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作 者:周永列[1] 吕亚萍[2] 胡惟孝[2] 邱莲女[1] 王文松[1] 杨忠愚[2] 刘建栋[1]
机构地区:[1]浙江省人民医院中心实验室,浙江杭州310014 [2]浙江工业大学药学院,浙江杭州310014
出 处:《中国药理学通报》2006年第6期754-759,共6页Chinese Pharmacological Bulletin
基 金:浙江省科技厅资助项目(No2003c33019)
摘 要:目的观察四嗪二甲酰胺(ZGDHu-1)体外抑制肝癌细胞株HepG2增殖并诱导细胞凋亡作用。方法将不同浓度的ZGDHu-1与HepG2细胞在体外培养,用台盼蓝染色、MTT法、5′-溴-2′脱氧尿苷(B rdu)-ELISA法观察ZGDHu-1对HepG2细胞增殖的抑制作用;用细胞形态学、DNA凝胶电泳、DNA含量及细胞周期分析、Annexin-V/PI双标记、Ho-echst33258荧光染色和ELISA法测定DNA片段等技术检测细胞凋亡。结果ZGDHu-1能抑制HepG2细胞增殖和活力,呈现作用时间和剂量的量效关系。HepG2细胞与ZG-DHu-1作用后,大部分细胞阻滞于G2-M期;出现典型的细胞形态改变,DNA片断化,亚G1峰检出并增加,Annexin V+/PI-表达升高,细胞内DNA片段含量增加,Hoechst33258荧光染色后出现凋亡细胞的特征性改变等均证实ZGDHu-1能诱导HepG2细胞凋亡。结论ZGDHu-1能抑制HepG2细胞增殖,并可诱导其细胞凋亡。Aim To study the effect of N,N'-di-( m-methylphenyl) -3,6-dimethyl- 1,4-dihydro- 1,2,4,5-tetrazine-1,4-diearboamide ( ZGDHu-1 ) on proliferation inhibition and apoptosis in HepG2 cells in vitro. Method Different concentration of ZGDHu-1 and the different time of cultivate were used to treat HepG2 cell. The proliferation inhibition was analysed by alive cell count, MTI? assay and Brdu-ELISA. Cell apoptosis was analysed by cell morphology, DNA agarose gel eleetrophoresis, DNA content, Annexin-V/PI , cellular DNA feagmentation ELISA and Hoeehst33258 labeling method. Results ZGDHu-1 can inhibit HepG2 cell proliferation viability within a certain range of treating time and does,and a majority of HepG2 cells were arrested in G2/M phase. The HepG2 cells apoposis was comfirmed by type cell morphology and DNA fragment and sub-G1 phase and Hoechst33258 and Annexin/PI Labelingmethod and cellular DNA feagmentation ELISA with a time and does related manner. Conclusion ZGDHu-1 can inhibit proliferation and induced apoptosis of HepG2 cells.
关 键 词:四嗪二甲酰胺 肝癌 细胞株 HepG2 增殖 细胞凋亡
分 类 号:R329.24[医药卫生—人体解剖和组织胚胎学] R329.25[医药卫生—基础医学]
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