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机构地区:[1]上海医药工业研究院国家上海新药安全评价研究中心 [2]浙江康乐药业有限公司,温州325028
出 处:《中国新药杂志》2007年第3期193-196,共4页Chinese Journal of New Drugs
摘 要:目的:研究威替米星和庆大霉素对体外培养的人肾小管上皮细胞系(HK-2)毒性作用的分子机制。方法:利用基因芯片技术检测3.2 mg.mL-1威替米星和庆大霉素作用于HK-2细胞48 h后基因表达的变化。结果:威替米星诱导HK-2细胞87个基因发生显著的上调,10个基因发生明显的下调。庆大霉素则引起62个基因表达显著上调,18个基因明显下调。差异表达的基因的功能涉及细胞生长增殖调控、凋亡、细胞周期、应激反应、转运及代谢酶等方面。结论:威替米星和庆大霉素改变细胞凋亡、应激反应及转运等相关基因表达可能参与其细胞毒性作用过程。Objective :To investigate the effects of vertilmicin and gentamicin on gene expression of human renal tubular epithelial cell lines (HK-2). Methods: Gene expression profiles were identified by DNA microarrays in HK-2 cells exposed to vertilmicin and gentamicin (3.2 mg· mL^-1 ) for 48 h, respectively. Results: Vertilmicin significantly upregulated 87 genes and downregulated 10 genes of HK-2 cells. Gentamicin significantly upregulated 62 genes and downregulated 18 genes of HK-2 cells. The expressions of the various genes modulated cell growth and proliferation, apoptosis, cell cycle, stress response, transporters, chaperones, transcription regulation and drug metabolism. Conclusion: The alteration of these specific genes that regulated cellular apoptosis, stress response and transportation may be associated with cytotoxicity of aminoglycosides.
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