首页> 外文期刊>The European Journal of Neuroscience >Unilateral lesion of the nigrostriatal pathway induces an increase of neuronal activity of the pedunculopontine nucleus, which is reversed by the lesion of the subthalamic nucleus in the rat.
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Unilateral lesion of the nigrostriatal pathway induces an increase of neuronal activity of the pedunculopontine nucleus, which is reversed by the lesion of the subthalamic nucleus in the rat.

机译:纹状体纹状体途径的单侧病变诱导了足小神经足核的神经元活性的增加,这被大鼠的丘脑下核的病变所逆转。

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The role of the pedunculopontine nucleus (PPN) in the pathophysiology of Parkinson's disease is still unclear. Using microrecordings, we investigated the changes occurring in PPN neurons after lesions of the substantia nigra compacta (SNc) and the role of the subthalamic nucleus (STN) in these changes. In normal rats the firing rate of PPN neurons was 10.6 +/- 1.4 spikes/s, the majority of neurons (91%) having a regular firing pattern, 6% irregular and 3% in bursts. In rats with 6-hydroxydopamine lesions of the SNc, the firing rate increased significantly to 18.3 +/- 3.0 spikes/s compared with normal rats. In addition, the firing pattern changed significantly: 70% of the neurons discharged regularly, 27% irregularly and 3% in bursts. In rats with ibotenic acid lesions of the STN, the firing rate decreased significantly to 7.2 +/- 0.9 spikes/s and the firing pattern changed significantly: 50% of the neurons discharged regularly, 43% irregularly and 7% in bursts. The rats with combined SNc and STN lesions showed no change in the firing rate (8.5 +/- 1.0 spikes/s) compared to normal rats. The firing pattern changed significantly: 69% of the cells discharged regularly, 26% irregularly and 5% in bursts. These findings demonstrate that PPN neurons are overactive and more irregular in the 6-hydroxydopamine-lesioned rats, suggesting the implication of this nucleus in the pathophysiology of parkinsonism. Moreover, the fact that STN lesions induced a reduction in the firing rate of the PPN in normal rats and a normalization of the firing rate in rats with 6-hydroxydopamine lesions suggests that this nucleus is under major control of the STN.
机译:pedunculopontine核(PPN)在帕金森氏病病理生理中的作用仍不清楚。使用微记录,我们调查了黑质致密部(SNc)病变后PPN神经元中发生的变化以及丘脑底核(STN)在这些变化中的作用。在正常大鼠中,PPN神经元的放电速率为10.6 +/- 1.4峰值/秒,大多数神经元(91%)具有规则的放电模式,有6%的不规则放电和3%的突发放电。与正常大鼠相比,在具有SNc 6-羟基多巴胺损伤的大鼠中,放电频率显着提高至18.3 +/- 3.0峰值/秒。此外,放电模式也发生了显着变化:70%的神经元规则放电,27%不规则放电和3%突然放电。在患有STN的卵磷脂酸损伤的大鼠中,放电速率显着降低至7.2 +/- 0.9峰值/秒,放电模式也发生了显着变化:50%的神经元规则放电,43%的不规则放电和7%的爆发。与正常大鼠相比,合并有SNc和STN病变的大鼠的放电频率没有变化(8.5 +/- 1.0峰值/秒)。发射模式发生了显着变化:69%的细胞规则放电,26%的规则放电和5%的爆发。这些发现表明,在6-羟基多巴胺损伤的大鼠中,PPN神经元过度活跃,并且更加不规则,提示该核在帕金森氏症的病理生理中具有重要意义。此外,STN损伤会导致正常大鼠PPN放电速率降低,而6-羟基多巴胺损伤的大鼠的放电速率正常化这一事实表明,该核受STN的主要控制。

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