Department of Immunology, Key Laboratory of Cancer Prevention and Therapy, Tianjin Cancer Institute and Hospital, Tianjin Medical University, Tianjin, PR China.
J Pharm Pharmacol. 2010 Mar;62(3):332-8. doi: 10.1211/jpp.62.03.0007.
Toxicity caused by pharmacological and chemical substances, including carbon tetrachloride (CCl(4)), 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 CCl(4)-induced liver injury in mice.
Mice were treated with CCl(4) 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-alpha level, respectively.
CCl(4) 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 CCl(4)-induced disruption of liver function. Importantly, rBPTI reduced CCl(4)-induced liver oxidative stress response and pro-inflammatory cytokine production.
These results indicated that rBPTI exerted a protective effect on CCl(4)-induced liver injury in mice. Thus, rBPTI may have potential application for prevention of liver injury induced by metabolism of drugs and toxic substances.
药理学和化学物质(包括四氯化碳(CCl4))引起的毒性是肝损伤的主要病理因素。因此,需要预防毒性的策略来维持健康的肝脏。本研究旨在确定重组牛胰蛋白酶抑制剂(rBPTI),一种非特异性丝氨酸蛋白酶抑制剂,是否可以预防 CCl4 诱导的小鼠肝损伤。
在存在或不存在 rBPTI 共同处理的情况下,用 CCl4 处理小鼠。制备肝组织切片进行组织病理学评估。通过检测血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)以及肝指数来评估肝功能。通过检测肝丙二醛水平和谷胱甘肽及超氧化物歧化酶活性以及血清肿瘤坏死因子-α水平,分别检测肝氧化应激和炎症。
CCl4 诱导肝细胞坏死、炎症细胞浸润和脂肪变性,rBPTI 以浓度依赖的方式改善了这种情况。此外,rBPTI 防止了 CCl4 引起的肝功能障碍。重要的是,rBPTI 降低了 CCl4 诱导的肝氧化应激反应和促炎细胞因子的产生。
这些结果表明,rBPTI 对 CCl4 诱导的小鼠肝损伤具有保护作用。因此,rBPTI 可能具有预防药物和有毒物质代谢引起的肝损伤的应用潜力。