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Effects of Light Exposure and Use of Intraocular Lens on Retinal Pigment Epithelial Cells In Vitro

机译:光照和人工晶状体对视网膜色素上皮细胞体外的影响

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摘要

To investigate the effect of a blue light-filtering intraocular lens (IOL) and a UV-absorbing IOL on light-induced damage to retinal pigment epithelial (RPE) cells laden with the lipofuscin fluorophore N-retinylidene-N-retinylethanolamine (A2E), A2E-laden RPE cells were exposed to white light which was filtered by either a blue light-filtering IOL or a UV-absorbing IOL. After 30 min of illumination the cell viability and the level of reactive oxygen species (ROS), free glutathione (GSH), vascular endothelial growth factor (VEGF) and pigment epithelium-derived factor (PEDF) were determined. In the absence of an IOL, the white light exposure decreased cell viability to 37.2% of the nonirradiated control. The UV-absorbing IOL tended to reduce light-induced cell death; however, the decrease was not significant. The blue light-filtering IOL significantly attenuated light-induced cell damage, increasing cell viability to 79.5% of the nonirradiated control. The presence of the blue light-filtering IOL significantly increased GSH and PEDF levels, and decreased ROS and VEGF levels. This study suggests that a blue light-filtering IOL may be more protective against A2E-induced light damage and inhibit more light-induced ROS and VEGF production than a conventional UV-absorbing IOL. [PUBLICATION ABSTRACT]
机译:要研究滤蓝光的人工晶状体(IOL)和吸收紫外线的IOL对光诱导的对充满脂褐素荧光团N-视黄叉基-N-视黄基乙醇胺(A2E)的视网膜色素上皮(RPE)细胞的损伤的影响,将载有A2E的RPE细胞暴露于白光,该白光通过滤蓝光的IOL或吸收紫外线的IOL过滤。照射30分钟后,测定细胞活力和活性氧(ROS),游离谷胱甘肽(GSH),血管内皮生长因子(VEGF)和色素上皮衍生因子(PEDF)的水平。在没有IOL的情况下,白光暴露使细胞活力降低至未辐照对照的37.2%。吸收紫外线的IOL倾向于减少光诱导的细胞死亡。但是,下降幅度不大。滤蓝光的IOL显着减弱了光诱导的细胞损伤,将细胞活力提高至未照射对照的79.5%。滤蓝光的IOL的存在显着增加了GSH和PEDF的水平,并降低了ROS和VEGF的水平。这项研究表明,与传统的吸收紫外线的IOL相比,过滤蓝光的IOL可能更能抵抗A2E引起的光损伤,并抑制更多的光引起的ROS和VEGF的产生。 [出版物摘要]

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    《Photochemistry and Photobiology》 |2009年第4期|p.966-969|共4页
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    Sheng Hui1, Lu Yi*1 and Qing L. Fengling21 Department of Ophthalmology, Eye & ENT Hospital of Fudan University, Shanghai, China2 Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry,Chinese Academy of Science, Shanghai, ChinaReceived 19 May 2008, accepted 14 October 2008, DOI:10.1111/j.1751-1097.2008.00506.x* Corresponding author email: luyi_cent@yahoo.com.cn (Lu Yi)© 2009 The Authors. Journal Compilation. The American Society of Photobiology 0031-8655/09;

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