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帕金森病中的尾状核病理学:活检材料的超微结构和生化研究结果

Caudate nucleus pathology in Parkinson's disease: ultrastructural and biochemical findings in biopsy material.

作者信息

Lach B, Grimes D, Benoit B, Minkiewicz-Janda A

机构信息

Department of Laboratory Medicine, Ottawa Civic Hospital, Ontario, Canada.

出版信息

Acta Neuropathol. 1992;83(4):352-60. doi: 10.1007/BF00713525.

Abstract

Ultrastructural and biochemical properties of caudate nucleus (CN) biopsies in two patients with advanced Parkinson's disease (PD) were compared with three CN specimens removed during surgery for intracranial tumors. An additional two specimens from neurologically intact patients (59 and 86 years old) were removed during autopsy (performed 3 and 4 h post mortem, respectively) for electron microscopic studies. Dopamine levels in PD were reduced to less than 15% of control values. Both PD patients showed frequent dystrophic neurites and transsynaptic degeneration of neurons and neuritic processes. These changes were not found in CN from the four control individuals. Only a few dystrophic neurites were noticed in one 67-year-old control patient. The development of neuroaxonal dystrophy in CN is consistent with a dying-back process, probably accompanying abnormalities of axonal transport in PD. Transsynaptic degeneration of neurons in CN very likely represents a morphological marker of disease severity. The occurrence of this change may account for the poor clinical response of patients with advanced PD to intracerebral implantation of dopaminergic tissues.

摘要

将两名晚期帕金森病(PD)患者的尾状核(CN)活检组织的超微结构和生化特性,与三名因颅内肿瘤手术切除的CN标本进行了比较。另外,从两名神经功能正常的患者(分别为59岁和86岁)尸检时(分别在死后3小时和4小时进行)获取了两个标本用于电子显微镜研究。PD患者的多巴胺水平降至对照值的15%以下。两名PD患者均显示出频繁的营养不良性神经突以及神经元和神经突过程的跨突触变性。在四名对照个体的CN中未发现这些变化。仅在一名67岁的对照患者中发现了少数营养不良性神经突。CN中神经轴突营养不良的发展与逆行性变性过程一致,可能伴随着PD中轴突运输异常。CN中神经元的跨突触变性很可能代表疾病严重程度的形态学标志。这种变化的发生可能解释了晚期PD患者对多巴胺能组织脑内植入的临床反应不佳。

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