帕金森病患者尾状核的突触可塑性

Philippe Anglade, Annick Mouatt-Prigent, Yves Agid, Etienne C. Hirsch
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引用次数: 117

摘要

帕金森病(PD)中黑质多巴胺能神经元的缺失可能会引起黑质纹状体通路中细胞相互作用的重组。事实上,在6-羟多巴胺引起黑质损伤的大鼠纹状体中,皮质纹状体突触的可塑性已经得到证实。然而,据我们所知,纹状体的突触可塑性尚未在人类PD中进行过研究。在本研究中,我们在电子显微镜水平上分析了3例PD患者和3例匹配对照的尾状核神经元树突棘与传入神经不对称接触形成的突触的形态特征。PD患者突触后密度长度和穿孔突触数量均显著增加(分别为24%和88%);这些传入神经的大小和线粒体占据的表面积也显示出增加(分别为24%和50%),尽管没有统计学意义。树突棘的大小和密度以及突触后密度穿孔的大小没有变化。这些数据表明PD中假定的皮质纹状体突触存在可塑性,并提示皮质传入神经对gaba能神经元的过度活跃。
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Synaptic Plasticity in the Caudate Nucleus of Patients with Parkinson's Disease

The loss of dopaminergic neurons from the substantia nigra in Parkinson's disease (PD) may provoke a reorganization of cellular interactions in the nigrostriatal pathway. Indeed, a plasticity of putative corticostriatal synapses has been evidenced in the striatum of rats with a 6-hydroxydopamine-induced lesion of the substantia nigra. However, to our knowledge, synaptic plasticity in the striatum has not previously been investigated in human PD. In this study, we have analysed, at electron microscope level, the morphological characteristics of the synapses formed by afferents in asymmetric contact with dendritic spines of neurons in the caudate nucleus of three patients with PD and three matched controls. The length of the postsynaptic densities and the number of perforated synapses were both significantly increased (24 and 88%, respectively) in the PD patients; the size of these afferents and the surface area occupied by their mitochondria also showed an increase (24 and 50%, respectively), although not statistically significant. The size and density of dendritic spines and the size of postsynaptic density perforations were unchanged. These data indicate the presence of plasticity of the putative corticostriatal synapses in PD and suggest a hyperactivity of cortical afferents to GABAergic neurons.

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