期刊文献+

清胆胶囊对胆石病C57小鼠肝脏基因表达谱的影响 被引量:5

Effects of "Qingdan Capsule" on liver gene expression profiles in C57 mice with cholelithiasis
原文传递
导出
摘要 目的探讨清胆胶囊对胆石病C57小鼠肝脏基因表达谱的影响。方法将38只SPF级C57BL/6J雌性小鼠随机分为对照组(n=10)、模型组(n=15)及清胆胶囊组(n=13)。对照组喂以正常饲料,模型组和清胆胶囊组喂以高脂致石饲料,其中清胆胶囊组在予高脂饮食的同时,予清胆胶囊干预。于实验第8周末处死,应用Oligo GEArray芯片检测肝脏基因表达的改变。结果与对照组比较,模型组出现显著差异表达的基因共35条,上调基因34条,下调基因1条,为Col3a1;与模型组比较,清胆胶囊组出现显著差异表达的基因38条,其中下调基因36条,上调基因2条,为Il3和Ppard;与模型组比较,对照组和清胆胶囊组同时下调两倍的基因27条,主要为代谢酶相关基因、脂肪酸结合蛋白基因、炎症和纤维化相关基因等。结论从基因学角度分析显示,清胆胶囊可以改善肝脏的炎症损伤,减少胆汁中胆固醇结晶的形成,降低结石形成的几率。 Objective To observe the effects of "Qingdan Capsule" on liver gene expression profiles in C57 mice with cholelithiasis.Methods Thirty-eight SPF C57BL/6J female mice were randomly divided into three groups: control group in which 10 mice were fed normal diet,model group in which 15 mice were fed high-fat diet and treatment group in which 13 mice were fed high-fat diet and "Qingdan Capsule".All mice were sacrificed at the 8th week and hepatic gene expression was detected with Genechip Oligo GEArray〖XCR.tif;%70%70〗.Results Compared with control group,the number of significant different expression genes in model group was 35 including 34 of up-regulated genes and 1 down-regulated gene(Col3a1);compared with model group the number of significant different expression genes in treatment group was 38 including 36 of down-regulated genes and 2 up-regulated genes(Il3 and Ppard);compared with model group the number of down-regulated genes in treatment group and control group was 27,such as metabolic enzyme genes,fatty acid binding protein genes,inflammatory genes and fibrosis genes.Conclusion Treatment of cholelithiasis with "Qingdan Capsule" can relieve inflammation,reduce the cholesterol crystallization in bile and lower risk of gallstone formation.
出处 《上海中医药杂志》 2011年第5期78-81,86,共5页 Shanghai Journal of Traditional Chinese Medicine
基金 上海市医学领军人才资助课题(LJ06048) 上海市科委自然科学基金项目(09ZR1432300) 上海市教育委员会科研创新项目(09YZ131)
关键词 高脂饮食 胆石病 基因 清胆胶囊 High-fat diet cholelithiasis gene "Qingdan Capsule"
  • 相关文献

参考文献9

  • 1周爱儒.生物化学[M].北京:人民卫生出版社,2003.406-413.
  • 2Schwartz CC, Berman M, Vlahcevic ZR, et al. Multicompartmental a- nalysis of cholesterol metabolism in man . Characterization of the hepatic bile acid and biliary cholesterol precursor sites [J].J Clin Genet, 1978, 61 (2) :408-423.
  • 3Mitchell JC, Stone BG, Logan GM, et al. Role of cholesterol synthesis in regulation of bile acid synthesis and biliary cholesterol secretion in hu- man [ J ]. J Lipid Res, 1991,32 ( 7 ) : 1143-1149.
  • 4Rudel L, Deckelman C, Wilson M, et al. Dietary cholesterol and down- regulation of cholesterol 7 alpha-hydroxylase and cholesterol absorption in African green monkeys[ J], J Clin Invest, 1994,93 (6) :2463-2672.
  • 5金伯泉.细胞和分子免疫学[M].北京:科学出版社,2006:61,135-136,572.
  • 6韩天权,蒋兆彦,张圣道.胆石病人肠肝循环途径脂质代谢异常的分子生物学研究进展[J].中华肝胆外科杂志,2008,14(4):219-220. 被引量:8
  • 7王蕾,蒋兆彦,胡海,所广军,袁耀宗,江石湖,张圣道,韩天权.肝脏肝X受体α和雌激素受体α表达与女性胆石病关系的研究[J].诊断学理论与实践,2006,5(4):308-311. 被引量:8
  • 8梁晓强,章学林,顾宏刚,张静喆.养肝利胆颗粒对胆色素结石炎症反应环节的影响[J].中国中西医结合消化杂志,2009,17(2):102-104. 被引量:2
  • 9陈孝平.外科学[M].北京:人民出版社,2005:58.

二级参考文献22

  • 1蒋兆彦,韩天权,所广军,袁作彪,姜志宏,商俊,蔡杏兴,Gsta Eggertsen,Curt Einarsson,张圣道.胆固醇结石病人肝脏胆小管侧膜ATP基因表达差异的研究[J].外科理论与实践,2005,10(1):61-65. 被引量:24
  • 2张静喆.肝胆管结石的中西医结合治疗[J].肝胆胰外科杂志,2006,18(3):137-138. 被引量:3
  • 3顾宏刚,张静喆,章学林,刘建文,李婷,朱培庭.升清胶囊对胆色素结石豚鼠肝细胞核因子-κB蛋白表达的影响[J].中西医结合学报,2006,4(5):518-521. 被引量:9
  • 4关中正,唐乾利.胆色素结石形成的因素研究进展[J].菏泽医学专科学校学报,2007,19(1):68-73. 被引量:8
  • 5朱培庭 张静哲 等.治疗慢性胆道感染、胆石病274例的总结[J].上海中医药杂志,1986,(9):15-15.
  • 6汤文浩 韩天权 等.测定胆汁胆固醇和磷脂的简捷方法[J].上海医学检验杂志,1994,9:122-122.
  • 7JAVANTHI V, ANAND L, ASHOK L, et al. Dietary factors in pathogenesis of gallstone disease in southern India-a hospital_based case control study[J]. Indian J Gastroenterof , 2005,24: 97-- 99.
  • 8STEWART L, OESTERLE A L, ERDAN I, et al. Pathogenesis of pigment gallstones in Western societies: the central role of bacteria [J]. J Gastrointest Surg,2002,6:891--903.
  • 9JUNGST C, SREEJAYAN N, EDER M I, et al. Lipid peroxidation and muein secretagogue activity in bile of gallstone patients[J]. Eur J Clin Invest, 2007,37:731 -736.
  • 10LI J J, FENG C H. C-reactive protein is not only an inflammatory marker but also a direct cause of cardiovascular disease[J]. Med Hypothese, 2004,62: 499-- 506.

共引文献413

同被引文献40

引证文献5

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