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Neuronal loss and expression of neurotrophic factors in a model of rat chronic compressive spinal cord injury.

机译:大鼠慢性压迫性脊髓损伤模型中的神经元丢失和神经营养因子的表达。

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STUDY DESIGN: An experimental animal study about neuronal loss and the expression of neurotrophic factors in the chronic compressive spinal cords. OBJECTIVES: To investigate neuronal loss and the expression of neurotrophic factors in the chronic compressive spinal cords of rats, and to evaluate effects of decompressive procedures for the neuronal loss. SUMMARY OF BACKGROUND DATA: Chronic compression of spinal cords induces the loss of motor neurons in the anterior horn. However, the precise mechanism of this neuronal loss is not still understood completely. Furthermore, it is uncertain whether decompressive procedures prevent this neuronal loss or not. METHODS: A thin expanding polymer sheet was implanted microsurgically underneath T7 laminae of rats. After 6, 9, 12, and 15 weeks, the thoracic spinal cord was harvested and examined histopathologically. The expression of neurotrophic factors, including NGF, BDNF, NT-3, GDNF, CNTF, and VEGF, was analyzed using semiquantitative RT-PCR, enzyme immunoassay,and immunohistochemistry. Decompressive surgery was performed through the removal of T7 laminae and the compression materials 6, 9, and 12 weeks after starting compression. Three weeks later, respectively, the neuronal loss in the anterior horn was estimated. RESULTS: The spinal cords were progressively flattened by the expanding of the implanted polymer sheet, and the number of motor neurons in the anterior horn decreased, especially from 6 to 9 weeks after starting compression. Semiquantitative RT-PCR analysis showed that the expression of NGF and BDNF mRNAs was decreased significantly in the spinal cords of 12-week compression group compared with the 6-week compression group and that NGF mRNA expression was up-regulated significantly in the 6-week compression group relative to the 6-week control group. Any changes of expression of other neurotrophic factors were not significant. Since BDNF, not NGF, has been known to be one of the powerful survival factors for spinal motoneurons, we investigated the levelsof BDNF protein in the compressive spinal cords using enzyme immunoassay and immunohistochemistry. We demonstrated the level of BDNF protein in the compressive spinal cords was increased 6 weeks after compression but declined after 12 weeks. The decompressive procedure in the 6 weeks after compression prevented neuronal loss, but the same procedure in the 9 or 12 weeks was ineffective. CONCLUSIONS: From the point of view of neuronal loss, decompressive surgery at an earlier stage, when compensatory mechanisms including the up-regulation of BDNF might be still effective, could provide better therapeutic results against chronic mechanical compressive spinal cord lesions.
机译:研究设计:关于慢性压迫性脊髓中神经元丢失和神经营养因子表达的实验动物研究。目的:研究大鼠慢性压迫性脊髓神经元丢失和神经营养因子的表达,评价减压程序对神经元丢失的影响。背景数据摘要:脊髓的慢性压迫导致前角运动神经元的丢失。但是,这种神经元丢失的确切机制仍不完全了解。此外,尚不确定减压程序是否能阻止这种神经元丢失。方法:在大鼠的T7椎板下显微手术植入一块薄的膨胀聚合物片。 6、9、12和15周后,收集胸脊髓并进行组织病理学检查。使用半定量RT-PCR,酶免疫测定和免疫组化分析神经营养因子的表达,包括NGF,BDNF,NT-3,GDNF,CNTF和VEGF。通过在开始压缩后第6、9和12周去除T7椎板和压缩材料进行减压手术。分别在三周后,估计前角的神经元丢失。结果:植入的聚合物片膨胀使脊髓逐渐变平,前角的运动神经元数量减少,尤其是开始压迫后6至9周。半定量RT-PCR分析显示,与6周压迫组相比,在12周压迫组的脊髓中NGF和BDNF mRNA的表达显着降低,而在6周压迫中NGF mRNA的表达显着上调。压缩组相对于6周对照组。其他神经营养因子的表达没有任何变化。由于已知BDNF(不是NGF)是脊髓运动神经元的强大生存因子之一,因此我们使用酶免疫法和免疫组化方法研究了压迫性脊髓中BDNF蛋白的水平。我们证明了受压脊髓中BDNF蛋白的水平在受压后6周增加,但在12周后下降。压迫后6周的减压程序可防止神经元丢失,但9或12周内的相同程序无效。结论:从神经元损失的角度来看,在早期的减压手术中,包括BDNF上调在内的补偿机制可能仍然有效,可以为慢性机械性压迫性脊髓损伤提供更好的治疗效果。

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