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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-硝基脲通过抑制NF-B活化诱导大鼠的视网膜变性

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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:视网膜炎Pigmentosa(RP)是一组遗传性神经变性疾病,其特征是通过凋亡丧失光感受器细胞的损失。 N-甲基-N-硝基脲(MNU)是一种烷基化毒物,其诱导感光体细胞死亡类似于遗传性RP。本研究旨在探讨核因子B(NF-B)在MNU诱导的光感受器变性中的作用。成人大鼠接受了单一的腹膜内注射MNU(60mg / kg体重)。苏木精和曙红染色在MNU治疗后展示了逐步的外核层(ONL)丧失。透射电子显微镜显示核细胞,在感光体中的染色质谱,慢性溶酶体增加,和乳菌状的大鼠中的裂解的视网膜着色上皮细胞。 ONL中的许多光感受体细胞显示出阳性TUNEL染色和凋亡率在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出ONL变薄和脉络膜厚度降低。 ElectroreTinoGro表示降低了在施力条件下占据的波幅。 Western印迹分析表明,核IB水平的增加,而核NF-B P65在MNU处理的大鼠的视网膜中显着下降。这些发现表明MNU导致选择性感光体降解,这与NF-B活化的抑制相关。

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