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部分损伤大鼠黑质多巴胺能神经元的电生理特性:丘脑底核切开术和左旋多巴治疗的影响

Electrophysiological characterization of substantia nigra dopaminergic neurons in partially lesioned rats: effects of subthalamotomy and levodopa treatment.

作者信息

Bilbao Gaizka, Ruiz-Ortega Jose Angel, Miguens Natalia, Ulibarri Isabel, Linazasoro Gurutz, Gómez-Urquijo Sonia, Garibi Jesús, Ugedo Luisa

机构信息

Department of Neurosurgery, Cruces Hospital E-48903, Bizkaia, Spain.

出版信息

Brain Res. 2006 Apr 21;1084(1):175-84. doi: 10.1016/j.brainres.2006.02.052. Epub 2006 Mar 30.

Abstract

Progressive degeneration of dopaminergic neurons in the substantia nigra pars compacta is the main histopathological characteristic of Parkinson's disease. We studied the electrophysiological characteristics of the spontaneous activity of substantia nigra pars compacta dopaminergic neurons in rats with a partial, unilateral, 6-hydroxydopamine lesion of the nigrostriatal pathway. In addition, the effects of subthalamotomy and prolonged levodopa treatment on the activity of dopaminergic neurons were investigated. As a result of the lesion ( approximately 50% neuronal loss), the number of spontaneously active neurons was significantly reduced. Basal firing rate, burst firing and responsiveness to intravenously administered apomorphine remained unchanged. In contrast, the variation coefficient, a measure of interspike interval regularity, was significantly increased. Ibotenic acid (10 microg) lesion of the ipsilateral subthalamic nucleus in lesioned rats did not modify the electrophysiological parameters. However, prolonged levodopa treatment (100 mg/kg/day + benserazide 25 mg/kg/day, 14 days) reversed the irregularity observed in cells from lesioned rats, while it induced an irregular firing pattern in cells from intact rats. Our results using an experimental model of moderate Parkinson's disease indicate that surviving substantia nigra pars compacta dopaminergic neurons fire irregularly. In this model, subthalamotomy does not modify the firing pattern while levodopa treatment efficiently restores normal firing of SNpc neurons and does not appear to be toxic to them.

摘要

黑质致密部多巴胺能神经元的进行性退变是帕金森病的主要组织病理学特征。我们研究了单侧6-羟基多巴胺部分损毁黑质纹状体通路大鼠黑质致密部多巴胺能神经元自发放电活动的电生理特性。此外,还研究了丘脑底核切开术和长期左旋多巴治疗对多巴胺能神经元活动的影响。由于损伤(约50%的神经元丢失),自发放电神经元的数量显著减少。基础放电频率、爆发式放电以及对静脉注射阿扑吗啡的反应性均保持不变。相比之下,衡量峰电位间隔规律性的变异系数显著增加。对损伤大鼠同侧丘脑底核进行异搏亭酸(10微克)损毁并未改变电生理参数。然而,长期左旋多巴治疗(100毫克/千克/天+苄丝肼25毫克/千克/天,14天)可逆转损伤大鼠细胞中观察到的不规则放电,同时却在正常大鼠细胞中诱导出不规则放电模式。我们使用中度帕金森病实验模型的研究结果表明,存活的黑质致密部多巴胺能神经元放电不规则。在该模型中,丘脑底核切开术不会改变放电模式,而左旋多巴治疗可有效恢复黑质致密部神经元的正常放电,且似乎对其无毒害作用。

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