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党参皂苷D对HepG-2细胞增殖时间效应和细胞周期的影响
引用本文:俞星,韩春姬,朴惠善,李琚.党参皂苷D对HepG-2细胞增殖时间效应和细胞周期的影响[J].吉林大学学报(医学版),2012,38(2):236-240.
作者姓名:俞星  韩春姬  朴惠善  李琚
作者单位:延边大学基础医学院生理学教研部,吉林延吉133002;延边大学基础医学院预防医学教研部,吉林延吉133002;延边大学基础医学院预防医学教研部,吉林延吉,133002;延边大学药学院药物化学教研部,吉林延吉,133002
基金项目:国家科技部国际合作专项基金资助课题,吉林省科技发展计划项目资助课题
摘    要:目的:观察党参皂苷D对HepG-2细胞增殖时间效应和细胞周期的影响,探讨轮叶党参抗癌活性成分及作用机制。方法:不同浓度(5、10、15、20和25 mg/L)党参皂苷D作用于体外培养的人肝癌HepG-2细胞,同时设空白对照组;采用 MTT法检测党参皂苷D对HepG-2细胞增殖抑制情况,流式细胞术检测细胞周期变化。结果:25 mg/L党参皂苷D作用12、24、48
和72 h后,HepG-2细胞增殖抑制率均明显高于对照组,差异有统计学意义(P<0.01)。党参皂苷D作用48、72、96及120 h后,各组细胞总数明显低于对照组,差异有统计学意义(P<0.05);党参皂苷D 5、15、20及25 mg/L组间比较,差异有统计学意义(P<0.05),且随着党参皂苷D浓度增加,HepG-2细胞增殖速度缓慢。细胞周期检测结果表明,党参皂苷D浓度为10、15、20和25 mg/L时,G0/G1期细胞所占百分比分别为55.97%±0.42%、57.16%±0.13%、57.48%±0.15%及60.39%±0.32%,与空白对照组(53.22%±0.28%)比较,差异均有统计学意义(P<0.05);此浓度范围内S期细胞所占百分比分别为27.47%±1.42%、26.15%±2.71%、26.34%±0.67%及24.81%±0.46%,与空白对照组(33.47%±0.25%)比较,差异均有统计学意义(P<0.05)。党参皂苷D组的细胞周期发生了G0/G1期阻滞。结论:党参皂苷D在体外明显抑制HepG-2细胞生长,并能引起癌细胞DNA合成代谢紊乱。

关 键 词:党参皂苷D  HepG-2  生长曲线  细胞增殖  细胞周期
收稿时间:2011-12-25

Effects of lancemaside D on time effect of proliferation and cell cycle of HepG-2 cells
YU Xing , HAN Chun-ji , PIAO Hui-shan , LI Ju.Effects of lancemaside D on time effect of proliferation and cell cycle of HepG-2 cells[J].Journal of Jilin University: Med Ed,2012,38(2):236-240.
Authors:YU Xing  HAN Chun-ji  PIAO Hui-shan  LI Ju
Institution:1.Department of Physiology|College of Basic Medical Sciences|Yanbian University|Yanji 133002|China;2.Department of Preventive Medicine|College of Basic Medical Sciences|Yanbian University|Yanji 133002|China;3.Department of Medicinal Chemistry|College of Pharmacy,Yanbian University|Yanji 133002|China
Abstract:Objective To investigate the effect of lancemaside D on the time effects of cell proliferation and cell cycle of HepG-2 cells and explore the anticancer active ingredients and mechanisms of codonopsis lanceolata.Methods The HepG-2 cells were treated with different concentrations(5,10,15,20 and 25 mg·L-1) of lancemaside D in vitro,meanwhile control group was set up.The proliferation inhibition of HepG-2 cells was detected by MTT assay,and the change of cell cycle of HepG-2 cells was determined by flow cytometry.Results The results showed that the inhibitory rate of cell proliferation of HepG-2 cells were significantly higher than that in control group(P<0.01) after treated with 25 mg·L-1 lancemaside D for 12,24,48 and 72 h;the cell numbers in lancemaside D groups were significantly smaller than that in control group after treated with lancemaside D for 48,72,96 and 120 h(P<0.05),among 5,15,20 and 25 mg·L-1groups there were significant differences(all P<0.05);the HepG-2 cell proliferation speed was delated with the increasing of lancemaside D concentration.The cell cycle detection results showed that in the lancemaside D concentration range of 10-25 mg·L-1,the percentages of HepG-2 cells at G0/G1 phase were 55.97%±0.42%,57.16%±0.13%,57.48%±0.15% and 60.39%±0.32%,respectively,they were significantly higher than that in control group(53.22%±0.28%)(P<0.05).In the same concentration range of lancemaside D,the percentages of HepG-2 cells at S phage were 27.47%±1.42%,26.15%±2.71%,26.34%±0.67% and 24.81%±0.46%,they were significantly lower than that in control group(33.47%±0.25%)(P<0.05),which suggested a G0/G1 cell cycle arresting in lancemaside D group.Conclusion Lancemaside D strongly inhibits the growth of HepG-2 cells in vitro and furthermore cause cell DNA metabolism disturbance.
Keywords:lancemaside D  HepG-2  growth curve  cell proliferation  cell cycle
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