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Inflammation and Edema in the Lung and Kidney of Hemorrhagic Shock Rats Are Alleviated by Biliary Tract External Drainage Via the Heme Oxygenase-1 Pathway

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Journal Inflammation
Date 2015 Aug 9
PMID 26253294
Citations 3
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Abstract

The lung and kidney are two organs that are easily affected by hemorrhagic shock (HS). We investigated roles of biliary tract external drainage (BTED) in inflammation and edema of the lung and kidney in HS and its relationship with the heme oxygenase-1 (HO-1) pathway. Rat models of HS were induced by drawing blood from the femoral artery until a mean arterial pressure (MAP) of 40 ± 5 mmHg was achieved. A MAP of 40 ± 5 mmHg was maintained for 60 min. Thirty-six Sprague-Dawley rats were randomized to the following groups: sham group; HS group; HS + zinc protoporphyrin IX (ZnPP), a specific HO-1 inhibitor, group; HS + BTED group; HS + BTED + ZnPP group; and HS + BTED + bile infusion (BI) group. HO-1 levels, aquaporin-1 levels, and ratios of dry/wet in the lung and kidney increased markedly after BTED, but tumor necrosis factor-α and myeloperoxidase levels in the lung and kidney decreased significantly after BTED under HS conditions. Under the condition that HO-1 was inhibited by ZnPP, all these effects induced by BTED disappeared in the lung and kidney. These results demonstrated that inflammation and edema of the lung and kidney of HS rats are alleviated by BTED via the HO-1 pathway.

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References
1.
Le Tulzo Y, Shenkar R, Kaneko D, Moine P, Fantuzzi G, Dinarello C . Hemorrhage increases cytokine expression in lung mononuclear cells in mice: involvement of catecholamines in nuclear factor-kappaB regulation and cytokine expression. J Clin Invest. 1997; 99(7):1516-24. PMC: 507971. DOI: 10.1172/JCI119314. View

2.
Verkman A . Dissecting the roles of aquaporins in renal pathophysiology using transgenic mice. Semin Nephrol. 2008; 28(3):217-26. PMC: 2692584. DOI: 10.1016/j.semnephrol.2008.03.004. View

3.
Zhao W, Hu W . [A study of the role of heme oxygenase-1 expression in ventilator induced lung injury and its mechanism in rats]. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2010; 22(7):410-3. View

4.
Dey S, Sayers C, Verginadis I, Lehman S, Cheng Y, Cerniglia G . ATF4-dependent induction of heme oxygenase 1 prevents anoikis and promotes metastasis. J Clin Invest. 2015; 125(7):2592-608. PMC: 4563676. DOI: 10.1172/JCI78031. View

5.
Mai J, Qiu Q, Lin Y, Luo N, Zhang H, Wen Z . Angiotensin II-derived reactive oxygen species promote angiogenesis in human late endothelial progenitor cells through heme oxygenase-1 via ERK1/2 and AKT/PI3K pathways. Inflammation. 2014; 37(3):858-70. DOI: 10.1007/s10753-013-9806-9. View