期刊文献+

EGCG对酒精性肝病小鼠肝脏铁调素表达影响 被引量:2

Effects of epigallocatechin-3-gallate on expression of hepcidin mRNA in liver of mice with alcoholic liver disease
原文传递
导出
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,EGCG10、20、30mg/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—timePCR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hepcidinmRNA[0.051±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。 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 im- proved 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.
出处 《中国公共卫生》 CAS CSCD 北大核心 2014年第3期305-307,共3页 Chinese Journal of Public Health
基金 广西自治区教育厅项目(200103YB090) 桂林医学院"项目驱动教学法"专项课题
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) epigallocatechin-3-gallate alcoholic liver disease iron overload hepcidin
  • 相关文献

参考文献6

  • 1Harrison-findik DD, Klein E, Evans J, et al. Regulation of liver hepcidin expression by alcohol in vivo does not involve Kupffer cell activation or TNF-alpha signaling [ J ]. Am J Physiol Gas- trointest Liver Physio1,2009,296 : 112 - 118.
  • 2Ohtake T,Saito H ,Hosoki Y,et al. Hepcidin is down-regulated in -al- cohol loading[J]. Alcohol Clin Exp Res,2007,31 (1):S2-8.
  • 3Bridle K,Chetng TK,Murphy T,et al. Hepcidin is down-regulated in alcoholic liver injury: implications for the pathogenesis of alcoholic liver disease[ J]. Alcohol Clin Exp Res,2006,30 ( 1 ) : 106 - 112.
  • 4Nicolas G,Bennoun M,Porteu A,et al. Severe iron deficiency a- nemia in transgenic mice expressing liver hepcidin [ J ]. Proc Natl Acad Sci USA,2002,99:4596-4601.
  • 5李相武,童玲玲,李东阳.茶多酚对人肝癌细胞激活蛋白1及细胞周期影响[J].中国公共卫生,2006,22(3):327-328. 被引量:4
  • 6刘甜甜,赵海峰.植物化学物对阿尔茨海默病保护作用研究进展[J].中国公共卫生,2013,29(5):772-775. 被引量:8

二级参考文献24

  • 1王佩,王海祥,王维平.突触可塑性与学习记忆[J].脑与神经疾病杂志,2008,16(5):651-653. 被引量:8
  • 2Gansauge S,Gansauge F,Ramadani M,et al.Overexpression of cyclinD1 in human pancreatic carcinoma is associated with poor prognosis[J].Cancer Research,1997,57(9):1634-1637.
  • 3Hsu TC,Yong MR,Cmarik J,et al.Activator protein 1(AP-1)-and nuclear factor kappaB(NF-kappaB)-dependent transcriptional events in carcinogenesis[J].Free Radic Biol Med,2000,28(9):1338-1348.
  • 4Yang GY,Liao J,Li C,et al.Effect of black and green tea polyphenols on c-jun phosphorylation and H(2)O(2)production in transformed and non-transformed human bronchial cell lines:possible mechanisms of cell growth inhibition and apoptosis induction[J].Carcinogenesis,2000,21(11):2035-2039.
  • 5Nomura M,Ma WY,Huang C,et al.Inhibition of ultraviolet B-induced AP-1 activation by theaflavins from black tea[J].Mol Carcinog,2000,28(3):148-155.
  • 6Albanese C,D Amico M,Reatens AT,et al.Activation of the cyclinD1 gene by the E1A-associated protein p300 through AP-1 inhibits cellular apoptosis[J].Biol Chem,1999,274(48):34186-34195.
  • 7Bakiri L,Lallemand D,Bossy Wetzel E,et al.Cell cycle-dependent variations in c-jun and c-junB phosphorylation:a role in the control of cyclinD1 expression[J].Euro Mol Biol Org,2000,19(9):2056-2068.
  • 8沈丽霞,牛建昭,王继峰.槲皮素对AlCl_3致衰老模型小鼠记忆障碍的保护作用[J].北京中医药大学学报,2007,30(9):615-617. 被引量:6
  • 9张红梅,李昱.植物提取物治疗阿尔茨海默病的研究进展[J].国际神经病学神经外科学杂志,2007,34(6):531-534. 被引量:3
  • 10龙燕,左丽,李光荣,裴华,赵明祥.阿尔茨海默病与EB病毒及ApoE基因多态性关系[J].中国公共卫生,2008,24(5):573-574. 被引量:2

共引文献10

同被引文献42

引证文献2

二级引证文献35

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部