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机构地区:[1]广州医科大学附属肿瘤医院药学部,广州510095
出 处:《中国药房》2015年第16期2190-2192,共3页China Pharmacy
摘 要:目的:研究复方苦参注射液对人肝癌SMMC7721细胞增殖的抑制作用。方法:体外传代培养SMMC7721细胞。10、20、40、80、160μl/ml复方苦参注射液培养细胞24、48、72 h后,采用MTT法测定细胞活力并计算抑制率。0(阴性对照)、10、20、40、80、160μl/ml复方苦参注射液培养细胞48 h后采用流式细胞仪测定细胞凋亡率,并分析细胞周期分布百分比。结果:10、20、40、80、160μl/ml复方苦参注射液培养细胞24、48、72 h对细胞具有明显的抑制作用,且具有时间和剂量依赖性。与阴性对照比较,40、80、160μl/ml复方苦参注射液培养细胞48 h后,G0/G1期细胞比例明显升高(P<0.05),S期细胞比例明显降低(P<0.05),细胞凋亡率明显升高(P<0.05)。结论:复方苦参注射液对SMMC7721细胞的增殖具有抑制作用,其机制可能是诱导细胞凋亡、阻滞细胞于G0/G1期。OBJECTIVE: To study the inhibitory effects of Compound kushen injection on the proliferation of human hepatoma SMMC7721 cells. METHODS: Human hepatoma cell line SMMC7721 was subcultured in vitro. MTT assay was adopted to deter- mine cell viability after the cells were cultured in 10μl/ml, 20μl/ml, 40μl/ml, 80μl/ml and 160μl/ml Compound kushen injec- tion for 24 h, 48 h and 72 h, and the inhibition rates were calculated. The apoptosis rates was determined after the cells were cul- tured in 0 (negative control), 10 μl/ml, 20μl/ml, 40μl/ml, 80 μl/ml and 160μl/ml Compound kushen injection for 48 h,and the cells were cultured therein for 48 h, and percentage of cell cycle distribution was analyzed. RESULTS: After the cells were cul- tured in 10μl/ml, 20μl/ml, 40μl/ml, 80μl/ml and 160μl/ml Compound kushen injection for 24 h, 48 h and 72 h, the injection showed obvious inhibitory effect on the cells with time and dose-dependence. Compared with negative control group, the proportion of the cells in G0/G1 phase was obviously increased (P〈0.05) and that of the cells in S phase was obviously decreased (P〈0.05), and the apoptosis rates of the cells were obviously increased(P〈0.05) after the cells were cultured in 40μl/ml, 80 μl/ml and 160 μl/ml Compound kushen injection for 48 h. CONCLUSIONS: Compound kushen injection have inhibitory effects on the prolifera- tion of SMMC7721 cells by a mechanism that may be related to the induction of apoptosis and G0/G1 cell cycle arrest.
关 键 词:复方苦参注射液 人肝癌SMMC7721细胞 细胞增殖 凋亡
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