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山楂原花青素对人肝癌SMMC-7721细胞增殖和凋亡的影响
引用本文:孙思明,徐宏伟,郭凯元,郭梦冉,崔胜男,崔同,檀建新.山楂原花青素对人肝癌SMMC-7721细胞增殖和凋亡的影响[J].食品科学,2019,40(5):189-196.
作者姓名:孙思明  徐宏伟  郭凯元  郭梦冉  崔胜男  崔同  檀建新
作者单位:河北农业大学食品科技学院,河北省农产品加工工程技术研究中心,河北 保定 071001
基金项目:河北省自然科学基金项目(C2015204187);河北省重点研发计划项目(16275505D);河北省食品科学与工程学科“双一流”建设资金项目(2016SPGCA18)
摘    要:目的:探讨山楂原花青素提取物、表儿茶素和原花青素B2对人肝癌SMMC-7721细胞增殖及凋亡的影响。方法:体外培养SMMC-7721细胞,噻唑蓝法检测不同质量浓度山楂原花青素对细胞增殖的影响;4’,6-二脒基-2-苯基吲哚染色法观察细胞凋亡,Western blot法检测细胞凋亡相关蛋白的表达;检测每组细胞中过氧化氢酶(catalase,CAT)、超氧化物歧化酶(superoxide dismutase,SOD)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)、Na+K+-ATP酶活力和丙二醛(malondialdehyde,MDA)含量。结果:山楂原花青素提取物、表儿茶素和原花青素B2呈时间和质量浓度依赖性地显著抑制SMMC-7721细胞的增殖(P<0.05),促进细胞凋亡;与对照组相比,SMMC-7721细胞中SOD、CAT、GSH-Px、Na+K+-ATP酶活力降低,MDA含量升高;细胞凋亡相关蛋白半胱天冬酶-8、半胱天冬酶-3、Bcl-2相关X蛋白表达量和多聚二磷酸腺苷核糖聚合酶片段化增加,Bcl-2表达量降低。结论:山楂原花青素可通过影响抗氧化酶活力和细胞凋亡相关蛋白来抑制SMMC-7721细胞增殖,促进细胞凋亡。

关 键 词:山楂原花青素  抗氧化活性  人肝癌SMMC-7721细胞  细胞增殖  细胞凋亡  

Effect of Hawthorn Proanthocyanidins on Proliferation and Apoptosis of Human Hepatocellular Carcinoma SMMC-7721 Cells
SUN Siming,XU Hongwei,GUO Kaiyuan,GUO Mengran,CUI Shengnan,CUI Tong,TAN Jianxin.Effect of Hawthorn Proanthocyanidins on Proliferation and Apoptosis of Human Hepatocellular Carcinoma SMMC-7721 Cells[J].Food Science,2019,40(5):189-196.
Authors:SUN Siming  XU Hongwei  GUO Kaiyuan  GUO Mengran  CUI Shengnan  CUI Tong  TAN Jianxin
Affiliation:Engineering Research Center of Hebei Province for Agricultural Products Processing, College of Food Science and Technology, Hebei Agricultural University, Baoding 071001, China
Abstract:Objective: To investigate the effect of hawthorn proanthocyanidins extract, epicatechin and proanthocyanidin B2 on the proliferation and apoptosis of human hepatocellular carcinoma SMMC-7721 cells. Methods: SMMC-7721 cells were cultured in vitro. The effect of different concentrations of hawthorn proanthocyanidins on cell proliferation and apoptosis was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide assay and 4’,6-diamidino-2-phenylindole (DAPI) staining, respectively. The expression of apoptosis-related proteins was detected by Western blotting. The activities of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and Na+K+-ATPase and malondialdehyde (MDA) level in cells from each group were determined. Results: Hawthorn proanthocyanidins extract, epicatechin and proanthocyanidin B2 all significantly inhibited the proliferation of SMMC-7721 cells in a time-dependent and concentrationdependent manner (P < 0.05) and induced cell apoptosis. Compared with the control group, hawthorn proanthocyanidins extract, epicatechin and proanthocyanidin B2 decreased the activity of SOD, CAT, GSH-Px and Na+K+-ATPase and increased the level of MDA in SMMC-7721 cells. The expression of apoptosis-related proteins casepase-8, caspase-3, Bcl-2-associated X protein and the fragment of poly (ADP-ribose) polymerase were increased, while the expression of Bcl-2 was decreased. Conclusion: Hawthorn proanthocyanidins can inhibit the proliferation of SMMC-7721 cells and induce apoptosis through regulating antioxidant activity and apoptosis-related proteins.
Keywords:hawthorn proanthocyanidins  antioxidant activity  human hepatocellular carcinoma SMMC-7721 cells  cell proliferation  cell apoptosis  
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