Recombinant bovine pancreatic trypsin inhibitor protects the liver from carbon tetrachloride-induced acute injury in mice

被引:5
作者
Yang, Lili [1 ]
Dong, Wen [2 ,3 ]
Yan, Fang [1 ,4 ]
Ren, Xiubao [1 ]
Hao, Xishan [1 ]
机构
[1] Tianjin Med Univ, Dept Immunol, Tianjin Canc Inst & Hosp, Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[2] Tianjin First Ctr Hosp, Dept Orthopaed, Tianjin, Peoples R China
[3] Tianjin Hongqiao Hosp, Dept Orthopaed Surg, Tianjin, Peoples R China
[4] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37212 USA
基金
国家高技术研究发展计划(863计划);
关键词
bovine pancreatic trypsin inhibitor; carbon tetrachloride; liver injury; SYSTEMIC INFLAMMATORY RESPONSE; TUMOR-NECROSIS-FACTOR; CARDIOPULMONARY BYPASS; APROTININ; HEPATOTOXICITY; EXPRESSION; REPAIR;
D O I
10.1211/jpp.62.03.0007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives Toxicity caused by pharmacological and chemical substances, including carbon tetrachloride (CCl4), is a major pathological factor for liver injury. Therefore, strategies to prevent toxicity are needed for maintaining a healthy liver. This study was designed to determine whether recombinant bovine pancreatic trypsin inhibitor (rBPTI), a non-specific serine protease inhibitor, prevents CCl4-induced liver injury in mice. Methods Mice were treated with CCl4 in the presence or absence of co-treatment with rBPTI. Liver sections were prepared for histopathological assessment. Liver function was evaluated by detecting serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and liver index. Liver oxidative stress and inflammation were examined by detecting the liver malondialdehyde level and glutathione and superoxide dismutase activity, and serum tumour necrosis factor-a level, respectively. Key findings CCl4 induced hepatocyte necrosis, inflammatory cell infiltration and fatty degeneration, which were ameliorated by co-treatment with rBPTI in a concentration-dependent manner. Furthermore, rBPTI prevented CCl4-induced disruption of liver function. Importantly, rBPTI reduced CCl4-induced liver oxidative stress response and proinflammatory cytokine production. Conclusions These results indicated that rBPTI exerted a protective effect on CCl4-induced liver injury in mice. Thus, rBPTI may have potential application for prevention of liver injury induced by metabolism of drugs and toxic substances.
引用
收藏
页码:332 / 338
页数:7
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