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Effect of safrole oxide on vascular endothelial cell growth and apoptosis induced by deprivation of fibroblast growth factor

机译:氧化丙烯酰胺对剥夺成纤维细胞生长因子诱导的血管内皮细胞生长和凋亡的影响

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摘要

AIM: To investigate effect of safrole oxide on cell growth and apoptosis induced by deprivation of survival factors (fibroblast growth factors, aFGF and bFGF) in vascular endothelial cells (VEC). METHODS: Morphological changes were observed by light microscopy. Cell growth was determined by MTT (3-[4, 5-dimethyl thiazol-2-yl]-2, 5-diphenyltetrazolium) method. DNA fragmentation was analyzed by agarose gel electrophoresis and fluorescence microscopy. Cell cycle distribution was analyzed by flow cytometry (FCM). RESULTS: The cells deprived of FGF were exposed to safrole oxide 5 -25 mg/L for 24 h. Cells spreading and growth were promoted (P < 0.01), detachment and DNA fragmentation of these cells were suppressed (P < 0.01), safrole oxide 10 mg/L had no obvious effect on cell cycle distribution ( P > 0.05). When the cells were treated with safrole oxide 50 -100 mg/L, detachment and DNA fragmentation of VEC were promoted (P < 0.01). The cell cycle was blocked at G_2-M phase by safrole oxide 100 mg/L. CONCLUSION: Safrole oxide 10 mg/L inhibited, but 100 mg/L promoted apoptosis of VEC. Safrole oxide might be an important compound that affects VEC growth and apoptosis.
机译:目的:研究黄樟脑氧化物对血管内皮细胞(VEC)中存活因子(成纤维细胞生长因子,aFGF和bFGF)被剥夺诱导的细胞生长和凋亡的影响。方法:通过光学显微镜观察形态变化。细胞生长通过MTT(3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四唑)方法测定。通过琼脂糖凝胶电泳和荧光显微镜分析DNA片段化。通过流式细胞术(FCM)分析细胞周期分布。结果:剥夺FGF的细胞暴露于5 -25 mg / L的黄樟脑氧化物24 h。促进了细胞的扩散和生长(P <0.01),抑制了这些细胞的脱离和DNA断裂(P <0.01),氧化黄樟醇10 mg / L对细胞周期分布没有明显影响(P> 0.05)。当用50 -100 mg / L的黄樟脑氧化物处理细胞时,促进了VEC的分离和DNA断裂(P <0.01)。细胞周期在G_2-M相被黄樟醇100 mg / L阻断。结论:黄樟脑氧化物可抑制10 mg / L,而100 mg / L可促进VEC的凋亡。氧化黄樟脑可能是影响VEC生长和凋亡的重要化合物。

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