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李彦坤, 李鑫, 彭洪, 王吉锡, 李洪源. 甘草提取物(GL-1)对Hela细胞增殖抑制及促凋亡作用[J]. 中国公共卫生, 2016, 32(9): 1186-1188. DOI: 10.11847/zgggws2016-32-09-14
引用本文: 李彦坤, 李鑫, 彭洪, 王吉锡, 李洪源. 甘草提取物(GL-1)对Hela细胞增殖抑制及促凋亡作用[J]. 中国公共卫生, 2016, 32(9): 1186-1188. DOI: 10.11847/zgggws2016-32-09-14
LI Yan-kun, LI Xin, PENG Hong.et al, . Anti-proliferative effect of Glycyrrhiza extraction on Hela cells and its mechanism[J]. Chinese Journal of Public Health, 2016, 32(9): 1186-1188. DOI: 10.11847/zgggws2016-32-09-14
Citation: LI Yan-kun, LI Xin, PENG Hong.et al, . Anti-proliferative effect of Glycyrrhiza extraction on Hela cells and its mechanism[J]. Chinese Journal of Public Health, 2016, 32(9): 1186-1188. DOI: 10.11847/zgggws2016-32-09-14

甘草提取物(GL-1)对Hela细胞增殖抑制及促凋亡作用

Anti-proliferative effect of Glycyrrhiza extraction on Hela cells and its mechanism

  • 摘要: 目的 提取甘草抗肿瘤成份(GL-1),探讨其对人宫颈癌HeLa细胞的增殖抑制及凋亡诱导作用。方法 通过水提法、丙酮萃取、甲醇分离提取得到甘草提取物GL-1,并通过液质连用技术分析其主要成分,通过MTT比色法观察GL-1对HeLa细胞增殖抑制作用;AO (吖啶橙)/EB (溴化乙锭)双荧光染色法检测HeLa凋亡情况;透射电镜观察细胞凋亡的形态学变化。结果 GL-1含有9种主要组成成份。GL-1对HeLa细胞的生长增殖有抑制作用,其作用于Hela细胞12、24、48 h的半数抑制浓度分别为51.90、22.30、16.10 μg/mL (P<0.05);AO/EB染色观察到25、50 μg/mL剂量组HeLa细胞均有不同程度的凋亡作用;透射电镜观察可见典型细胞凋亡形态。结论 GL-1具有抑制HeLa细胞生长增殖作用,并可诱导HeLa细胞凋亡。

     

    Abstract: Objective To isolate an active anti-tumor extraction from Glycyrrhiza (GL-1) and to investigate anti-proliferative and apoptosis induction effects of GL-1 on Hela cells.Methods By using water filtering,acetone-extraction and methanol purification,we extracted GL-1 from Glycyrrhiza;then main components of GL-1 were detected with high-performance liquid chromatography mass spectrometry (HPLC-MS).3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was adopted to determine the anti-proliferative effect of GL-1 on Hela cells.With double acridine orange/ethidium bromide (AO/EB) staining,we observed morphological change of Hela cells treated with GL-1.Transmission electronic microscope (TEM) was used to observe morphological change of typical apoptosis.Results GL-1 includes 9 main components.The result of MTT assay indicates that GL-1 has an obvious anti-proliferative effect on Hela cells.The half maximal inhibitory concentrations (IC50) of GL-1 were 51.90,22.30,and 16.10 μg/ml (P<0.05) for the treatment time of 12,24,and 48 hours,respectively.The results of AO/EB double staining assay showed that GL-1 could induce apoptosis in Hela cells.TEM observation revealed typical morphological apoptosis changes,including decreased nucleus/cytoplasm ratio,absence of nucleus,vacuoles in cytoplasm,condensed chromatin,and detachment of microvilli on cell membran.Conclusion GL-1 has an anti-proliferative effect on Hela cells and could induce apoptosis of Hela cells.

     

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