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World J Gastroenterol. Jan 28, 2008; 14(4): 590-594
Published online Jan 28, 2008. doi: 10.3748/wjg.14.590
Alleviation of ischemia/reperfusion injury in ob/ob mice by inhibiting UCP-2 expression in fatty liver
Chi-Dan Wan, Chun-You Wang, Tao Liu, Rui Cheng, Hong-Bo Wang
Chi-Dan Wan, Chun-You Wang, Tao Liu, Rui Cheng, Hong-Bo Wang, Department of General Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China
Correspondence to: Chi-Dan Wan, MD, Department of General Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China. chidanwan@163.com
Telephone: +86-27-85351623
Fax: +86-27-85351669
Received: April 4, 2007
Revised: September 10, 2007
Published online: January 28, 2008
Abstract

AIM: To investigate the protective effect of target suppression of uncoupling protein-2 (UCP-2) on ischemia/reperfusion (I/R) injury in fatty liver in ob/ob mice.

METHODS: Plasmids suppressing UCP-2 expression were constructed, and transfected into fatty liver cells cultured in vitro and the ob/ob mouse I/R injury model. Serum tumor necrosis factor (TNF)-α levels, UCP-2 mRNA expression, alanine aminotransferase (ALT) levels in ob/ob mice were tested, and the pathological changes in fatty liver were observed in experimental and control groups.

RESULTS: In ob/ob mouse I/R models, serum TNF-α levels were significantly higher than in normal controls. After the plasmids were transfected into the cultured cells and animal models, expression of UCP-2 mRNA was significantly reduced as compared with that in the control group (21.56 ± 0.15vs 2-0.45 ± 0.15, P < 0.05). In ob/ob mouse models, in which expression of UCP-2 was suppressed, serum ALT levels were significantly lower than those of other groups, and pathological analysis revealed that injury of liver tissues was significantly alleviated.

CONCLUSION: The target suppression of UCP-2 expression in fatty liver can alleviate the I/R injury in the ob/ob mice.

Keywords: ob/ob mice, Fatty liver, Uncoupling protein-2, Ischemia/reperfusion injury