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首页> 外文期刊>Cellular Physiology and Biochemistry >Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy
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Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy

机译:抗血管内皮生长因子通过调节一氧化氮释放和自噬保护视网膜色素上皮细胞免于氧化。

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>Background/Aims: the anti-vascular endothelial growth factors (VEGF), Aflibercept and Ranibizumab, are used for the treatment of macular degeneration. Here we examined the involvement of nitric oxide (NO), mitochondria function and of apoptosis/autophagy in their antioxidant effects in human retinal pigment epithelium cells (RPE). Methods: RPE were exposed to Ranibizumab/Aflibercept in the absence or presence of NO synthase (NOS) inhibitor and of autophagy activator/blocker, rapamicyn/3-methyladenine. Specific kits were used for cell viability, NO and reactive oxygen species detection and mitochondrial membrane potential measurement, whereas Western Blot was performed for apoptosis/ autophagy markers and other kinases detection. Results: In RPE cultured in physiological conditions, Aflibercept/Ranibizumab increased NO release in a dose and time-dependent way. Opposite results were obtained in RPE pretreated with hydrogen peroxide. Moreover, both the anti-VEGF agents were able to prevent the fall of cell viability and of mitochondrial membrane potential. Those effects were reduced by the NOS inhibitor and 3-methyladenine and were potentiated by rapamycin. Finally, Aflibercept and Ranibizumab counteracted the changes of apoptosis/autophagy markers, NOS, Phosphatidylinositol-3-Kinase/Protein Kinase B and Extracellular signal-regulated kinases 1/2 caused by peroxidation. Conclusion: Aflibercept and Ranibizumab protect RPE against peroxidation through the modulation of NO release, apoptosis and autophagy.
机译:> 背景/目的: 抗血管内皮生长因子(Aflibercept和Ranibizumab)用于治疗黄斑变性。在这里,我们检查了一氧化氮(NO),线粒体功能和细胞凋亡/自噬在人类视网膜色素上皮细胞(RPE)中的抗氧化作用。 方法: 在不存在或不存在NO合酶(NOS)抑制剂和自噬活化剂/阻断剂雷帕霉素/ 3-甲基腺嘌呤的情况下,将RPE暴露于Ranibizumab / Aflibercept。使用特定的试剂盒检测细胞活力,检测NO和活性氧以及检测线粒体膜电位,而使用Western Blot检测凋亡/自噬标记和其他激酶。 结果: 在生理条件下培养的RPE中,Aflibercept / Ranibizumab以剂量和时间依赖性方式增加NO的释放。在用过氧化氢预处理的RPE中获得了相反的结果。而且,两种抗VEGF剂均能够防止细胞活力和线粒体膜电位的下降。那些作用被NOS抑制剂和3-甲基腺嘌呤所减弱,而雷帕霉素则被增强。最后,Aflibercept和Ranibizumab抵消了由过氧化引起的凋亡/自噬标志物,NOS,磷脂酰肌醇-3-激酶/蛋白激酶B和细胞外信号调节激酶1/2的变化。 结论: Aflibercept和Ranibizumab通过调节NO释放,凋亡和自噬来保护RPE免受过氧化。

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