期刊文献+

乳黄制剂对肝硬化模型大鼠晚期糖基化终末产物(AGEs)的影响 被引量:1

Ruhuang Preparation on Advanced Glycation Endproducts(AGEs) in Cirrhotic Rats
下载PDF
导出
摘要 目的观察乳黄制剂对肝硬化模型大鼠晚期糖基化终末产物(AGEs)的影响。方法用四氯化碳(CCl4)复合因素法制造肝硬化模型大鼠,分组治疗后观察肝脏组织病理学变化,用酶联免疫分析法(ELISA)定量测定大鼠肝组织匀浆AGEs的含量。结果乳黄制剂可明显降低肝硬化模型大鼠AGEs含量水平(P<0.05);预防组和模型治疗组肝组织的肝硬化以及纤维组织增生、炎性细胞浸润程度得到改善,其中预防组肝组织的病理变化改善明显。结论乳黄制剂能有效降低肝组织中AGEs的水平,有利于肝硬化程度的好转。 Objective On the existing experimental basis,to further study Ruhuang preparation on liver cirrhosis rat model advanced glycation end products(AGEs).Methods The composite factor method CCl4 cirrhotic rats manufacturing to AGEs content in liver homogenates and liver pathology as the index,using enzyme-linked immunosorbent assay(ELISA) quantitative analysis of liver tissue homogenate content of AGEs.Results Ruhuang preparation can significantly reduce the milk of rats with liver AGEs concentration levels(P0.05);to improve the treatment group and model group to prevent liver cirrhosis and fibrosis,inflammatory cell infiltration,including the prevention of liver tissue The pathological changes were improved.Conclusion Ruhuang preparation can reduce the level of AGEs in liver tissue,is beneficial for the improvement of liver cirrhosis.
出处 《湖北中医学院学报》 2010年第6期11-13,共3页 Journal of Hubei College of Traditional Chinese Medicine
关键词 乳黄制剂 肝硬化 晚期糖基化终末产物 实验研究 Ruhuang Preparation Cirrhosis Advanced Glycation End Products Experimental study
  • 相关文献

参考文献7

二级参考文献57

共引文献101

同被引文献15

  • 1詹可顺,王华,魏伟.白芍总苷对小鼠化学性肝损伤的保护作用及机制[J].安徽医科大学学报,2006,41(6):664-666. 被引量:42
  • 2周艳丽,张磊,刘维.白芍总苷对雷公藤多苷片所致小鼠急性肝损伤保护作用的实验研究[J].天津中医药,2007,24(1):61-62. 被引量:67
  • 3SU J, ZHANG P, ZHANG J J, et al. Effects of total glucosides of paeony on oxidative stress in the kidney from diabetic rats [ J ]. Phytomedicine, 2010, 17 ( 3/4 ) : 254 - 260.
  • 4VELAYUDHAM A,DOLQANIUC A,ELLIS M,et al. VSL#3 probiotic treatment attenuates fibrosis without changes in steatohepatitis in a diet-induced nonalcoholic steatohepatitis model in mice [ J ]. Hepatology,2009,49 ( 3 ) :989 - 997.
  • 5OUYANG Xiao-sen, CIRILLO P, SAUTIN Y,et al. Fructose consumption as a risk factor for non-alcoholic fatty liver disease [ J]. J Hepatol,2008,48:993 - 999.
  • 6VOLYNETS V, SPRUSS A, KANURI G, et al. Protective effect of bile acids on the onset of fructose-induced hepatic steatosis in mice[ J]. J Lipid Res ,2010,51:3413 - 3424.
  • 7UTZSCHNEIDER K M, KAHN S E. Review: the role of insulin resistance in nonalcoholic fatty liver disease [ J ]. J Clin Endocr Metab ,2006,91 ( 12 ) :4753 - 4761.
  • 8DAY C Y,JAMES O F. Steatohepatitis a tale of two "hits" [ J ]. Gastroenterology, 1998,114:842.
  • 9GENTILE C L, PAGLIASSOTTI M J. The role of fatty acids in the development and progression of nonalcoholic fatty liver disease [ J ]. J Nutr Biochem ,2008 ,19 : 568.
  • 10BROWNING J D, HORTON J D. Molecular mediators of hepatic steatosis and liver injury [ J]. J Clin Invest,2004, 114(2) :147 - 152.

引证文献1

二级引证文献21

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