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Effects of Hindlimb Unweighting on MBP and GDNF Expression and Morphology in Rat Dorsal Root Ganglia Neurons

机译:后肢失重对大鼠背根神经节神经元MBP和GDNF表达及形态的影响

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With the development of technology and space exploration, studies on long-duration space flights have shown that microgravity induces damage to multiple organs, including the dorsal root ganglia (DRG). However, very little is known about the effects of long-term microgravity on DRG neurons. This study investigated the effects of microgravity on lumbar 5 (L5) DRG neurons in rats using the hindlimb unweighting (HU) model. Male (M) and female (F) Sprague-Dawley rats were randomly divided into M- and F-control (CON) groups and M- and F-HU groups, respectively (n = 10). At the end of HU treatment for 4 weeks, morphological changes were detected. Myelin basic protein (MBP) and degenerated myelin basic protein (dgen-MBP) expressions were analyzed by immunofluorescence and western blot assays. Glial cell line-derived neurotrophic factor (GDNF) protein and mRNA expressions were also analyzed by immunohistochemistry, western blot, and RT-PCR analysis, respectively. Compared with the corresponding CON groups, the HU groups exhibited slightly loose junctions between DRG neurons, some separated ganglion cells and satellite cells, and lightly stained Nissl bodies that were of smaller size and had a scattered distribution. High levels of dgen-MBP and low MBP expressions were appeared and GDNF expressions were significantly decreased in both HU groups. Changes were more pronounced in the F-HU group than in the M-HU group. In conclusion, HU treatment induced damage of L5 DRG neurons, which was correlated with decreased total MBP protein expression, increased dgen-MBP expression, and reduced GDNF protein and mRNA expression. Importantly, these changes were more severe in F-HU rats compared with M-HU rats.
机译:随着技术和太空探索的发展,对长时间太空飞行的研究表明,微重力对包括背根神经节(DRG)在内的多个器官造成损害。然而,关于长期微重力对DRG神经元的影响知之甚少。这项研究使用后肢解脱(HU)模型研究了微重力对大鼠腰5(L5)DRG神经元的影响。将雄性(M)和雌性(F)Sprague-Dawley大鼠随机分为M-和F-control(CON)组以及M-和F-HU组(n = 10)。 HU治疗结束4周后,检测到形态变化。髓磷脂碱性蛋白(MBP)和变性髓鞘碱性蛋白(dgen-MBP)的表达通过免疫荧光和蛋白质印迹分析进行了分析。胶质细胞源性神经营养因子(GDNF)蛋白和mRNA表达也分别通过免疫组织化学,免疫印迹和RT-PCR分析。与相应的CON组相比,HU组在DRG神经元之间,一些分离的神经节细胞和卫星细胞之间表现出稍微松散的连接,并且具有较小的尺寸和分散的轻度染色的尼氏体。在两个HU组中均出现了高水平的dgen-MBP和低水平的MBP表达,而GDNF表达则明显降低。与M-HU组相比,F-HU组的变化更为明显。总之,HU治疗诱导了L5 DRG神经元的损伤,这与总MBP蛋白表达降低,dgen-MBP表达升高以及GDNF蛋白和mRNA表达降低有关。重要的是,与M-HU大鼠相比,这些变化在F-HU大鼠中更为严重。

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