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N-methyl-N-nitrosourea induces retinal degeneration in the rat via the inhibition of NF-B activation

机译:N-甲基-N-亚硝基脲通过抑制NF-B激活而诱导大鼠视网膜变性

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摘要

Retinitis pigmentosa (RP) is a group of inherited neurodegenerative diseases characterized by the loss of photoreceptor cells through apoptosis. N-methyl-N-nitrosourea (MNU) is an alkylating toxicant that induces photoreceptor cell death resembling hereditary RP. This study aimed to investigate the role of nuclear factor B (NF-B) in MNU-induced photoreceptor degeneration. Adult rats received a single intraperitoneal injection of MNU (60mg/kg bodyweight). Hematoxylin and eosin staining demonstrated progressive outer nuclear layer (ONL) loss after MNU treatment. Transmission electron microscopy revealed nuclear pyknosis, chromatin margination in the photoreceptors, increased secondary lysosomes, and lobulated retinal-pigmented epithelial cells in MNU-treated rats. Numerous photoreceptor cells in the ONL showed positive TUNEL staining and apoptosis rate peaked at 24hours. Enhanced depth imaging spectral-domain optical coherence tomography showed ONL thinning and decreased choroid thickness. Electroretinograms showed decreased A wave amplitude that predominated in scotopic conditions. Western blot analysis showed that nuclear IB level increased, whereas nuclear NF-B p65 decreased significantly in the retinas of MNU-treated rats. These findings indicate that MNU leads to selective photoreceptor degradation, and this is associated with the inhibition of NF-B activation.
机译:色素性视网膜炎(RP)是一组遗传性神经退行性疾病,其特征是通过凋亡使感光细胞丧失。 N-甲基-N-亚硝基脲(MNU)是一种烷基化有毒物质,可诱发类似于遗传性RP的感光细胞死亡。这项研究旨在调查核因子B(NF-B)在MNU诱导的感光细胞变性中的作用。成年大鼠腹膜内注射MNU(60mg / kg体重)。苏木精和曙红染色显示MNU治疗后进行性外核层(ONL)丢失。透射电子显微镜显示在MNU治疗的大鼠中核固缩,光感受器的染色质边缘化,次级溶酶体增加以及视网膜色素上皮细胞小叶化。 ONL中的许多感光细胞显示出阳性的TUNEL染色,并且凋亡率在24小时达到峰值。增强的深度成像光谱域光学相干断层扫描显示ONL变薄,脉络膜厚度减小。视网膜电图显示在暗视条件下占主导地位的A波振幅降低。蛋白质印迹分析表明,在用MNU处理的大鼠的视网膜中,核IB水平升高,而核NF-B p65显着下降。这些发现表明,MNU导致选择性的感光细胞降解,这与抑制NF-B激活有关。

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