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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Pallidal origin of GABA release within the substantia nigra pars reticulata during high-frequency stimulation of the subthalamic nucleus.
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Pallidal origin of GABA release within the substantia nigra pars reticulata during high-frequency stimulation of the subthalamic nucleus.

机译:在高频刺激丘脑下核的过程中,黑质内网状组织释放的GABA的苍白起源。

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High-frequency stimulation of the subthalamic nucleus (HFS-STN) is an effective treatment for alleviating the motor symptoms of parkinsonian patients. However, the neurochemical basis of its effects remains unknown. We showed previously that 1 h of HFS-STN in normal rats increases extracellular glutamate (Glu) level in the output nuclei of the STN, the globus pallidus (GP), and the substantia nigra pars reticulata (SNr), consistent with an increase in the activity of STN neurons. HFS-STN also increases GABA levels in the SNr, but the origin of this increase is unclear. We investigated the effectiveness of HFS-STN for improving Parkinson's disease symptoms, using intracerebral microdialysis to determine the extracellular Glu and GABA levels of the GP and SNr in response to HFS-STN in anesthetized hemiparkinsonian rats [6-hydroxydopamine lesion of the substantia nigra pars compacta (SNc)]. Basal levels of Glu and GABA in the GP and SNr were significantly higher in hemiparkinsonian than in intact rats. HFS-STN did not affect extracellular Glu level in the SNr of hemiparkinsonian rats but doubled the level of GABA. Ibotenic acid lesion of the GP abolished the increase in GABA levels in the SNr induced by HFS-STN in SNc-lesioned rats. These results provide neurochemical confirmation of the hyperactivity of the STN after dopaminergic denervation and suggest that the therapeutic effects of HFS-STN may result partly from the stimulation of pallidonigral fibers, thereby revealing a potential role for pallidal GABA in the inhibition of basal ganglial output structures during HFS-STN.
机译:高频刺激丘脑底核(HFS-STN)是缓解帕金森氏病患者运动症状的有效方法。但是,其作用的神经化学基础仍然未知。我们先前显示正常大鼠中的HFS-STN 1小时会增加STN,苍白球(GP)和黑质网状组织(SNr)的输出核中的细胞外谷氨酸(Glu)水平,与STN神经元的活动。 HFS-STN也会增加SNr中的GABA水平,但这种增加的原因尚不清楚。我们研究了HFS-STN改善帕金森氏病症状的有效性,使用脑内微透析测定麻醉的半帕金森病大鼠[黑质6-羟基多巴胺病变,对HFS-STN的反应] GP和SNr的细胞外Glu和GABA水平Compacta(SNc)]。半帕金森病患者的GP和SNr中Glu和GABA的基础水平显着高于完整大鼠。 HFS-STN不会影响偏帕金森氏病大鼠SNr中的细胞外Glu水平,但会使GABA水平增加一倍。 GP的伊波烯酸损害消除了SNc损害的大鼠中HFS-STN诱导的SNr中GABA水平的升高。这些结果提供了神经化学证实多巴胺能去神经后STN的过度活跃,并提示HFS-STN的治疗作用可能部分源于刺激苍白顶神经纤维,从而揭示了苍白GABA在抑制基底神经节输出结构中的潜在作用。在HFS-STN期间。

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