Neurotrophin expression and histomorphometric evaluation in Wistar rats subjected to neural mobilization after compression of the median nerve

Marieli Araujo Rossoni Marcioli , José Luis da Conceição Silva , Lucinéia de Fátima Chasko Ribeiro , Rose Meire Costa Brancalhão , Gladson Ricardo Flor Bertolini
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引用次数: 3

Abstract

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 min), and G3 (NM for 3 min). 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.

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正中神经受压后神经活动Wistar大鼠神经营养因子表达及组织形态计量学评价
目的观察Wistar大鼠神经压迫后神经动员(NM)正中神经中神经营养因子mRNA表达及轴突计数的变化。方法18只动物随机分为G1(仅压迫神经)、G2(麻醉1 min)和G3(麻醉3 min)。对于NM,从术后第3天到第13天,隔天麻醉动物,并按照人类的指示活动右肩胛骨,共治疗6天。在第14 PO天,对动物进行麻醉和安乐死。取离压迫手术远端的正中神经碎片,进行组织形态学分析,并通过RT-PCR检测神经营养因子、神经生长因子(NGF)和脑源性神经营养因子(BDNF)的表达。结果形态学分析显示,损伤侧神经轴突数量明显低于正常肢体,而RT-PCR分析显示NGF和BDNF的表达差异无统计学意义。结论纳米治疗不影响正中神经再生,保持了正常的恢复速度。
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