AAS ›› 2013, Vol. 44 ›› Issue (4 ): 550-553.doi: 10.3969/j.issn.0529-1356.2013.04.020

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Expression of peroxiredoxin I-thioredoxin, superoxide dismutases and catalases mRNA in hepatic ischemia-reperfusion injury of rats

ZHANG Li-hua1 WANG Qie2 LIU Zhao3 WANG Lei 2*   

  1. 1.The First Department of General Surgery, General Hospital of Northern China Oil Field,Hebei Renqiu 062552, China;2. Department of Anatomy, Hebei Medical University, Shijiazhuang 050017, China 3. Experimental Center, Clinic College, Hebei Medical University, Shijiazhuang 050031, China
  • Received:2012-06-21 Revised:2013-04-18 Online:2013-08-06 Published:2013-09-04

Abstract:

Objective To observe the expression change of peroxiredoxin I-thioredoxin (PrxI-Trx), superoxide dismutases (SOD) and catalases (CAT) in hepatic Ischemia-Reperfusion injury of rats, and to explore their role in oxidative-stress response.
Methods The hepatic ischemia-reperfusion injury model of rats was established by clipping the hepatic blood vessel released both hepatic left and middle lobes as well as bile duct pedicle with non-damage vascular clamp for 30 minutes. The serum and
hepatic tissues were taken 6 hours after clipping. The morphological changes were observed under a microscope using HE staining.The serum alanine aminotransferase(ALT) was detected by Automatic biochemical analyzer. The PrxI-Trx, SOD and CAT mRNA expression
were evaluated by RT-PCR. The protein level of PrxI, SOD and CAT were estimated by Western blotting. Results Compared with the control group, the ALT level and HE results of hepatic ischemia-reperfusion injury group showed that liver cells were significantly
impaired. The PrxI-Trx, CAT and SOD mRNA expression were increased significantly. The protein level of PrxI, SOD and CAT also increased significantly. Conclusion PrxI-Trx, SOD and CAT may play an important role in inhibiting the oxidative-stress response
induced by ischemia-reperfusion injury.

Key words: Ischemia-reperfusion injury, Peroxiredoxin I, Catalases, Superoxide dismutases, Oxidative stress, Western blotting, Rat