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右侧迷走神经切断术后迷走运动神经元变性的分子分析

Molecular analysis of the vagal motoneuronal degeneration after right vagotomy.

作者信息

Ji Junfeng, Dheen S Thameem, Tay Samuel Sam Wah

机构信息

Department of Anatomy, National University of Singapore, Singapore.

出版信息

J Neurosci Res. 2002 Aug 1;69(3):406-17. doi: 10.1002/jnr.10300.

Abstract

The aim of this study was to investigate the vagal motoneuronal degeneration after right vagotomy using in situ hybridization, RT-PCR, and immunohistochemistry methods. The morphology of the vagal motoneurons in dorsal motor nucleus of the vagus nerve (DMV) and nucleus of ambiguus (NA) after right vagotomy was examined by using Nissl staing and TUNEL. The expression of inducible nitric oxide synthase (iNOS), bcl-2, bax, and caspase-3 in DMV and NA of rats after right vagotomy was studied. Additionally, the involvement of the N-methyl-D-aspartate (NMDA) receptor-calcium-neuronal nitric oxide synthase (nNOS) pathway in the vagal motoneuronal degeneration was addressed by double-immunolabeling analysis of nNOS with NMDAR1 and calbindin D28K in right-vagotomized rats. The neurons in right DMV and NA displayed a darkly stained, shrunken morphology at 1 day and 5 days following right vagotomy as shown by Nissl staining. Quantitative analysis revealed that, at 1 day and 5 days following right vagotomy, the number of neurons in right DMV, but not NA, was significantly reduced in comparison with that of control rats. Occasional TUNEL-positive neurons were detected in right DMV of rat at 1 day after right vagotomy. The expression of iNOS protein and mRNA was absent in DMV and NA of control rats. However, the iNOS mRNA expression was induced bilaterally in DMV and NA at 1 day postoperation and continued to be up-regulated until 5 days after vagotomy as shown by in situ hybridization. Immunohistochemistry analysis also showed the increased expression of iNOS in bilateral DMV and NA of vagotomized rats. RT-PCR analysis revealed the enhanced bcl-2 and reduced bax mRNA levels and subsequent up-regulation of both bcl-2 and bax mRNA in right sides of the vagotomized brainstems at 1 day and 5 days postoperation, respectively. In situ hybridization analysis confirmed the up-regulation of bcl-2 and bax mRNA in right DMV and NA of the rats at 5 days following operation. Immunohistochemistry analysis showed up-regulated Bcl-2 immunoreactivity and undetectable changes in Bax immunoreactivity in DMV and NA of rats at 1 day after vagotomy, whereas enhancement of both Bcl-2 and Bax immunoreactivity was observed at 5 days postoperation. In addition, the caspase-3 mRNA level was elevated ipsilaterally in DMV and NA at 1 day and 5 days following right vagotomy. Double-immunofluorescence analysis showed complete colocalization of nNOS with NMDAR1 and with calbindin in ipsilateral DMV and NA at 10 days following right vagotomy. This study suggests that the signal pathway for NMDAR1-calcium-nNOS and the up-regulation of iNOS in DMV and NA may be involved in the vagal motor neurodgeneration after right vagotomy. Furthermore, our results imply that the apoptosis pathway mediated by Bcl-2, Bax, and caspase-3 may be activated in vagal motoneurons after right vagotomy.

摘要

本研究旨在采用原位杂交、逆转录聚合酶链反应(RT-PCR)和免疫组织化学方法,研究右侧迷走神经切断术后迷走运动神经元的变性情况。采用尼氏染色和末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)检测右侧迷走神经切断术后迷走神经背核(DMV)和疑核(NA)中迷走运动神经元的形态。研究右侧迷走神经切断术后大鼠DMV和NA中诱导型一氧化氮合酶(iNOS)、bcl-2、bax和半胱天冬酶-3的表达。此外,通过对右侧迷走神经切断大鼠的nNOS与NMDAR1和钙结合蛋白D28K进行双重免疫标记分析,探讨N-甲基-D-天冬氨酸(NMDA)受体-钙-神经元型一氧化氮合酶(nNOS)途径在迷走运动神经元变性中的作用。尼氏染色显示,右侧迷走神经切断术后1天和5天,右侧DMV和NA中的神经元呈现深色染色、萎缩的形态。定量分析显示,右侧迷走神经切断术后1天和5天,右侧DMV而非NA中的神经元数量与对照大鼠相比显著减少。右侧迷走神经切断术后1天,在大鼠右侧DMV中偶尔检测到TUNEL阳性神经元。对照大鼠的DMV和NA中未检测到iNOS蛋白和mRNA的表达。然而,原位杂交显示,术后1天DMV和NA双侧均诱导iNOS mRNA表达,并持续上调至迷走神经切断术后5天。免疫组织化学分析也显示,迷走神经切断大鼠双侧DMV和NA中iNOS表达增加。RT-PCR分析显示,术后1天和5天,右侧迷走神经切断脑干中bcl-2 mRNA水平升高,bax mRNA水平降低,随后bcl-2和bax mRNA均上调。原位杂交分析证实,术后5天大鼠右侧DMV和NA中bcl-2和bax mRNA上调。免疫组织化学分析显示,迷走神经切断术后1天,大鼠DMV和NA中Bcl-2免疫反应性上调,Bax免疫反应性无明显变化,而术后5天观察到Bcl-2和Bax免疫反应性均增强。此外,右侧迷走神经切断术后1天和5天,DMV和NA同侧的半胱天冬酶-3 mRNA水平升高。双重免疫荧光分析显示,右侧迷走神经切断术后10天,同侧DMV和NA中nNOS与NMDAR1以及与钙结合蛋白完全共定位。本研究表明,NMDAR1-钙-nNOS信号通路以及DMV和NA中iNOS的上调可能参与右侧迷走神经切断术后的迷走运动神经变性。此外,我们的结果表明,右侧迷走神经切断术后,迷走运动神经元中由Bcl-2、Bax和半胱天冬酶-3介导的凋亡途径可能被激活。

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