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首页> 外文期刊>Investigative ophthalmology & visual science >Evaluation of Oxidative Stress Markers in Human Conjunctival Epithelial Cells Exposed to Diesel Exhaust Particles (DEP)
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Evaluation of Oxidative Stress Markers in Human Conjunctival Epithelial Cells Exposed to Diesel Exhaust Particles (DEP)

机译:评价人结膜上皮细胞暴露于柴油机排气颗粒(DEP)的氧化应激标记

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Purpose: The aim of this study was to evaluate oxidative stress markers in human conjunctival epithelial cells (IOBA-NHC) exposed to diesel exhaust particles (DEP). Methods: Reactive oxygen (ROS) and nitrogen (RNS) species production; hydrogen peroxide (H2O2) levels; protein oxidation; antioxidant enzymes activities (superoxide dismutase [SOD], catalase [CAT], glutathione peroxidase [GPx], glutathione S-transferase [GST], and glutathione reductase [GR]); total reactive antioxidant potential (TRAP); reduced (GSH) and oxidized glutathione (GSSG) were evaluated. Transmission electron microscopy was performed to evaluate DEP uptake. Results: Diesel exhaust particles were entrapped by membrane protrusions developed by IOBA-NHC. Cells exposed to DEP 50 and 100 ??g/mL showed a significant increase in ROS, RNS, H2O2 levels, SOD, GPx, and GST compared with the control group. A significant decay in GR was observed in both groups, meanwhile CAT levels remained unchanged. The group exposed to DEP 100 ??g/mL displayed a significant increase in protein oxidation. In both groups, TRAP was significantly reduced as well as the GSH/GSSG ratio. Conclusions: The decrease in nonenzymatic antioxidants and the compensatory increase of SOD, GPX, and GST activities are consequence of the increase in ROS and RNS production due to DEP exposure and its accumulation inside the cells. The decay in GR activity leads to the decrease in GSH/GSSG recycling. These results suggest that oxidative stress could play an important role in the development of DEP effects on human conjunctival epithelial cells.
机译:目的:本研究的目的是评估暴露于柴油机排气颗粒(DEP)的人结膜上皮细胞(IOBA-NHC)中的氧化应激标记。方法:生产活性氧(ROS)和氮(RNS);过氧化氢(H2O2)含量;蛋白质氧化;抗氧化酶活性(超氧化物歧化酶[SOD],过氧化氢酶[CAT],谷胱甘肽过氧化物酶[GPx],谷胱甘肽S-转移酶[GST]和谷胱甘肽还原酶[GR]);总活性抗氧化剂电位(TRAP);还原(GSH)和氧化型谷胱甘肽(GSSG)进行了评估。进行透射电子显微镜以评估DEP摄取。结果:柴油机排气颗粒被IOBA-NHC形成的膜突出物截留。与对照组相比,暴露于DEP 50和100μg/ mL的细胞显示ROS,RNS,H2O2水平,SOD,GPx和GST显着增加。两组均观察到GR显着下降,同时CAT水平保持不变。暴露于DEP 100μg/ mL的组显示出蛋白质氧化的显着增加。在两组中,TRAP以及GSH / GSSG比率均显着降低。结论:非酶类抗氧化剂的减少以及SOD,GPX和GST活性的补偿性增加是由于DEP暴露及其在细胞内积累引起的ROS和RNS生成增加的结果。 GR活性下降导致GSH / GSSG循环利用减少。这些结果表明,氧化应激可能在DEP对人结膜上皮细胞的作用发展中起重要作用。

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