首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Subthalamic nucleus and globus pallidus interna influence firing of tonically active neurons in the primate striatum through different mechanisms
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Subthalamic nucleus and globus pallidus interna influence firing of tonically active neurons in the primate striatum through different mechanisms

机译:丘脑下核和苍白球间核通过不同机制影响灵长类纹状体中调性活动神经元的放电

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摘要

Both the subthalamic nucleus (STN) and the globus pallidus pars interna (GPi) are major targets for neuromodulation therapy for movement disorders. An example of such a therapy is deep brain stimulation (DBS). The striatum is the primary target for pharmacological treatment of these disorders. To further our understanding of both the functional relationships among motor nuclei and the mechanisms of therapies for movement disorders, it is important to clarify how changing the neuronal activity of one target, either by medication or by artificial electrical stimulation, affects the other connected nuclei. To investigate this point, we recorded single‐unit activity from tonically active neurons (TANs), which are putative cholinergic interneurons in the striatum, of healthy monkeys (Macaca fuscata) during electrical stimulation of the STN or GPi. Both STN stimulation and GPi stimulation reduced the TAN spike rate. Local infusion of a D2 receptor antagonist in the striatum blocked the reduction in spike rate induced by STN stimulation but not that induced by GPi stimulation. Further, STN stimulation induced phasic dopamine release in the striatum as revealed by in vivo fast‐scan cyclic voltammetry. These results suggest the presence of multiple, strong functional relationships among the STN, GPi, and striatum that have different pathways and imply distinct therapeutic mechanisms for STN‐ and GPi‐ style="fixed-case">DBS.
机译:丘脑底核(STN)和苍白球间(GPi)都是运动障碍神经调节治疗的主要靶标。这种疗法的一个例子是脑深部刺激(DBS)。纹状体是这些疾病的药物治疗的主要目标。为了进一步了解运动核之间的功能关系和运动障碍的治疗机制,重要的是阐明通过药物或人工电刺激改变一个靶标的神经元活动如何影响另一个相连的核。为了研究这一点,我们记录了STN或GPi电刺激过程中健康猴子(猕猴)纹状体中假定的胆碱能中间神经元-调性神经元(TANs)的单单位活性。 STN刺激和GPi刺激均可降低TAN尖峰率。在纹状体中局部输注D2受体拮抗剂可阻止STN刺激引起的刺突率降低,而GPi刺激则不会。此外,如体内快速扫描循环伏安法所示,STN刺激诱导纹状体中的多巴胺释放。这些结果表明,STN,GPi和纹状体之间存在多种牢固的功能关系,它们具有不同的途径,暗示着STN-和GPi- style =“ fixed-case”> DBS 的独特治疗机制。

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