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帕金森病中延髓内C1和C3肾上腺素能合成神经元的缺失。

Loss of C1 and C3 epinephrine-synthesizing neurons in the medulla oblongata in Parkinson's disease.

作者信息

Gai W P, Geffen L B, Denoroy L, Blessing W W

机构信息

Department of Physiology, Flinders Medical Centre, Bedford Park, SA.

出版信息

Ann Neurol. 1993 Apr;33(4):357-67. doi: 10.1002/ana.410330405.

Abstract

We used immunohistochemical analysis to determine whether medulla oblongata neurons containing phenylethanolamine N-methyltransferase (PNMT) are affected in patients who died with idiopathic Parkinson's disease (n = 7) compared with age-matched control subjects who died with nonneurological diseases (n = 8). Transverse sections (50 microns) of medulla were prepared either for conventional neuropathological examination or for the immunohistochemical demonstration of PNMT. Immunopositive neurons at approximately 30 rostrocaudal levels, evenly spaced throughout the whole medulla, were mapped and cells in each section were counted with a camera lucida system linked to a computer. In the ventrolateral medulla, from the level of the obex to 11 mm rostral to the obex where the C1 group of neurons is located, there were 7,631 +/- 844 PNMT-positive neurons in control brains and 3,604 +/- 1,051 in brains affected by Parkinson's disease (47% of control). Many PNMT-positive neurons contained Lewy bodies. We observed a previously undescribed midline (C3) group of PNMT-positive neurons in normal brains, and this group was also severely affected (12% of control) in parkinsonian brains. Neither the C2 group nor the small PNMT-positive neurons in the nucleus tractus solitarii were significantly reduced in numbers but there was a reduction in the numbers of melanin-pigmented cells in both the ventrolateral (50% of control) and the dorsomedial (79% of control) region. Our results demonstrate a selective loss of C1 and C3 PNMT-positive neurons, providing the first quantitative evidence for damage to these presumed brainstem sympathetic premotor neurons in Parkinson's disease. These changes may underlie some of the autonomic symptoms occurring in this condition.

摘要

我们采用免疫组化分析,以确定与死于非神经疾病的年龄匹配对照受试者(n = 8)相比,死于特发性帕金森病的患者(n = 7)中含苯乙醇胺N-甲基转移酶(PNMT)的延髓神经元是否受到影响。制备延髓的横切片(50微米)用于常规神经病理学检查或PNMT的免疫组化显示。在整个延髓均匀分布的大约30个前后水平的免疫阳性神经元被定位,并且每个切片中的细胞通过连接到计算机的明视野系统进行计数。在延髓腹外侧,从闩部水平到闩部头侧11毫米处(C1组神经元所在位置),对照脑中存在7631±844个PNMT阳性神经元,而帕金森病患者脑中为3604±1051个(为对照的47%)。许多PNMT阳性神经元含有路易小体。我们在正常脑中观察到一个先前未描述的中线(C3)组PNMT阳性神经元,并且该组在帕金森病脑中也受到严重影响(为对照的12%)。孤束核中的C2组神经元和小PNMT阳性神经元数量均未显著减少,但腹外侧(为对照的50%)和背内侧(为对照的79%)区域的黑色素细胞数量减少。我们的结果表明C1和C3 PNMT阳性神经元选择性丢失,为帕金森病中这些推测的脑干交感神经运动前神经元受损提供了首个定量证据。这些变化可能是该疾病中出现的一些自主神经症状的基础。

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