首页> 美国卫生研究院文献>International Journal of Molecular Sciences >α-Tocopherol at Nanomolar Concentration Protects PC12 Cells from Hydrogen Peroxide-Induced Death and Modulates Protein Kinase Activities
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α-Tocopherol at Nanomolar Concentration Protects PC12 Cells from Hydrogen Peroxide-Induced Death and Modulates Protein Kinase Activities

机译:纳摩尔浓度的α-生育酚可保护PC12细胞免受过氧化氢诱导的死亡并调节蛋白激酶活性

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摘要

The aim of this work was to compare protective and anti-apoptotic effects of α-tocopherol at nanomolar and micromolar concentrations against 0.2 mM H2O2-induced toxicity in the PC12 neuronal cell line and to reveal protein kinases that contribute to α-tocopherol protective action. The protection by 100 nM α-tocopherol against H2O2-induced PC12 cell death was pronounced if the time of pre-incubation with α-tocopherol was 3–18 h. For the first time, the protective effect of α-tocopherol was shown to depend on its concentration in the nanomolar range (1 nM < 10 nM < 100 nM), if the pre-incubation time was 18 h. Nanomolar and micromolar α-tocopherol decreased the number of PC12 cells in late apoptosis induced by H2O2 to the same extent if pre-incubation time was 18 h. Immunoblotting data showed that α-tocopherol markedly diminished the time of maximal activation of extracellular signal-regulated kinase 1/2 (ERK 1/2) and protein kinase B (Akt)-induced in PC12 cells by H2O2. Inhibitors of MEK 1/2, PI 3-kinase and protein kinase C (PKC) diminished the protective effect of α-tocopherol against H2O2-initiated toxicity if the pre-incubation time was long. The modulation of ERK 1/2, Akt and PKC activities appears to participate in the protection by α-tocopherol against H2O2-induced death of PC12 cells. The data obtained suggest that inhibition by α-tocopherol in late stage ERK 1/2 and Akt activation induced by H2O2 in PC12 cells makes contribution to its protective effect, while total inhibition of these enzymes is not protective.
机译:这项工作的目的是比较在纳摩尔和微摩尔浓度下α-生育酚对PC12神经元细胞系中0.2 mM H2O2诱导的毒性的保护和抗凋亡作用,并揭示有助于α-生育酚保护作用的蛋白激酶。如果与α-生育酚的预温育时间为3–18 h,则100 nMα-生育酚对H2O2诱导的PC12细胞死亡的保护作用显着。如果预孵育时间为18 h,则首次显示α-生育酚的保护作用取决于其在纳摩尔浓度(1 nM <10 nM <100 nM)中的浓度。如果预孵育时间为18 h,则纳摩尔和微摩尔α-生育酚在H2O2诱导的晚期凋亡中减少了PC12细胞的数量。免疫印迹数据表明,α-生育酚显着减少了H2O2诱导PC12细胞中细胞外信号调节激酶1/2(ERK 1/2)和蛋白激酶B(Akt)的最大活化时间。如果预孵育时间长,MEK 1/2,PI 3-激酶和蛋白激酶C(PKC)的抑制剂会减弱α-生育酚对H2O2引发的毒性的保护作用。 ERK 1/2,Akt和PKC活性的调节似乎参与了α-生育酚对H2O2诱导PC12细胞死亡的保护作用。获得的数据表明,在PC12细胞中,α-生育酚在晚期ERK 1/2的抑制和H2O2诱导的PC12细胞的Akt激活对其保护作用有所贡献,而对这些酶的完全抑制则无保护作用。

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