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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Stimulation of the subthalamic nucleus changes the firing pattern of pallidal neurons.
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Stimulation of the subthalamic nucleus changes the firing pattern of pallidal neurons.

机译:丘脑下核的刺激改变了苍白神经元的放电模式。

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To clarify the mechanism underlying improvement of parkinsonian signs by high-frequency electrical stimulation (HFS) of the subthalamic nucleus (STN), we investigated the effects of STN HFS on neuronal activity of the internal and external segment of the globus pallidus (GPi and GPe, respectively) in two rhesus monkeys rendered parkinsonian by administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. A scaled-down version of the chronic stimulating electrode used in humans, consisting of four metal contacts 0.50 mm in length each separated by 0.50 mm, was implanted through a cephalic chamber targeting the STN. Histological reconstruction revealed that the cathode was located in the STN in both monkeys. Extracellular recordings from a total of 110 pallidal neurons during STN stimulation were performed. Poststimulus time histograms of single neurons triggered by 2 Hz STN stimulation pulses at 2.4-3.0 V revealed short-latency excitations at 2.5-4.5 and 5.5-7.0 msec after stimulation onset and inhibitions at 1.0-2.5, 4.5-5.5, and 7.0-9.0 msec for both GPe and GPi neurons. These short-latency responses were present with 136 Hz stimulation, at voltages effective for alleviation of parkinsonian signs, resulting in a significant increase in mean discharge rate and a stimulus-synchronized regular firing pattern. These results indicate that activation of the STN efferent fibers and resultant changes in the temporal firing pattern of neurons in GPe and GPi underlie the beneficial effect of HFS in the STN in Parkinson's disease and further support the role of temporal firing patterns in the basal ganglia in the development of Parkinson's disease and other movement disorders.
机译:为了阐明丘脑下丘脑核(STN)高频电刺激(HFS)改善帕金森病体征的潜在机制,我们研究了STN HFS对苍白球(GPi和GPe)内部和外部神经元活动的影响分别)在两只恒河猴中通过施用1-甲基-4-苯基-1,2,3,6-四氢吡啶使帕金森病。通过用于STN的头腔植入了按比例缩小版本的人类使用的慢性刺激电极,该电极由四个长度为0.50 mm的金属触点组成,每个触点之间的距离为0.50 mm。组织学重建显示,两只猴子的阴极都位于STN中。在STN刺激过程中,从总共110个苍白神经元进行了细胞外记录。由2 Hz STN刺激脉冲在2.4-3.0 V触发的单个神经元的刺激后时间直方图显示刺激开始后2.5-4.5和5.5-7.0 msec的短时程激发以及1.0-2.5、4.5-5.5和7.0-9.0的抑制GPe和GPi神经元的毫秒数。这些短时延响应在136 Hz刺激下以有效减轻帕金森征兆的电压出现,导致平均放电速率显着提高和刺激同步的常规点火方式。这些结果表明,STN传出纤维的激活以及GPe和GPi中神经元的瞬时放电模式的变化是HFS对STN帕金森病的有益作用,并进一步支持了瞬时放电模式在基底神经节中的作用。帕金森氏病和其他运动障碍的发展。

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