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首页> 外文期刊>Revista Brasileira de Ortopedia >Express?o de neurotrofinas e avalia??o histomorfométrica em ratos Wistar submetidos à mobiliza??o neural após compress?o do nervo mediano
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Express?o de neurotrofinas e avalia??o histomorfométrica em ratos Wistar submetidos à mobiliza??o neural após compress?o do nervo mediano

机译:Wistar大鼠正中神经压迫后神经动员后神经营养蛋白的表达和组织形态计量学评估

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Objective To evaluate the neurotrophin mRNA expression and axon count in the median nerve of Wistar rats submitted to neural mobilization (NM) after nerve compression. Methods Eighteen animals were randomly divided into G1 (nerve compression only), G2 (NM for 1 ? minute), and G3 (NM for 3 ? minutes). For NM, the animals were anesthetized and the right scapula received the mobilization, adapted as indicated for humans, on alternate days, from the third to the 13th postoperative (PO) day, totaling six days of therapy. On the 14th PO day, animals were anesthetized and euthanized. Fragments of the median nerve, distal to the compression procedure, were removed for histomorphometric analysis and expression of neurotrophins, nerve growth factor (NGF), and brain‐derived neurotrophic factor (BDNF) by RT‐PCR. Results Histomorphometric analysis revealed differences in the number of axons in the injured side, which was significantly lower in the injured limb nerve compared to the control limb, whereas the RT‐PCR analysis showed no significant differences in the expression of NGF or BDNF. Conclusion NM treatment did not affect median nerve regeneration, which maintained normal recovery rates.
机译:目的评估Wistar大鼠神经压迫后神经动员(NM)神经中枢神经营养因子mRNA的表达和轴突计数。方法将18只动物随机分为G1(仅神经压迫),G2(NM为1分钟)和G3(NM为3分钟)。对于NM,将动物麻醉,并在术后第3天至第13天(隔天)隔天,按人的指示对动骨进行动员,并按照人类指示进行适应。在采购订单的第14天,将动物麻醉并安乐死。通过RT-PCR去除压缩过程远端的正中神经碎片,以进行组织形态分析,并表达神经营养蛋白,神经生长因子(NGF)和脑源性神经营养因子(BDNF)。结果组织形态计量学分析显示,受伤侧的轴突数量存在差异,与对照肢体相比,受伤肢体神经中轴突的数量明显减少,而RT-PCR分析显示NGF或BDNF的表达没有显着差异。结论NM治疗不影响正中神经再生,恢复正常。

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