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二氢青蒿素抑制大鼠胶质瘤C6细胞增殖和诱导凋亡
引用本文:马振秋,黄晓佳,张纬萍,卢韵碧,魏尔清. 二氢青蒿素抑制大鼠胶质瘤C6细胞增殖和诱导凋亡[J]. 浙江大学学报(医学版), 2007, 36(3): 267-272
作者姓名:马振秋  黄晓佳  张纬萍  卢韵碧  魏尔清
作者单位:浙江大学医学院药理学教研室,浙江,杭州,310058
摘    要:目的:研究二氢青蒿素(dihydroartemisinin,DHA)对大鼠胶质瘤细胞(C6细胞)增殖和凋亡的影响。方法:在培养的C6细胞,加入DHA1~125μmol/L作用24、48、72h。以台盼蓝染色计数和噻唑蓝(MTT)还原反应,观察细胞增殖和活性;以Hoechst33342染色,观察细胞凋亡;以H2DCFDA氧化试验检测细胞内活性氧自由基(reactive oxygen species,ROS)变化。结果:DHA5~125μmol/L浓度及时间依赖性抑制C6细胞的增殖,作用48h后的IC50是23.4μmol/L;5~25μmol/L能诱导细胞凋亡(P<0.05);5~125μmol/L DHA可增高细胞内的ROS(P<0.01)。结论:DHA能够抑制C6细胞增殖,并诱导其凋亡,其细胞毒作用与细胞内ROS增加相关。

关 键 词:青蒿素/药理学  神经胶质瘤/药物疗法  活性氧  细胞增殖/药物作用  细胞凋亡/药物作用  肿瘤细胞,培养的
文章编号:1008-9292(2007)03-0267-06
收稿时间:2006-11-24
修稿时间:2007-04-10

Dihydroartemisinin inhibits proliferation and induces apoptosis of rat glioma C6 cells
MA Zhen-qiu,HUANG Xiao-jia,ZHANG Wei-ping, et al. Dihydroartemisinin inhibits proliferation and induces apoptosis of rat glioma C6 cells[J]. Journal of Zhejiang University. Medical sciences, 2007, 36(3): 267-272
Authors:MA Zhen-qiu  HUANG Xiao-jia  ZHANG Wei-ping   et al
Affiliation:Department of Pharmacology, College of Medicine, Zhejiang University, Hangzhou 310058, China.
Abstract:OBJECTIVE: To determine the effects of dihydroartemisinin (DHA) on the proliferation and apoptosis of rat glioma C6 cells. METHODS: DHA (1~ 125 micromol/L) was added into the cultured C6 cells and incubated for 24, 48 and 72 h. The cell proliferation and viability were determined by trypan blue exclusion assay and 3-(4, 5-dimethylthiazol-2yl)-2, 5 diphenyl tetrazolium bromide (MTT) reduction assay. The apoptosis was detected by Hoechst 33342 staining. The intracellular reactive oxygen species (ROS) was measured by H(2)DCFDA oxidative reaction. RESULTS: DHA 5 ~ 125 micromol/L inhibited the proliferation of C6 cells in concentration- and time-dependent manners, the IC50 at 48 h was 23.4 micromol/L. DHA 5 ~ 25 micromol/L induced C6 cell apoptosis (P<0.05), and 5 ~ 125 micromol/L increased the intracellular ROS (P<0.01). CONCLUSION: DHA inhibits the proliferation and induces the apoptosis of C6 cells; its cytotoxic effect may result from the increase of intercellular ROS.
Keywords:ARTEMISININ/pharmacol  Glioma/drug ther  Reactive oxygen species  Cell proliferation/ drug eff  Apoptosis/ drug eff  Tumor cells  cultured
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