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丘脑底核高频刺激期间黑质网状部内GABA释放的苍白球起源

Pallidal origin of GABA release within the substantia nigra pars reticulata during high-frequency stimulation of the subthalamic nucleus.

作者信息

Windels François, Carcenac Carole, Poupard Annie, Savasta Marc

机构信息

Dynamique des Réseaux Neuronaux, Unité Mixte de Recherche, Institut National de la Santé et de la Recherche Médicale, Université Joseph Fourier, 38041 Grenoble Cedex 09, France.

出版信息

J Neurosci. 2005 May 18;25(20):5079-86. doi: 10.1523/JNEUROSCI.0360-05.2005.

Abstract

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.

摘要

高频刺激丘脑底核(HFS - STN)是缓解帕金森病患者运动症状的一种有效治疗方法。然而,其作用的神经化学基础仍不清楚。我们先前表明,正常大鼠中1小时的HFS - STN会增加丘脑底核输出核团、苍白球(GP)和黑质网状部(SNr)的细胞外谷氨酸(Glu)水平,这与丘脑底核神经元活动增加一致。HFS - STN还会增加SNr中的GABA水平,但这种增加的来源尚不清楚。我们使用脑内微透析来测定麻醉的偏侧帕金森病大鼠[黑质致密部(SNc)6 - 羟基多巴胺损伤]中GP和SNr对HFS - STN反应时的细胞外Glu和GABA水平,研究了HFS - STN改善帕金森病症状的有效性。偏侧帕金森病大鼠中GP和SNr的Glu和GABA基础水平显著高于正常大鼠。HFS - STN不影响偏侧帕金森病大鼠SNr中的细胞外Glu水平,但使GABA水平增加了一倍。GP的鹅膏蕈氨酸损伤消除了SNc损伤大鼠中HFS - STN诱导的SNr中GABA水平的增加。这些结果为多巴胺能去神经支配后丘脑底核的活动亢进提供了神经化学证据,并表明HFS - STN的治疗效果可能部分源于对苍白球 - 黑质纤维的刺激,从而揭示了苍白球GABA在HFS - STN期间对基底神经节输出结构抑制中的潜在作用。

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