrecht.
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Chen, C., Zhang, F., Zhang, Z., Peng, M., Wang, Y., & Chen, Y. (2013). TLR4 signaling-induced heme oxygenase upregulation in the acute lung injury: Role in hemorrhagic shock and two-hit induced lung inflammation. Molecular Biology Reports, 40(2), 1167–1172. https://doi.org/10.1007/s11033-012-2158-y
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