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  4. Transient limb ischemia induces remote preconditioning in liver among rats: The protective role of heme oxygenase-1
 
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Transient limb ischemia induces remote preconditioning in liver among rats: The protective role of heme oxygenase-1

Journal
Transplantation
Journal Volume
81
Journal Issue
9
Pages
1311-1317
Date Issued
2006
Author(s)
I-RUE LAI  
KING-JEN CHANG  
Chen C.-F.
Tsai H.-W.
DOI
10.1097/01.tp.0000203555.14546.63
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-33744502373&doi=10.1097%2f01.tp.0000203555.14546.63&partnerID=40&md5=65844c79dda598ad73982d2ff722b55d
https://scholars.lib.ntu.edu.tw/handle/123456789/616749
Abstract
BACKGROUND: We have reported the protective role of heme oxygenase-1 (HO-1) in the mechanism of hypoxic preconditioning. We wish to investigate the role of HO-1 in remote preconditioning (RP) against hepatic ischemia/reperfusion (I/R) injury in rats. METHODS: The remote preconditioning was produced by four cycles of 10-min ischemia-reperfusion of the hind limb of rats. Partial hepatic ischemia was produced in the left lobes for 45 min followed by 240 min of reperfusion. Zinc-protoporphyrin IX (ZnPP), a specific inhibitor of HO enzymatic activity, was intra-peritoneally injected 1 hr before the ischemia-reperfusion injury in separate groups of RP rats. Serum alanine transaminase (ALT) levels, expression of hepatic HO-1 protein and mRNA, immunohistochemical staining and HO enzymatic activity were measured. RESULTS: HO-1 was induced in the livers of rats 4 hr after the RP stimuli, and the overexpression persisted for 24 hr. Immunohistochemical staining demonstrated induction of HO-1 in the hepatocytes. The peripheral lymphocytes did not express HO-1 after RP. RP diminished the elevation of serum ALT levels 4 hr after I/R injury (283.7+/-167.4 U L) when compared with controls (1297.7+/-729.3 U L) and RP+ ZnPP pretreated groups (1429.9+/-750.9 U L). The heme oxygenase activity in treated rats also correlated these results (286.8+/-34.3 pmol mg protein hr for the RP group, 156.3+/-27.5 pmol mg protein hr for the RP+ ZnPP pretreated group, and 170.6+/-19.4 pmol mg protein hr for the control group, 144.8+/-7.8 pmol mg protein hr for the control+ ZnPP pretreated group). CONCLUSION: Our results indicated that the induction of HO-1 in remote preconditioning played a protective role against hepatic I/R injury.
Type
journal article

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