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作 者:喻冬柯[1,2] 张胜华[2] 邵荣光[2] 何红伟[2]
机构地区:[1]四川省医学科学院四川省人民医院,成都610072 [2]中国医学科学院医药生物技术研究所,北京100050
出 处:《中国新药杂志》2015年第2期143-147,共5页Chinese Journal of New Drugs
基 金:国家"重大新药创制"科技重大专项(2012ZX09301002-001);国家自然科学基金(81170409);中国肝炎防治基金会王宝恩肝纤维化研究基金(20110026);四川省医学科学院四川省人民医院博士基金(30305030828)
摘 要:目的:利用大鼠全基因组芯片检测表没食子儿茶素没食子酸酯(EGCG)对胆管结扎肝纤维化大鼠基因表达的影响并进行评价和研究。方法:使用胆管结扎的方法造胆汁淤积型的肝纤维化大鼠模型,并提取假手术组、模型组和给药组大鼠肝脏的总RNA,用大鼠全基因组芯片法分析其基因组表达谱的变化。结果:基因芯片结果显示,有626个基因同时在EGCG给药组与模型组发生变化,其中327个基因下调,299个基因上调。EGCG逆转了很多基因的表达变化,其中包括胆汁代谢通路、脂代谢、糖代谢等多种代谢相关通路、免疫相关通路等。此外,EGCG还影响多条肝纤维化相关的信号通路中相关基因的变化。结论:EGCG对胆汁淤积型肝纤维化大鼠模型的肝纤维化有抑制作用,该作用可能是通过调节多个肝纤维化相关的信号通路来发挥的。Objective: To investigate the role of epigallocatechin gallate( EGCG) in the regulation of gene expression of liver fibrosis rats. Methods: Liver fibrosis rat model was induced by bile duct-ligation( BDL). The total RNA was isolated from the rats in sham-operation group,liver fibrosis model group,and EGCG group,and then screened for the differently expressed genes with gene chip technique. Results: The results of gene chip screening showed that there were 327 genes down-regulated and 299 genes up-regulated in the EGCG group compared to the liver fibrosis model group. These genes were related to bile acid biosynthesis,lipid metabolism,glucose metabolism pathway,immune-related pathways,and so on. EGCG also had effect on some liver fibrosis related pathway. Conclusion: EGCG has inhibition effect on the liver fibrosis of bile duct-ligated rat model,and the mechanism may be related to regulation of multiple signaling pathways.
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