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首页> 外文期刊>Neuropeptides: An International Journal >FNDC5 expression in Purkinje neurons of adult male rats with acute spinal cord injury following treatment with methylprednisolone
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FNDC5 expression in Purkinje neurons of adult male rats with acute spinal cord injury following treatment with methylprednisolone

机译:用甲基己酮治疗后成人雄性大鼠Purkinje神经元的FNDC5表达急性脊髓损伤

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Spinal cord injury (SCI) is a serious and complex medical condition that can happen to anyone. At present, therapy mainly focuses on rehabilitation and pharmacological treatment, such as methylprednisolone (MP). Supra-spinal changes in certain structures, such as the cerebellum, that receive many afferents from the spinal cord might be one reason for unsuccessful therapeutic outcomes. Recently, the expression of FNDC5 was reported in cerebellar Purkinje cells as a possible neuroprotective agent. In the present study, we considered the expression of FNDC5 in Purkinje cells following SCI with and without MP administration in adult rats with SCI. Thirty-five adult male rats were used in this study. The animals were randomly allocated into five groups, including SCI, spinal cord injury with methylprednisolone treatment (SCI + MP), operation sham, control, and operation sham with MP. Induction of SCI was achieved by using special clips to compress the spinal cord at a determined level. After a certain interval time, the animals underwent study for FNDC5 expression, apoptosis by using immunohistochemistry, Western blotting, and TUNEL and Nissl staining. Our results showed a significant decrease in the number of Purkinje cells following SCI. Therapy with MP inhibits apoptosis in irFNDC5 Purkinje cells and restores them. Expression of FNDC5 significantly increased in SCI and decreased following MP therapy. We also showed other cerebellar cells with FNDC5 immunoreactivity in the two other cerebellar layers that were firstly reported. Since irisin is known as a plasma product of FNDC5, we think it might be a plasma marker following therapeutic efforts for SCI; however, it needs further research. In addition, it is possible that changes in FNDC5 expression in Purkinje cells might be related to neurogenesis in the cerebellum with unknown mechanisms.
机译:脊髓损伤(SCI)是一个严重而复杂的医疗条件,可能发生在任何人身上。目前,疗法主要侧重于康复和药理治疗,例如甲基己酮(MP)。从脊髓接受许多患有许多引起的细胞的某些结构中的Supra-Spinal变化可能是不成功治疗结果的一个原因。最近,将FNDC5的表达在小脑purkinje细胞中报告为可能的神经保护剂。在本研究中,我们考虑了在SCI和没有SCI的成年大鼠中的SCI和没有MP给药后的Purkinje细胞中FNDC5的表达。本研究使用了三十五只成年雄性大鼠。将这些动物随机分配到五组中,包括SCI,脊髓损伤与甲基己酮龙治疗(SCI + MP),操作假,控制和操作MP。通过使用特殊夹子在确定的水平下压缩脊髓来实现SCI的诱导。经过一定的间隔时间,通过使用免疫组织化学,蛋白质印迹和TUNEL和NISSL染色来完成一定间隔时间。我们的结果表明,SCI后的Purkinje细胞数量显着降低。患有MP的治疗抑制IRFNDC5 Purkinje细胞中的细胞凋亡并恢复它们。 SCI中FNDC5的表达显着增加,MP疗法下降减少。我们还在首先报道的另外两个小脑层中显示出具有FNDC5免疫反应性的其他小脑细胞。由于IRISIN被称为FNDC5的血浆产物,因此我们认为这可能是SCI治疗努力后的等离子体标记;但是,它需要进一步研究。此外,Purkinje细胞中FNDC5表达的变化可能与小脑中的神经发生有关,具有未知的机制。

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