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正中神经受压后接受神经松动术的Wistar大鼠神经营养因子表达及组织形态计量学评估

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

作者信息

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

机构信息

Universidade Estadual do Oeste do Paraná (Unioeste), Cascavel, PR, Brazil.

Programa de Ciências Farmacêuticas, Universidade Estadual do Oeste do Paraná (Unioeste), Cascavel, PR, Brazil.

出版信息

Rev Bras Ortop. 2018 Apr 4;53(3):276-280. doi: 10.1016/j.rboe.2018.03.006. eCollection 2018 May-Jun.

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.

摘要

目的

评估神经受压后接受神经松动术(NM)的Wistar大鼠正中神经中神经营养因子mRNA表达及轴突数量。

方法

18只动物随机分为G1组(仅神经受压)、G2组(NM 1分钟)和G3组(NM 3分钟)。对于NM,动物麻醉后,右侧肩胛骨接受松动术,按照人类适用的方法进行调整,术后第3天至第13天隔天进行,共治疗6天。术后第14天,动物麻醉并处死。切除压迫操作远端的正中神经片段,进行组织形态计量分析,并通过逆转录聚合酶链反应(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

组织形态计量分析显示,损伤侧轴突数量存在差异,与对照肢体相比,损伤肢体神经中的轴突数量显著减少,而RT-PCR分析显示NGF或BDNF的表达无显著差异。

结论

NM治疗不影响正中神经再生,正中神经再生维持正常恢复率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/5993878/88fc5af26d7f/gr1.jpg

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