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国家自然科学基金(81000383)

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αB-crystallin malondialdehyde,superoxide dismutase, and lutathione peroxidase changes in X-ray irradiated rat lens被引量:1
2011年
AIM: To evaluate αB-crystallin malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPx) changes in X-ray irradiated rat lens. METHODS: Eight-week-old Sprague-Dawley male rats received X-ray irradiation to the head with rest of the body protected. The exposure dose ranged from 2 to 25 Grays (Gy). The cataract status were examined by slit lamp and rated with 'four-grade systems' post-irradiation. The lens MDA level, and the activities of SOD and GPx were measured in a short-term experiment post-irradiation, and αB-crystallin protein levels were quantified. RESULTS: The lenses of normal control and the X-ray irradiated groups with the dose up to 10 Gy remained transparent throughout the experiment. The lens first appeared tiny scatters, and even lamellar opacities in the posterior capsule 45 days post-irradiation with the dose of 15 Gy, and progressed slowly to the advance stage of cataract; while, for the higher dose (25 Gy), the opacity of lens appeared much earlier, and progressed more rapidly to mature stage of cataract within 1 month. At the end of the observation (90 days post-irradiation), almost all lenses became complete opacity with the higher dose (25 Gy). The degree of lens opacity was rated accordingly. The lens MDA level was increased, and SOD and GPx activities were decreased with a dose-dependent manner post-irradiation. The αB-crystallin protein level was decreased dose-dependently at the end point of observation. CONCLUSION: Oxidative events and αB-crystallin may play important roles in the pathogenesis of cataract in X-ray irradiated rat lens.
Guo-Xu Xu,Guo-Tong Xu
关键词:CATARACT
人源促红细胞生成素在Mller细胞中拮抗谷氨酸毒性作用的研究
2013年
目的观察高浓度谷氨酸刺激条件下Muller细胞的变化以及促红细胞生成素(erythropoietin,EPO)的保护作用是否与维持Muller细胞的谷氨酸转运功能相关。方法用MTT法检测不同浓度谷氨酸处理大鼠原代视网膜Muller细胞和大鼠视网膜Muller细胞系rMC-1所引起的细胞活力变化。选择能显著降低细胞活力的最低谷氨酸剂量建立细胞损伤模型,并研究不同浓度EPO干预后细胞活力的变化。TUNEL(terminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling)法检测各组细胞凋亡情况,Western印迹法检测谷氨酸转运体GLSAT在蛋白水平的变化。结果无论是在原代大鼠Muller细胞还是rMC-1细胞系中,谷氨酸的细胞毒性作用均呈剂量依赖趋势。原代Muller细胞中,12 mmol/L谷氨酸使细胞活力降低15.5%,10 mmol/L谷氨酸使rMC-1细胞活力降低15.6%;此时细胞凋亡明显增加,GLAST表达降低。0.2 U/ml和0.5 U/ml EPO分别对原代Muller细胞和rMC-1细胞的保护作用最佳,细胞凋亡数量显著减少,并防止了GLAST蛋白水平的降低。结论体外高浓度谷氨酸可损伤Muller细胞,EPO可以通过维持谷氨酸转运体GLAST水平等机制维持Muller对谷氨酸的正常摄取、抑制凋亡发生。
雇利敏张敬法徐华吕立夏李维业徐国彤
关键词:促红细胞生成素谷氨酸谷氨酸转运体
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