首页> 外文期刊>Endothelium: Journal of endothelial cell research >Effects of novel safrole oxide derivatives, 1-propyl-3-(3,4-methylenedioxyphenyl)-2-propanol and 1-isopropoxy-3-(3,4-methylenedioxyphenyl)-2-propanol, on apoptosis induced by deprivation of survival factors in vascular endothelial cells.
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Effects of novel safrole oxide derivatives, 1-propyl-3-(3,4-methylenedioxyphenyl)-2-propanol and 1-isopropoxy-3-(3,4-methylenedioxyphenyl)-2-propanol, on apoptosis induced by deprivation of survival factors in vascular endothelial cells.

机译:新型黄樟脑氧化物衍生物1-丙基-3-(3,4-亚甲基二氧苯基)-2-丙醇和1-异丙氧基-3-(3,4-亚甲基二氧苯基)-2-丙醇对存活剥夺诱导的细胞凋亡的影响血管内皮细胞中的因子。

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摘要

Two safrole oxide derivatives, 1-propoxy-3-(3,4-methylenedioxyphenyl)-2-propanol (FOD) and 1-isopropoxy-3-(3,4-methylenedioxyphenyl)-2-propanol (GOD), were newly synthesized as promoters of apoptosis in vascular endothelial cells. The purpose of this study was to investigate the effects of these two safrole oxide derivatives on cell growth and apoptosis induced by deprivation of survival factors (serum and fibroblast growth factors, aFGF and bFGF) in vascular endothelial cells (VECs). MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium) method, agarose gel electrophoresis, laser scanning confocal microscopy, flow cytometry (FCM), and immunofluorescence assay were used. The cells deprived of FGF and serum were exposed to FOD or GOD 30 to 90 mg x L(-1) for 24 h, cell growth was suppressed (p < .05), whereas detachment and DNA fragmentation of these cells were promoted (p < .01). When the cells were treated with FOD 90 mg x L(-) for 24 h, apoptosis rate was 14.99% (p < .01). There were more cells inG2-M phase and less cells in S phase. At 90 mg x L(-1) concentration, GOD blocked 77.03%of the cells at G0-G1 phase., P53 level in VEC exposed to FOD or GOD was increased (p < .01). The data suggested that FOD and GOD might promote apoptosis of VEC by affect the cell cycle distribution, whereas P53 was involved in this pathway.
机译:新合成了两种黄樟脑氧化物衍生物,即1-丙氧基-3-(3,4-亚甲基二氧基苯基)-2-丙醇(FOD)和1-异丙氧基-3-(3,4-亚甲基二氧基苯基)-2-丙醇(GOD)作为血管内皮细胞凋亡的促进剂。这项研究的目的是研究这两种黄樟脑氧化物衍生物对血管内皮细胞(VEC)中存活因子(血清和成纤维细胞生长因子,aFGF和bFGF)的剥夺诱导的细胞生长和凋亡的影响。使用MTT(3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四唑鎓)方法,琼脂糖凝胶电泳,激光扫描共聚焦显微镜,流式细胞术(FCM)和免疫荧光分析。剥夺FGF和血清的细胞暴露于30至90 mg x L(-1)的FOD或GOD中24小时,细胞生长受到抑制(p <.05),而这些细胞的分离和DNA断裂得到促进(p <.01)。当将细胞用90 mg x L(-)FOD处理24 h时,细胞凋亡率为14.99%(p <.01)。 G2-M期细胞较多,S期细胞较少。在90 mg x L(-1)浓度下,GOD在G0-G1期阻断了77.03%的细胞,暴露于FOD或GOD的VEC中的P53水平升高(p <.01)。数据表明,FOD和GOD可能通过影响细胞周期分布来促进VEC的凋亡,而P53参与了该途径。

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