Dopaminergic innervation of the human subventricular zone: a comparison between Huntington's chorea and Parkinson's disease.

American journal of neurodegenerative disease Pub Date : 2013-09-18 eCollection Date: 2013-01-01
Martin Parent, C Bédard, E Pourcher
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Abstract

The subventricular zone retains its neurogenic capacity throughout life and, as such, is often considered a potential source for endogenous repair in neurodegenerative disorders. Because dopamine is believed to stimulate adult neurogenesis, we looked for possible variations in the dopaminergic innervation of the subventricular zone between cases of Huntington's chorea and Parkinson's diseases. Antibodies against tyrosine hydroxylase (TH) and proliferating cell nuclear antigen (PCNA) were used as specific markers of dopaminergic axons and cell proliferating activity, respectively. The immunohistochemical approach was applied to postmortem tissue from 2 Parkinson's disease cases, 4 Huntington's disease cases, along with age-matched controls. The immunostaining was revealed with either diaminobenzidine or fluorescent-conjugated secondary antibodies. Optical density measurements were made along the entire dorso-ventral extent of the caudate nucleus. An intense TH+ zone was detected along the ventricular border of the caudate nucleus in Huntington's disease cases, but not in patients with Parkinson's disease or age-matched controls. This thin (287±38 μm) paraventricular zone was composed of numerous small and densely packed dopamine axon varicosities and overlapped the deep layers of the subventricular zone. Its immunoreactivity was 47±8% more intense than that of adjacent striatal areas. The dopamine innervation of the subventricular zone is strikingly massive in Huntington's chorea compared to Parkinson's disease, a finding that concurs with the marked increase in neurogenesis noted in the subventricular zone of Huntington's disease patients. This finding suggests that dopamine plays a crucial role in mechanisms designed to compensate for the massive striatal neuronal losses that occur in Huntington's disease.

人类脑室下区的多巴胺能神经支配:亨廷顿舞蹈症与帕金森病的比较。
室管膜下区终生保持其神经源能力,因此通常被认为是神经退行性疾病内源性修复的潜在来源。由于多巴胺被认为能刺激成人神经发生,因此我们研究了亨廷顿舞蹈症和帕金森病患者室管膜下区多巴胺能神经支配的可能变化。酪氨酸羟化酶(TH)和增殖细胞核抗原(PCNA)抗体分别被用作多巴胺能轴突和细胞增殖活性的特异性标记物。免疫组化方法适用于 2 例帕金森病病例、4 例亨廷顿病病例以及年龄匹配的对照组的死后组织。使用二氨基联苯胺或荧光结合的二抗进行免疫染色。光密度测量沿着尾状核的整个背腹进行。在亨廷顿氏病患者中,沿着尾状核的脑室边界检测到了一个强烈的TH+区,但在帕金森氏病患者或年龄匹配的对照组中却没有发现。这个薄薄的(287±38 μm)室旁区由许多小而密集的多巴胺轴突变节组成,并与室下区的深层重叠。其免疫反应强度比邻近纹状体区域高47±8%。与帕金森病相比,亨廷顿舞蹈症患者室下区的多巴胺神经支配明显增加,这一发现与亨廷顿舞蹈症患者室下区神经发生的明显增加相吻合。这一发现表明,多巴胺在亨廷顿舞蹈症患者纹状体神经元大量缺失的补偿机制中起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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