The protective effect of heat shock protein 72 by Doxorubicin in cold ischemia-reperfusion injury of the rat liver.
- Author:
Hao CHEN
1
;
Cheng-hong PENG
;
Xia-xing DENG
;
Wei-hua QIU
;
Bai-yong SHEN
;
Wei-ping YANG
;
Hong-wei LI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Chemokines, CXC; biosynthesis; genetics; Cryopreservation; Doxorubicin; pharmacology; HSP72 Heat-Shock Proteins; biosynthesis; Liver; blood supply; drug effects; metabolism; Liver Transplantation; Male; RNA, Messenger; genetics; Random Allocation; Rats; Rats, Sprague-Dawley; Reperfusion Injury; etiology; prevention & control; Reverse Transcriptase Polymerase Chain Reaction; Tissue Survival; Tumor Necrosis Factor-alpha; biosynthesis; genetics
- From: Chinese Journal of Surgery 2006;44(5):310-313
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo observe induction of heat shock reaction by pretreatment of Doxorubicin (DXR) in long-term cold preservation-reperfusion injury of the rat liver.
METHODSThe rats were administered intravenously by DXR at a dose of 1 mg/kg body weight in DXR group and by saline in control group. After 48 hours, the rat liver was perfused by using cold University of Wisconsin (UW) solutions and was preserved in UW solution at 4 degrees C for 48 hours. Recipient liver was perfused for 1 and 3 hours after orthotopic liver transplantation. Tumor necrosis factor-alpha (TNF-alpha) mRNA, cytokine-induced neutrophil chemoattractant (CINC) mRNA, macrophage inflammatory protein (MIP-2) mRNA was measured by RT-PCR and heat shock protein 72 (HSP72), nuclear factor-kappaB (NF-kappaB) by Western blot. The serum levels of TNF-alpha, CINC, MIP-2 by ELISA and AST were measured. The survival rate of 7 days was observed.
RESULTSThe expression of TNF-alpha mRNA, CINC mRNA and MIP-2 mRNA was stronger in control group than in DXR group. HSP72 was expressed in SA group but not in control group and oppositely NF-kappaB was expressed in control group but not in DXR group. Serum AST, TNF-alpha, CINC and MIP-2 concentrations were significantly lower in DXR group than in control group (P < 0.05). The survival rate of 7 days was significantly higher in DXR group than in control group (50% vs. 0%, P < 0.05).
CONCLUSIONSThese data suggested that long-term cold ischemia-reperfusion injury was attenuated in liver graft with pretreatment of DXR. The induction of HSP72 may offer protection to hepatocytes by restraining the activation of NF-kappaB and inflammation.
