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首页> 外文期刊>Neurochemistry International: The International Journal for the Rapid Publication of Critical Reviews, Preliminary and Original Research Communications in Neurochemistry >Serum deprivation inhibits glutathione depletion-induced death in embryonic cortical neurons: evidence against oxidative stress as a final common mediator of neuronal apoptosis.
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Serum deprivation inhibits glutathione depletion-induced death in embryonic cortical neurons: evidence against oxidative stress as a final common mediator of neuronal apoptosis.

机译:血清剥夺抑制了谷胱甘肽耗竭诱导的胚胎皮质神经元死亡:抗氧化应激作为神经元凋亡的最终常见介质的证据。

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We have previously shown that glutamate-induced cystine deprivation of embryonic cortical neurons leads to intracellular depletion of the antioxidant glutathione, consequent oxidative stress and apoptotic cell death. To test the hypothesis that glutathione depletion and oxidative stress represent a common pathway of neuronal apoptosis, we examined the effect of a variety of antioxidants on serum deprivation-induced death in embryonic cortical neurons. A host of antioxidant agents, capable of abrogating glutathione depletion-induced apoptosis in cortical neurons, were unable to inhibit serum deprivation-induced death in these cells. To test whether serum deprivation and glutathione depletion involve different or antagonistic pathways, we serum-deprived cortical neurons at the time of induction of glutathione depletion. Surprisingly, we found that serum deprivation diminished glutathione depletion-induced death as compared to cultures treated with growth factors or serum. These observations suggest that serum deprivation antagonizes the cell death signaling pathway activated by glutathione depletion and that serum and growth factors can enhance susceptibility to oxidative stress. Consistent with these conclusions, we show that growth factors or serum added in combination with antioxidants possess superior survival promoting effects as compared to either agent alone.
机译:先前我们已经表明,谷氨酸诱导的胚胎皮质神经元的胱氨酸剥夺会导致抗氧化剂谷胱甘肽的细胞内消耗,随后的氧化应激和凋亡细胞死亡。为了检验谷胱甘肽耗竭和氧化应激代表神经元凋亡的常见途径的假说,我们检查了多种抗氧化剂对血清剥夺诱导的胚胎皮质神经元死亡的影响。能够消除谷胱甘肽耗竭诱导的皮质神经元凋亡的许多抗氧化剂无法抑制这些细胞中血清耗竭诱导的死亡。为了测试血清剥夺和谷胱甘肽耗竭是否涉及不同或拮抗途径,我们在诱导谷胱甘肽耗竭时血清剥夺了皮质神经元。令人惊讶地,我们发现与用生长因子或血清处理的培养物相比,血清剥夺减少了谷胱甘肽耗竭诱导的死亡。这些观察结果表明,血清剥夺拮抗由谷胱甘肽消耗激活的细胞死亡信号通路,血清和生长因子可以增强对氧化应激的敏感性。与这些结论一致,我们表明与单独使用任何一种药物相比,与抗氧化剂结合使用的生长因子或血清均具有优异的存活促进作用。

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