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氧化损伤导致的视网膜变性

Retinal degeneration from oxidative damage.

作者信息

Cingolani Celia, Rogers Brian, Lu Lili, Kachi Shu, Shen Jikui, Campochiaro Peter A

机构信息

Department of Ophthalmology and Department of Neuroscience, The Johns Hopkins University School of Medicine, Maumenee 719, 600 N. Wolfe Street, Baltimore, MD 21287-9277, USA.

出版信息

Free Radic Biol Med. 2006 Feb 15;40(4):660-9. doi: 10.1016/j.freeradbiomed.2005.09.032. Epub 2005 Oct 21.

DOI:10.1016/j.freeradbiomed.2005.09.032
PMID:16458197
Abstract

Paraquat, a herbicide that generates reactive oxygen species, has been used to probe the oxidative defense systems of lung. In this study, we investigated the effects of paraquat in the retina. There was no significant decline in electroretinogram (ERG) a- or b-wave amplitudes after intravitreous injection of 1 mul of 0.5 mM paraquat in C57BL/6 mice, but loss of ERG function occurred after injection of 0.75 or 1 mM paraquat. Histology in paraquat-injected eyes showed condensation of chromatin and thinning of the inner and outer nuclear layers indicating cell death, and terminal deoxynucleotidyl transferase-mediated duTP-biotinide end labeling demonstrated that one mechanism of cell death was apoptosis. Fluorescence in the retina and retinal pigmented epithelium after intraocular injection of paraquat followed by perfusion with hydroethidine indicated high levels of superoxide radicals, and oxidative damage was demonstrated by staining for acrolein and enzyme-linked immunosorbent assay for carbonyl adducts. Paraquat-induced damage to the outer nuclear layer was greater in BALB/c mice than in C57BL/6 mice, suggesting strain differences in the oxidative defense system of photoreceptors and/or other modifier genes. Intravitreous injection of paraquat provides a new model of oxidative damage-induced retinal degeneration that is likely to be useful for testing new antioxidant treatments.

摘要

百草枯是一种能产生活性氧的除草剂,已被用于探究肺部的氧化防御系统。在本研究中,我们调查了百草枯对视网膜的影响。向C57BL/6小鼠玻璃体内注射1微升0.5毫摩尔/升的百草枯后,视网膜电图(ERG)的a波或b波振幅没有显著下降,但注射0.75或1毫摩尔/升的百草枯后出现了ERG功能丧失。注射百草枯的眼睛的组织学检查显示染色质凝聚以及内核层和外核层变薄,表明细胞死亡,末端脱氧核苷酸转移酶介导的dUTP生物素末端标记表明细胞死亡的一种机制是凋亡。向眼内注射百草枯后再用氢乙锭灌注,视网膜和视网膜色素上皮中的荧光表明超氧自由基水平很高,通过丙烯醛染色和羰基加合物的酶联免疫吸附测定证明了氧化损伤。百草枯诱导的外核层损伤在BALB/c小鼠中比在C57BL/6小鼠中更严重,这表明光感受器氧化防御系统和/或其他修饰基因存在品系差异。玻璃体内注射百草枯提供了一种氧化损伤诱导的视网膜变性新模型,可能有助于测试新的抗氧化治疗方法。

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