Rats with Partial Unilateral Nigrostriatal Lesions as a Model for Studying CNS Plasticity

F. Junn, T. Collier, S. Felten, D. Gash
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引用次数: 1

Abstract

We describe the methods and rationale for using rats with a partial unilateral lesion of the nigrostriatal system as an animal model for studying neural plasticity in both young and aged brains. The rats are lesioned with 6-hydroxydopamine injected into the substantia nigra or the medial forebrain bundle. Amphetamine- and apomorphine-induced rotational behaviors are tested 3 and 4 weeks following the lesion. Based on the rotational responses to amphetamine and apomorphine administration, animals can be classified into one of three groups: unaffected, partially lesioned, or severely lesioned. Animals classified as displaying unaffected rotational behavior are those that do not respond to either amphetamine or apomorphine stimulation. Partially lesioned animals rotate ipsilateral to the lesioned side upon amphetamine injection, but do not display a significant number of rotations in response to apomorphine administration. In contrast, severely lesioned rats rotate after both amphetamine and apomorphine injections. Cell counts reveal that the mean number of dopamine neurons in the ventral mesencephalon of partially lesioned animals is reduced to 40% of that of the intact side. Also in partially lesioned animals, dopamine concentrations on the lesion side are even more severely depleted, averaging about 20% of levels in the contralateral intact striatum. Striatal dopamine concentrations correlate well with the number of surviving dopamine neurons in the ventral mesencephalon (r2 = 0.66, P < 0.05). Amphetamine-induced rotation rates also show a moderate correlation with both striatal dopamine concentrations and mesencephalic dopamine neuron cell counts. Therefore, rotational behavior induced by amphetamine and apomorphine stimulation can be used to identify partially lesioned rats following unilateral 6-hydroxydopamine lesions. It is also possible to estimate the extent of nigrostriatal system damage from the rate of amphetamine-induced rotation.
单侧黑质纹状体部分损伤大鼠作为研究中枢神经系统可塑性的模型
我们描述了使用单侧黑质纹状体部分损伤的大鼠作为研究年轻和老年大脑神经可塑性的动物模型的方法和原理。将6-羟多巴胺注入黑质或内侧前脑束损伤大鼠。在病变后3周和4周检测安非他明和阿帕吗啡诱导的旋转行为。根据对安非他明和阿波啡的轮流反应,动物可分为三组:未受影响、部分受损或严重受损。被归类为显示未受影响的旋转行为的动物是那些对安非他明或阿波啡刺激没有反应的动物。部分损伤的动物在注射安非他明后向损伤侧旋转,但在阿波啡给药后没有明显的旋转。相比之下,严重损伤的大鼠在注射安非他明和阿波啡后都旋转。细胞计数显示,部分损伤动物腹侧中脑多巴胺神经元的平均数量减少到完好侧的40%。同样,在部分受损的动物中,受损侧的多巴胺浓度甚至更为严重,平均约为对侧完整纹状体水平的20%。纹状体多巴胺浓度与中脑腹侧多巴胺神经元存活数呈正相关(r2 = 0.66, P < 0.05)。安非他明诱导的旋转速率也显示出纹状体多巴胺浓度和中脑多巴胺神经元细胞计数的适度相关性。因此,安非他明和阿波啡刺激诱导的旋转行为可用于识别单侧6-羟多巴胺损伤后部分损伤的大鼠。也可以从安非他明引起的旋转速率来估计黑质纹状体系统损伤的程度。
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