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EGCG对酒精性肝病小鼠肝脏铁调素表达影响

Effects of epigallocatechin-3-gallate on expression of hepcidin mRNA in liver of mice with alcoholic liver disease

  • 摘要: 目的 探讨表没食子儿茶素没食子酸酯(EGCG)对酒精性肝病(ALD)小鼠肝脏铁调素(hepcidin)mRNA表达影响。方法 6~8周龄雄性SPF级C57/BL6 小鼠随机分为对照组和造模组,造模组小鼠每日给予乙醇灌胃,并于造模第9 周随机分为模型组,EGCG 10、20、30 mg/kg组,4 周后处死小鼠,观察各组小鼠肝脏病理变化,测定谷丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)水平、肝脏铁含量,采用real-time PCR方法检测肝组织铁调素 mRNA表达。结果 与对照组比较,模型组小鼠血清ALT、AST分别为(237.25±50.26)、(442.38±56.31)U/L水平升高(P<0.01);肝脏病理观察显示,肝细胞呈中度脂肪变性;肝组织铁含量显著升高,肝脏铁调素 mRNA表达0.008±0.002明显降低(P<0.01);与模型组比较,EGCG 组小鼠血清ALT、AST水平分别为(53.75±6.67)、(151.75±13.81)U/L明显下降(P<0.01);肝铁含量及肝脏hepcidin mRNA0.051±0.011表达显著升高(P<0.01)。结论 结论EGCG 可以上调ALD 小鼠肝脏铁调素 mRNA表达,抑制小肠铁吸收,对酒精性肝病具有一定保护作用。 关键词没食子儿茶素没食子酸酯(EGCG);酒精性肝病(ALD);铁过载;铁调素(hepcidin)

     

    Abstract: Objective To study effects of epigallocatechin-3-gallate ( EGCG) on hepcidin mRNA in liver of mice with alcoholic liver disease (ALD) and to explore its mechanism.Methods C57/BL6 mice were randomly divided into a normal group and a model group. Alcoholic liver disease was induced by gavage of alcohol for 12 weeks.At the end of 8 weeks,the alcohol group was divided into a model group and three EGCG groups(10,20,and 30 mg·kg-1).The mice in the EGCG groups received an intraperitoneal injection of EGCG and simultaneous intragastric administration of alcohol for 4 weeks.Liver injuries were assessed with histopathologic examination and serum alanine aminotransferase (ALT),aspartate aminotransferase (AST) levels.In addition,liver iron levels were evaluated.Hepcidin mRNA in liver tissue was also determined with real-time PCR.Results The mice in model group had marked increases in serum ALT,AST levels and liver iron concentration compared with normal group,and their liver tissues showed moderate hepatocyte fatty degeneration.But the mice in EGCG groups had decreased ALT,AST levels and liver iron concentration and improved pathological changes.Liver hepcidin mRNA expression level was decreased significantly in model group compared with the normal group,but markedly increased in EGCG treatment groups.Conclusion Compared with model group,the hepcidin mRNA expression in livers of EGCG treatment ALD mice increases,and EGCG may play a protective role in the development of ALD.The possible mechanism of the effect may relate to EGCG inhibiting iron absorption in small intestine by the upregulation of hepcidin.

     

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