电刺激加速并增加再生大鼠股运动神经元中BDNF和trkB mRNA的表达。

A. Al-Majed, T. Brushart, T. Gordon
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引用次数: 392

摘要

电刺激促进运动轴突再生的速度和准确性。刺激的积极作用是在细胞体中介导的。在这里,我们描述了电刺激对运动神经元BDNF及其受体trkB表达的影响,这两个基因在运动神经元中的表达水平与再生相关,并受多种神经元的电活动调节。我们采用半定量原位杂交技术,分别在单侧股神经切割、缝合和刺激后8小时、2天和7天,检测编码BDNF和全长trkB受体的mRNA的表达。将再生运动神经元的表达与对侧完整运动神经元的表达进行比较。在股神经缝合和假刺激后8 h和2 d, BDNF和trkB信号没有显著上调。到第7天,BDNF和trkB mRNA的表达增加了2倍。相比之下,仅刺激切割和修复的神经1小时,BDNF和trkB mRNA在前8小时内分别快速上调3倍和2倍。刺激效果在第2天达到峰值,信号分别增加6倍和4倍。此后,BDNF和trkB mRNA的表达水平下降到与神经修复和假刺激后7天的2倍增长相同。我们得出结论,短暂的电刺激可以刺激再生运动神经元中BDNF和trkB的表达。由于已知电刺激可以加速轴突再生,我们认为BDNF和trkB表达的变化与轴突再生的加速有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrical stimulation accelerates and increases expression of BDNF and trkB mRNA in regenerating rat femoral motoneurons.
Electrical stimulation promotes the speed and accuracy of motor axonal regeneration. The positive effects of stimulation are mediated at the cell body. Here we characterize the effect of electrical stimulation on motoneuronal expression of BDNF and its receptor, trkB, two genes whose expression levels in motoneurons correlate with regeneration and are regulated by electrical activity in a variety of neurons. We used semiquantitative in situ hybridization to measure expression of mRNA encoding BDNF and the full-length trkB receptor at intervals of 8 h, 2 days and 7 days after unilateral femoral nerve cut, suture, and stimulation. Expression in regenerating motoneurons was compared to that of contralateral intact motoneurons. BDNF and trkB signals were not significantly upregulated 8 h and 2 days after femoral nerve suture and sham stimulation. By 7 days, there was a 2-fold increase in both BDNF and trkB mRNA expression. In contrast, stimulation of cut and repaired nerves for only 1 h led to rapid upregulation of BDNF and trkB mRNA by 3-fold and 2-fold, respectively, within the first 8 h. The stimulation effect peaked at 2 days with 6-fold and 4-fold increases in the signals, respectively. Thereafter, the levels of BDNF and trkB mRNA expression declined to equal the 2-fold increase seen at 7 days after nerve repair and sham-stimulation. We conclude that brief electrical stimulation stimulates BDNF and trkB expression in regenerating motoneurons. Because electrical stimulation is known to accelerate axonal regeneration, we suggest that changes in the expression of BDNF and trkB correlate with acceleration of axonal regeneration.
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