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纪辉, 任立群, 张一宁, 李相军, 石艳, 迟宝荣. 姜黄素对肝星状细胞增殖能力影响[J]. 中国公共卫生, 2009, 25(4): 426-427. DOI: 10.11847/zgggws2009-25-04-21
引用本文: 纪辉, 任立群, 张一宁, 李相军, 石艳, 迟宝荣. 姜黄素对肝星状细胞增殖能力影响[J]. 中国公共卫生, 2009, 25(4): 426-427. DOI: 10.11847/zgggws2009-25-04-21
JI Hui, REN Li-qun, ZHANG Yi-ning, . Effects of curcumin on proliferation of hepatic satellite cell in vitro[J]. Chinese Journal of Public Health, 2009, 25(4): 426-427. DOI: 10.11847/zgggws2009-25-04-21
Citation: JI Hui, REN Li-qun, ZHANG Yi-ning, . Effects of curcumin on proliferation of hepatic satellite cell in vitro[J]. Chinese Journal of Public Health, 2009, 25(4): 426-427. DOI: 10.11847/zgggws2009-25-04-21

姜黄素对肝星状细胞增殖能力影响

Effects of curcumin on proliferation of hepatic satellite cell in vitro

  • 摘要: 目的探讨姜黄素对体外培养大鼠肝星状细胞细胞株(CSFSC-2G)增殖能力及细胞外基质分泌的影响。方法四甲基偶氮噻唑蓝(MTT)法检测不同浓度姜黄素(5,10,15,20,40μmol/L)在不同培养时间作用下肝星状细胞(HSC)的增殖能力;酶联免疫吸附实验法检测不同浓度姜黄素作用下HSCI型胶原(CollagenI,ColI)和Ⅲ型胶原(CollagenⅢ,ColⅢ)合成及分泌能力;流式细胞术检测姜黄素对HSC凋亡的影响。结果不同浓度的姜黄素(5,10,15,20,40μmol/L)均可抑制HSC增殖,并呈现明显剂量依赖关系;含20μmol/L姜黄素培养基培养24h后,HSC-ColI、ColⅢ吸光度(A)值分别为(0.418±0.019),(0.554±0.043),均明显低于阴性对照组,差异有统计学意义(P<0.05);含20μmol/L姜黄素培养基培养48h后,HSC处于G0/G1期的HSC细胞占(39.98±8.07)%,S期细胞占(55.79±9.13)%,G2/M期细胞占(4.23±0.12)%;凋亡率为(20.31±2.55)%,高于阴性对照组凋亡率(0.22±0.11)%,低于秋水仙素阳性药物对照组凋亡率(29.75±2.64)%,差异均有统计学意义(P<0.05)。结论姜黄素可抑制HSC细胞的增殖并促进其凋亡,有可能成为防治肝纤维化的理想药物。

     

    Abstract: Objective To investigate the effects of curcumin on proliferation and collagen(col)secretion of hepatic satellite cells in vitro.Methods CSFSC-2G were incubated with different concentration of curcumin(0,5,10,15,20,40 μmol/L)for different times(6h,12h,24h,48h and 72h).MTT was used for the detecting of proliferation of HSC.Col Ⅰ and Col Ⅲ were determined by ELISA and flowcytometry was applied to evaluate apoptosis of HSC.Results Curcumin inhibited the proliferation of HSC with dose-dependent manner,especially in 20 and 40 μmol/L curcumin groups at 24h.When HSC was cultured after 24h,the absorbency of Col Ⅰ and Col Ⅲ in 20 μmol/L curcumin group was 0.418±0.019 and 0.554±0.043,respectirely,both lower than those of 0 μmol/L curcumin group significantly(P<0.01).When HSC was cultured after 48h,the ratio of apoptosis in 20 μmol/L curcumin group was 20.31%±2.55% and higer than that of 0 μmol/L curcumin group significantly(P<0.01).Conclusion Curcumin can delay liver fibrosis not only by inhibiting the proliferation and stimulating apoptosis of HSC,but also by decreasing Col Ⅰ and Col Ⅲ secretion.

     

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