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cDNA基因芯片技术分析三聚氰胺肾毒性的相关基因表达
引用本文:时美,范雪梅,李雪,王铮,王义明,罗国安. cDNA基因芯片技术分析三聚氰胺肾毒性的相关基因表达[J]. 高等学校化学学报, 2010, 31(4): 684-689
作者姓名:时美  范雪梅  李雪  王铮  王义明  罗国安
作者单位:华东理工大学药学院,上海,200237;清华大学中药现代化研究中心,北京,100084;南开大学药学院,天津,300071;华东理工大学药学院,上海,200237;清华大学中药现代化研究中心,北京,100084
基金项目:国家九七三计划项目,国家十一五科技支撑项目,教育部博士点基金 
摘    要:利用基因芯片技术筛查不同剂量的三聚氰胺干预大鼠肾脏的差异表达基因, 并对筛查的差异基因进行生物信息学分析, 推测三聚氰胺肾毒性的分子作用机制. 结果表明, 高剂量三聚氰胺干预的大鼠肾脏差异表达基因数多于低剂量干预的肾脏差异表达基因, 并且涉及到更多重要的分子功能和代谢途径, 表明三聚氰胺肾毒性具有剂量依赖性, 相比低剂量而言, 高剂量三聚氰胺干预对肾脏的危害更为严重.

关 键 词:三聚氰胺  基因芯片  肾毒性  肾结石
收稿时间:2009-07-22

Gene Expression Studies of Melamine-related Renal Toxicity Based on cDNA Microarray
SHI Mei,FAN Xue-Mei,LI Xue,WANG Zheng,WANG Yi-Ming,LUO Guo-An. Gene Expression Studies of Melamine-related Renal Toxicity Based on cDNA Microarray[J]. Chemical Research In Chinese Universities, 2010, 31(4): 684-689
Authors:SHI Mei  FAN Xue-Mei  LI Xue  WANG Zheng  WANG Yi-Ming  LUO Guo-An
Affiliation:1. School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China;2. Modern Research Center of TCM, Tsinghua University, Beijing 100084, China;3. School of Pharmacy, Nankai Universities, Tianjin 300071, China
Abstract:Nowadays, microarray technology has been used in toxicogenomics more and more often. In this paper, we applied it into the renal toxicity research of melamine, which is an intermediate of resin in chemical industry. The experimental, through microarray and bioinformatics, was designed to find the differences between two cases in which the rats independently intervened by high and low doses melamine, and then to interpret the molecular mechanism of renal toxicity. The result indicated that the number of differentially expressed genes intervened by high dose of melamine were more than that by low dose of melamine. Besides, the differential expressed genes interfered by high dose melamine have been proved to have close connection with some important pathways as follow: valine, leucine and isoleucine degradation, citrate metabolism, glutathione metabolism, fatty acid metabolism, and the molecular function such as mental binding, lyase activity, ligase activity, symporter activity, glutathione transferase activity, monooxygenase activity. Our research show the toxicity in kidney intervened by melamine, and demonstrated the special advantage of microarray technology in toxicogenomics.
Keywords:Melamine   Microarray   Nephrotoxicity   Nephrolithiasis
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