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一例成人起病的单纯苍白球变性。II. 神经递质标志物分析,特别提及苍白球丘脑束在人脑的终末情况。

A case of adult onset pure pallidal degeneration. II. Analysis of neurotransmitter markers, with special reference to the termination of pallidothalamic tract in human brain.

作者信息

Aizawa H, Kwak S, Shimizu T, Mannen T, Shibasaki H

机构信息

National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.

出版信息

J Neurol Sci. 1991 Mar;102(1):83-91. doi: 10.1016/0022-510x(91)90097-q.

Abstract

We analyzed neurotransmitter markers in a brain of a very rare case of pathologically confirmed adult-onset pure pallidal degeneration (PPD) as compared with 16 controls. Neurotransmitter concentrations are significantly altered in the globus pallidus (GP), subthalamic nucleus (ST) and the thalamic nuclei. Concentrations of gamma-aminobutyric acid (GABA) in the external segment (GPe) and internal segment (GPi) of GP and ST are decreased to 62, 45 and 55% of the control mean, respectively. Concentrations of glutamic acid are increased in GPi (144%) and ST (134%). Choline acetyltransferase (ChAT) activities are increased in GPe (232%), GPi (218%), ST (161%), and ventroanterior (VA, 210%) and ventrolateral nucleus (VL, 193%) of the thalamus. Noradrenaline (NA) concentrations in GPe and GPi are 56 and 43% of the control mean, respectively. Dopaminergic and serotonergic systems show no remarkable change. The grid microdissection analysis demonstrates a patchy GABA distribution in the thalamus of 3 controls, whereas a small GABA-rich area in the ventro-oral nucleus (VO) according to the atlas of Hopf disappears in adult onset PPD. These results strongly suggest that (1) GP GABAergic neurons are selectively degenerated and striatopallidal GABAergic nerve terminals are hypoactive; (2) ChAT activities in GP, ST, VA and VL are increased; (3) the subthalamopallidal glutamatergic system is not hypoactive; (4) activity of the noradrenergic system in GP is decreased; and that (5) VO in the thalamus specifically receives GABAergic nerve terminals from GP in human brain.

摘要

我们分析了一例经病理证实的成人起病的纯苍白球变性(PPD)极为罕见病例的大脑中的神经递质标志物,并与16名对照者进行了比较。苍白球(GP)、丘脑底核(ST)和丘脑核团中的神经递质浓度发生了显著变化。GP外侧段(GPe)和内侧段(GPi)以及ST中的γ-氨基丁酸(GABA)浓度分别降至对照平均值的62%、45%和55%。GPi(144%)和ST(134%)中的谷氨酸浓度升高。胆碱乙酰转移酶(ChAT)活性在GPe(232%)、GPi(218%)、ST(161%)以及丘脑腹前核(VA,210%)和腹外侧核(VL,193%)中升高。GPe和GPi中的去甲肾上腺素(NA)浓度分别为对照平均值的56%和43%。多巴胺能和5-羟色胺能系统未显示出明显变化。网格微切割分析显示,3名对照者丘脑中GABA呈斑片状分布,而根据霍普夫图谱,成人起病的PPD中腹口核(VO)中一个富含GABA的小区域消失。这些结果有力地表明:(1)GP的GABA能神经元选择性退化,纹状体苍白球GABA能神经末梢活性降低;(2)GP、ST、VA和VL中的ChAT活性增加;(3)丘脑底核苍白球谷氨酸能系统活性未降低;(4)GP中去甲肾上腺素能系统活性降低;以及(5)人脑中丘脑的VO特异性接受来自GP的GABA能神经末梢。

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