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Spontaneous and Evoked Activity of Substantia Nigra Pars Reticulata Neurons during High-Frequency Stimulation of the Subthalamic Nucleus

机译:丘脑下核的高频刺激过程中黑质黑质网状神经元的自发和诱发活动

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摘要

The subthalamic nucleus (STN), a major component of the basal ganglia, exerts an excitatory influence on the output structures of this system i.e., the substantia nigra pars reticulata (SNR) and the internal segment of the globus pallidus. High-frequency stimulation of the STN is a method currently used to treat parkinsonian symptoms. The aim of the present study was to analyze the effects of STN high-frequency stimulation on the activity of SNR neurons and to investigate its impact on the transfer of information between the cerebral cortex and the SNR. During STN high-frequency stimulation, the activity of SNR cells was decreased at low-intensity stimulation, whereas it was increased at a higher intensity. The decrease in the discharge of SNR cells likely results from the activation of a GABAergic transmission in the SNR because this effect was blocked by local application of bicuculline. The increased activity likely results from the activation of the glutamatergic subthalamonigral projection because the latency of the evoked excitations was consistent with the conduction time of the subthalamonigral neurons. Finally, during STN high-frequency stimulation, the transmission of cortical information along the direct trans-striatal pathway was preserved, whereas the functionality of the trans-subthalamic pathways was partly preserved or completely blocked depending on the stimulation intensity. The present data indicate that STN high-frequency stimulation influences the activity of SNR cells through activation of their excitatory and inhibitory synaptic afferent pathways as well as antidromic activation of the projection neurons.
机译:丘脑底核(STN)是基底神经节的主要组成部分,对该系统的输出结构即黑质网状黑质(SNR)和苍白球的内部部分产生兴奋性影响。 STN的高频刺激是目前用于治疗帕金森氏症状的方法。本研究的目的是分析STN高频刺激对SNR神经元活动的影响,并研究其对大脑皮层与SNR之间信息传递的影响。在STN高频刺激过程中,低强度刺激会降低SNR细胞的活性,而强度较高时会增加。 SNR细胞放电的减少可能是由于SNR中GABA能传递的激活所致,因为这种作用被双小分子的局部应用所阻断。活性的增加可能是由于谷氨酸能的丘脑下神经突投射的激活所致,因为诱发的兴奋的潜伏期与丘脑下神经元的传导时间一致。最终,在STN高频刺激过程中,沿直接跨纹状体途径的皮质信息传递得以保留,而根据刺激强度,跨丘脑底途径的功能被部分保留或完全阻断。目前的数据表明,STN高频刺激通过激活它们的兴奋性和抑制性突触传入通路以及投射神经元的抗皮肤激活来影响SNR细胞的活性。

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