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首页> 外文期刊>The Journal of toxicological sciences >Changes in expression and production of heme oxygenase-1 in rats with acute liver injury induced by lipopolysaccharide
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Changes in expression and production of heme oxygenase-1 in rats with acute liver injury induced by lipopolysaccharide

机译:脂多糖诱导的急性肝损伤大鼠血红素加氧酶-1的表达和产生的变化

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To investigate the changes of heme oxygenase-1 (HO-1) expression and production in rats with acute liver injury induced by lipopolysaccharide (LPS), and explore the role of HO-1 in the pathogenesis of liver injury. Liver injury was assessed histologically and the serum level of alanine transaminase (ALT) and aspartate transaminase (AST) were examined. The activity of super oxide dismutase (SOD) and the content of malondialdehyde (MDA) and carbon monoxide (CO) in liver tissues were also examined at the same time. HO-1 mRNA expression was examined at different time points following LPS treatment and the expression of HO-1 protein was determined by immunohistochemical staining. Administration of LPS caused severe hepatic damage, characterized by significant elevation of serum ALT and AST levels and hepatic MDA content as well as a remarkable reduction of liver SOD activity at 24 hr as compared with those in the control group. HO-1 activity was elevated significantly after modeling, showing a time-dependent manner from 6 to 24 hr, while expression of HO-1 protein was increased remarkably from 6 to 24 hr. Endogenous CO concentration in the liver of control rats remained very low but was elevated significantly after LPS treatment (6, 12, 24 hr), which was in accordance with the changes of HO-1. HO-1 activity and protein are increased significantly in rats with acute liver injury induced by LPS, suggesting that HO-1 plays an important role in the pathogenesis of acute hepatic damage.
机译:目的探讨脂多糖(LPS)诱导的急性肝损伤大鼠血红素加氧酶-1(HO-1)表达和产生的变化,探讨HO-1在肝损伤发病机制中的作用。组织学评估肝损伤,并检查血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)的水平。同时检查肝脏组织中的超氧化物歧化酶(SOD)的活性以及丙二醛(MDA)和一氧化碳(CO)的含量。在LPS处理后的不同时间点检查HO-1 mRNA的表达,并通过免疫组织化学染色确定HO-1蛋白的表达。与对照组相比,LPS的给药引起严重的肝损害,其特征是血清ALT和AST水平和肝MDA含量显着升高,以及24小时肝脏SOD活性显着降低。建模后,HO-1活性显着提高,显示出时间依赖性,从6到24 hr,而HO-1蛋白的表达从6到24 hr显着增加。对照大鼠肝脏中的内源性CO浓度仍然很低,但是LPS处理后(6、12、24 hr)显着升高,这与HO-1的变化一致。在LPS诱导的急性肝损伤大鼠中,HO-1活性和蛋白质显着增加,表明HO-1在急性肝损伤的发病机理中起重要作用。

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