Brief Reports
Copyright ©2005 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 28, 2005; 11(12): 1825-1828
Published online Mar 28, 2005. doi: 10.3748/wjg.v11.i12.1825
Modulation of liver oxidant-antioxidant system by ischemic preconditioning during ischemia/reperfusion injury in rats
Guang-Jin Yuan, Jin-Chun Ma, Zuo-Jiong Gong, Xiao-Mei Sun, Shi-Hua Zheng, Xi Li
Guang-Jin Yuan, Zuo-Jiong Gong, Xiao-Mei Sun, Shi-Hua Zheng, Xi Li, Department of Infectious Diseases, Renmin Hospital of Wuhan University; National Key Laboratory of Virology Wuhan University, Ministry of Education, Medical School of Wuhan University, Wuhan 430060, Hubei Province, China
Jin-Chun Ma, Department of Infectious Diseases, Huangshi Ai Kang Hospital, Huangshi 435000, Hubei Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Zuo-Jiong Gong, Department of Infectious Diseases, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei Province, China. zjgong@163.com
Telephone: +86-27-88041919-8385 Fax: +86-27-88042292
Received: September 2, 2004
Revised: September 3, 2004
Accepted: October 26, 2004
Published online: March 28, 2005
Abstract

AIM: To investigate effects of ischemic pre-conditioning on the liver endogenous oxidant-antioxidant system during ischemia/reperfusion injury.

METHODS: Twenty-four male Sprague-Dawley rats were randomly divided into sham-operated (Sham), ischemia/reperfusion (I/R), ischemic pre-conditioning plus ischemia/reperfusion (IPC) groups. Serum ALT, AST and hyaluronic acid levels were assayed and pathologic alterations observed. Liver malondialdehyde (MDA) contents, endogenous antioxidant enzymes, superoxidase dismutase (SOD), catalase (CAT), gultathionine peroxidase (GSH-Px) activities, neutrophils accumulation marker, myeloperoxidase (MPO) activities were measured respectively.

RESULTS: Compared with I/R group, sinusoidal endothelial cells as well as hepatocytes damages, as assessed biochemically and histochemically, were improved significantly in IPC group; neutrophils infiltration was also markedly reduced. In IPC group, liver peroxidation, as measured by MDA contents, was significantly decreased when compared with I/R group; endogenous antioxidant enzymes, SOD, CAT and GSH-Px activities were markedly higher than that in I/R group.

CONCLUSION: Ischemic pre-conditioning exerts protective effects on both hepatic sinusoidal endothelial cells and hepatocytes during liver I/R injury. Its mechanisms may involve dimunition of neutrophils infiltration and modulation of the imbalance of endogenous oxidant-antioxidant system in the organism.

Keywords: Ischemic preconditioning; Ischemia/reperfusion; Antioxidant enzymes; Sinusoidal endothelial cells; Liver