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首页> 外文期刊>International journal of molecular medicine >Protective effect of 7-difluoromethoxy-5,4'-Di-hydroxyl isoflavone against the damage induced by glutamate in PC12 cells
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Protective effect of 7-difluoromethoxy-5,4'-Di-hydroxyl isoflavone against the damage induced by glutamate in PC12 cells

机译:7-二氟甲氧基-5,4'-二羟基异黄酮对PC12细胞谷氨酸诱导的损伤的保护作用

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7-difluoromethoxy-5,4'-Di-hydroxyl isoflavone (dFGEN), prepared by the difluoromethylation of genistein, is an active chemical entity. In this study, our main purpose was to investigate whether dFGEN had an effect on glutamate-induced apoptosis in cultured PC12 cells. The PC12 cells were treated with different glutamate concentrations for 24 h in vitro. The PC12 cells impaired by glutamate were used as the cell model of excitability. Cells were incubated for 30 min with genistein, dFGEN, vitamin E, and exposed to 10 mM glutamate for 24 h. Cell morphology was observed by light microscopy. The growth and proliferation of PC12 cells were detected by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay. Cell apoptosis was determined by flow cytome-try (FCM) with propidium iodide (PI) staining. The activity of lactate dehydrogenase (LDH), superoxide dismutase (SOD) and the content of malondialdelyde (MDA) were measured by kits, respectively. Acridine orange (AO) staining was used to detect characteristics of cell apoptosis. When PC12 cells were incubated with glutamate for 24 h, cells appeared to have significant changes in shape. The cellular viability was reduced and the apoptotic rate was increased. The levels of LDH and the content of MDA were increased. The activity of SOD was decreased. After PC12 cells were pretreated with dFGEN, dFGEN significantly improved cell morphology, cell growth and proliferation, suppressed apoptosis of cells, reduced the release of LDH, improving SOD activity and decreased MDA content in a concentration-dependent manner. AO staining displayed that apoptosis was decreased. These results suggested that dFGEN has a protective effect against glutamate-induced damage in PC12 cells. dFGEN seemed to have a better protective effect than the lead compound genistein in a concentration-dependent manner. The mechanism of protective effect of dFGEN may be mainly related to its antioxidative activity.
机译:通过染料木黄酮的二氟甲基化制备的7-二氟甲氧基-5,4'-二羟基异黄酮(dFGEN)是一种活性化学实体。在这项研究中,我们的主要目的是研究dFGEN是否对培养的PC12细胞中谷氨酸诱导的细胞凋亡产生影响。在体外用不同的谷氨酸浓度处理PC12细胞24小时。谷氨酸损伤的PC12细胞被用作兴奋性的细胞模型。将细胞与染料木黄酮,dFGEN,维生素E孵育30分钟,然后暴露于10 mM谷氨酸盐中24小时。通过光学显微镜观察细胞形态。通过3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四氮唑溴化物(MTT)检测法检测PC12细胞的生长和增殖。细胞凋亡通过碘化丙啶(PI)染色的流式细胞仪(FCM)确定。用试剂盒分别测定乳酸脱氢酶(LDH),超氧化物歧化酶(SOD)和丙二醛(MDA)的含量。 cr啶橙(AO)染色用于检测细胞凋亡的特征。当PC12细胞与谷氨酸一起温育24小时时,细胞似乎具有明显的形状变化。细胞活力降低,细胞凋亡率增加。 LDH水平和MDA含量增加。 SOD的活性降低。 dFGEN预处理PC12细胞后,dFGEN以浓度依赖的方式显着改善细胞形态,细胞生长和增殖,抑制细胞凋亡,减少LDH的释放,改善SOD活性并降低MDA含量。 AO染色显示凋亡减少。这些结果表明,dFGEN对谷氨酸诱导的PC12细胞损伤具有保护作用。 dFGEN似乎以浓度依赖性的方式比先导化合物染料木黄酮具有更好的保护作用。 dFGEN保护作用的机制可能主要与其抗氧化活性有关。

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