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首页> 外文期刊>European Spine Journal >Spinal stenosis: assessment of motor function, VEGF expression and angiogenesis in an experimental model in the rat
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Spinal stenosis: assessment of motor function, VEGF expression and angiogenesis in an experimental model in the rat

机译:脊柱狭窄:在大鼠的实验模型中评估运动功能,VEGF表达和血管生成

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摘要

Reduction of blood flow in compressed nerve roots is considered as one important mechanism of induction of neurogenic intermittent claudication in lumbar spinal canal stenosis. Vascular endothelial growth factor (VEGF) is a potent stimulator of angiogenesis, and is increased in expression in hypoxic conditions. The objective of this study was to examine if cauda equina compression affects motor function and induces expression of VEGF and angiogenesis. The cauda equina was compressed by placing a piece of silicone rubber into the L5 epidural space. Walking duration was examined by rota-rod testing. The compressed parts of the cauda equina and L5 dorsal root ganglion (DRG) were removed at 3, 7, 14, or 28 days after surgery, and processed for immunohistochemistry for VEGF and Factor VIII (marker for vascular endothelial cells). Numbers of VEGF-immunoreactive (IR) cells and vascular density were examined. Walking duration was decreased after induction of cauda equina compression. The number of VEGF-IR cells in the cauda equina and DRG was significantly increased at 3, 14, and 28 days after cauda equina compression, compared with sham-operated rats (P < 0.05). Vascular density in the cauda equina was not increased at any of the time points examined. Cauda equina compression decreased walking duration, and induced VEGF expression in nerve roots and DRG.
机译:压缩神经根中血流量的减少被认为是诱导腰椎管狭窄中神经源性间歇性lau行的重要机制之一。血管内皮生长因子(VEGF)是血管生成的有效刺激剂,在缺氧条件下其表达增加。这项研究的目的是检查马尾神经压迫是否影响运动功能并诱导VEGF表达和血管生成。通过将一块硅橡胶放入L5硬膜外腔来压缩马尾神经。通过旋转棒测试检查步行时间。在手术后第3、7、14或28天去除马尾和L5背根神经节(DRG)的压缩部分,并进行VEGF和VIII因子(血管内皮细胞标记)的免疫组织化学处理。检查了VEGF免疫反应(IR)细胞的数量和血管密度。诱导马尾神经受压后步行时间减少。与假手术大鼠相比,马尾压迫后3天,14天和28天,马尾和DRG中的VEGF-IR细胞数量显着增加(P <0.05)。马尾马的血管密度在任何检查的时间点都没有增加。马尾马受压可减少步行时间,并诱导神经根和DRG中的VEGF表达。

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