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首页> 外文期刊>Brain research >Noradrenergic lesion of the locus coeruleus increases apomorphine-induced circling behavior and the firing activity of substantia nigra pars reticulata neurons in a rat model of Parkinson's disease.
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Noradrenergic lesion of the locus coeruleus increases apomorphine-induced circling behavior and the firing activity of substantia nigra pars reticulata neurons in a rat model of Parkinson's disease.

机译:在帕金森氏病大鼠模型中,蓝斑能量的去甲肾上腺素损伤增加了阿扑吗啡诱导的盘旋行为和黑质网状神经元的放电活性。

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摘要

The role of noradrenergic depletion of the locus coeruleus (LC) in the pathophysiology of Parkinson's disease (PD) is still unclear. In the present study, apomorphine-induced circling behavior and extracellular firing activity of substantia nigra pars reticulata (SNr) neurons were examined in rats with unilateral 6-hydroxydopamine lesions of the LC, substantia nigra pars compacta (SNc) and with combined SNc and LC lesions. A moderate contralateral circling was observed in rats with LC lesions after apomorphine. Moreover, the circling behavior was obviously increased by further lesions of LC in SNc-lesioned rats. Extracellular recordings indicated that the firing rate of SNr neurons increased significantly and the firing pattern of these neurons also changed towards more irregular and bursty after SNc lesioning as compared to sham-lesioned rats, while the firing rate and pattern were unaffected in rats with simple lesions of the LC. However, the firing rate of SNr neurons in rats with combined LC and SNc lesions increased significantly when compared to that of rats with simple lesions of the SNc, although the firing pattern was not altered. Furthermore, SNc lesions in rats increased the firing rate of SNr neurons with irregular firing pattern, and additional LC lesions in SNc-lesioned rats increased the firing rate of SNr neurons with regular and irregular firing pattern. These results indicate that lesions of the LC intensify apomorphine-induced circling behavior and lead to a further hyperactivity of SNr neurons in a rat model of PD, suggesting that LC-noradrenergic system is involved in the motor dysfunction of PD.
机译:顽固性蓝斑(LC)的去甲肾上腺素耗竭在帕金森氏病(PD)的病理生理学中的作用仍不清楚。在本研究中,在单侧6-羟基多巴胺病变,黑质致密部(SNc)以及SNc和LC合并的大鼠中检查了阿扑吗啡诱导的黑质网状(SNr)神经元的循环行为和细胞外放电活性病变。阿扑吗啡对LC病变大鼠有中等程度的对侧盘旋。此外,SNc损伤的大鼠中LC的进一步损伤明显增强了环行行为。细胞外记录表明,SNc损伤后,SNr神经元的放电速率显着增加,并且这些神经元的放电模式也比假手术损伤的大鼠变得更加不规则和突兀,而简单病变的大鼠的放电速率和模式不受影响。 LC。然而,与LC和SNc合并病变的大鼠相比,SNr神经元的放电速率与单纯SNc病变的大鼠相比明显增加,尽管放电方式没有改变。此外,大鼠的SNc损伤增加了具有不规则放电模式的SNr神经元的放电速率,而SNc损伤的大鼠中的其他LC损伤则增加了具有规则的和不规则放电模式的SNr神经元的放电速率。这些结果表明,LC的损伤加剧了阿朴吗啡诱导的盘旋行为,并导致PD大鼠模型中的SNr神经元进一步活跃,提示LC-去甲肾上腺素系统参与PD的运动功能障碍。

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