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Study of Histopathological and Molecular Changes of Rat Kidney under Simulated Weightlessness and Resistance Training Protective Effect

机译:模拟失重和抵抗训练保护作用下大鼠肾脏的组织病理学和分子变化的研究

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摘要

To explore the effects of long-term weightlessness on the renal tissue, we used the two months tail suspension model to simulate microgravity and investigated the simulated microgravity on the renal morphological damages and related molecular mechanisms. The microscopic examination of tissue structure and ultrastructure was carried out for histopathological changes of renal tissue morphology. The immunohistochemistry, real-time PCR and Western blot were performed to explore the molecular mechanisms associated the observations. Hematoxylin and eosin (HE) staining showed severe pathological kidney lesions including glomerular atrophy, degeneration and necrosis of renal tubular epithelial cells in two months tail-suspended rats. Ultrastructural studies of the renal tubular epithelial cells demonstrated that basal laminas of renal tubules were rough and incrassate with mitochondria swelling and vacuolation. Cell apoptosis in kidney monitored by the expression of Bax/Bcl-2 and caspase-3 accompanied these pathological damages caused by long-term microgravity. Analysis of the HSP70 protein expression illustrated that overexpression of HSP70 might play a crucial role in inducing those pathological damages. Glucose regulated protein 78 (GRP78), one of the endoplasmic reticulum (ER) chaperones, was up-regulated significantly in the kidney of tail suspension rat, which implied that ER-stress was associated with apoptosis. Furthermore, CHOP and caspase-12 pathways were activated in ER-stress induced apoptosis. Resistance training not only reduced kidney cell apoptosis and expression of HSP70 protein, it also can attenuate the kidney impairment imposed by weightlessness. The appropriate optimization might be needed for the long term application for space exploration.
机译:为了探讨长期失重对肾脏组织的影响,我们使用了两个月的尾部悬吊模型来模拟微重力,并研究了模拟微重力对肾脏形态损害和相关分子机制的影响。进行组织结构和超微结构的显微镜检查,以检查肾脏组织形态的组织病理学变化。进行了免疫组织化学,实时PCR和Western印迹以探索与观察结果相关的分子机制。苏木精和曙红(HE)染色显示在两个月尾悬吊的大鼠中,肾脏出现了严重的病理病变,包括肾小球萎缩,肾小管上皮细胞变性和坏死。肾小管上皮细胞的超微结构研究表明,肾小管的基底层很粗糙,并充满线粒体肿胀和空泡化。通过Bax / Bcl-2和caspase-3的表达监测肾细胞凋亡伴随长期微重力引起的这些病理损伤。对HSP70蛋白表达的分析表明,HSP70的过表达可能在诱导这些病理损伤中起关键作用。葡萄糖调节蛋白78(GRP78)是内质网伴侣蛋白之一,在尾部悬吊大鼠的肾脏中显着上调,这表明ER应激与细胞凋亡有关。此外,CHO和caspase-12通路在内质网应激诱导的细胞凋亡中被激活。抵抗训练不仅可以减少肾细胞的凋亡和HSP70蛋白的表达,还可以减轻失重对肾脏的损害。对于太空探索的长期应用,可能需要适当的优化。

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