首页> 外文期刊>Brain research >Subthalamic nucleus lesions reduce low frequency oscillatory firing of substantia nigra pars reticulata neurons in a rat model of Parkinson's disease.
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Subthalamic nucleus lesions reduce low frequency oscillatory firing 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,丘脑下核损害减少了黑质网状神经元的低频振荡放电。

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Single unit recordings performed in animal models of Parkinson's disease revealed that output nuclei neurons display modifications in firing pattern and firing rate, which are supposed to give rise to the clinical manifestations of the illness. We examined the activity pattern of single units from the substantia nigra pars reticulata, the main output nuclei of the rodent basal ganglia, in urethane-anesthetized control and 6-hydroxydopamine-lesioned rats (a widespread model of Parkinson's disease). We further studied the effect of a subthalamic nucleus lesion in both experimental groups. Subthalamic nucleus lesion produces behavioral improvement in animal models of Parkinson's disease, and was expected to reverse the changes induced by 6-hydroxydopamine lesions. A meticulous statistical investigation, which included a non-biased classification of the recorded units by means of cluster analysis, allowed us to identify a low frequency oscillation of firing rate ( approximately 0.9 Hz) occurring in approximately 35% of the units recorded from 6-hydroxydopamine-lesioned rats, as the main feature differentiating 6-hydroxydopamine-lesioned and control rats. Subthalamic nucleus lesions significantly reduced the proportion of oscillatory units in 6-hydroxydopamine-lesioned rats. However, the population of nigral units recorded from rats bearing both lesions still differed significantly from control units. These results suggest that oscillatory activity in the basal ganglia output nuclei may be related to some clinical features of parkinsonism, and suggest a putative mechanism through which therapeutic interventions aimed at modifying subthalamic nucleus function produce clinical benefit in Parkinson's disease.
机译:在帕金森氏病动物模型中执行的单个单位记录显示,输出核神经元在放电模式和放电率上显示出修饰,这被认为会引起该疾病的临床表现。我们检查了氨基甲酸酯化对照和6-羟基多巴胺损伤大鼠(帕金森氏病的一种普遍模型)中黑质网状结构(啮齿动物基底神经节的主要输出核)的单个单位的活动模式。我们在两个实验组中进一步研究了丘脑下核病变的作用。丘脑下核病变在帕金森氏病动物模型中产生行为改善,并有望逆转6-羟基多巴胺病变引起的变化。细致的统计调查,包括通过聚类分析对记录的单位进行无偏的分类,使我们能够确定在6至3的记录单位中,约有35%发生了发射频率的低频振荡(约0.9 Hz)。羟基多巴胺损伤大鼠是区别6-羟基多巴胺损伤大鼠和对照大鼠的主要特征。丘脑下核损伤显着降低了6-羟基多巴胺损伤大鼠的振荡单位的比例。但是,从同时患有两种病变的大鼠中记录到的黑质单位数量与对照组相比仍存在显着差异。这些结果表明,基底神经节输出核中的振荡活动可能与帕金森氏症的某些临床特征有关,并提出了一种推定的机制,通过该机制,旨在改变丘脑下核功能的治疗干预可在帕金森氏病中产生临床益处。

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