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进行性核上性麻痹中神经递质受体和神经递质转运体的改变。

Alterations of neurotransmitter receptors and neurotransmitter transporters in progressive supranuclear palsy.

作者信息

Landwehrmeyer B, Palacios J M

机构信息

Department of Pathology, University of Basel, Switzerland.

出版信息

J Neural Transm Suppl. 1994;42:229-46. doi: 10.1007/978-3-7091-6641-3_18.

DOI:10.1007/978-3-7091-6641-3_18
PMID:7525868
Abstract

Neurotransmitter receptors and neurotransmitter transporters were studied postmortem in the brains of 9 PSP patients by receptor autoradiography. Densities of dopamine uptake sites and neurotensin receptors were significantly reduced in striatum and substantia nigra consistent with a localization of these binding sites on degenerating dopaminergic nigrostriatal projection neurons. The densities of dopamine D1 receptors were unchanged. Dopamine D2 receptors were unaltered when labeled by [125I]-Iodosulpride or [3H]-CV 205 502, but appeared to be significantly reduced when labeled by [3H]-spiperone. Levels of D2 mRNA were comparable to control levels, suggesting that only subtypes of Dopamine D2-like receptors may be affected in PSP. Serotonin (5-HT) uptake sites and 5-HT receptors were not altered. The density of muscarinic receptors was reduced in striatum, possibly related to a degeneration of cholinergic striatal interneurons, but increased in internal globus pallidus. GABAA/BZ receptor binding sites were significantly reduced in both segments of globus pallidus, probably as a consequence of severe degeneration of intrinsic pallidal neurons in PSP. Binding of substance P in striatum tended to be decreased but failed to reach statistical significance. Compared to Parkinson's disease, the densities of more neurotransmitter receptors were altered in PSP. With the exception of increased muscarinic receptor binding sites in medial globus pallidus, the alterations seen in PSP seem to reflect cell loss rather than functional changes.

摘要

通过受体放射自显影技术,对9例进行性核上性麻痹(PSP)患者死后的大脑进行了神经递质受体和神经递质转运体的研究。纹状体和黑质中多巴胺摄取位点和神经降压素受体的密度显著降低,这与这些结合位点定位于退化的多巴胺能黑质纹状体投射神经元上一致。多巴胺D1受体的密度未发生变化。当用[125I] - 碘舒必利或[3H] - CV 205 502标记时,多巴胺D2受体未改变,但在用[3H] - 螺哌隆标记时似乎显著降低。D2 mRNA水平与对照水平相当,表明在PSP中可能仅多巴胺D2样受体的亚型受到影响。5-羟色胺(5-HT)摄取位点和5-HT受体未改变。纹状体中毒蕈碱受体的密度降低,可能与胆碱能纹状体中间神经元的退化有关,但在内侧苍白球中增加。苍白球两个节段中的GABAA/BZ受体结合位点均显著降低,这可能是PSP中苍白球固有神经元严重退化的结果。纹状体中P物质的结合倾向于降低,但未达到统计学意义。与帕金森病相比,PSP中有更多神经递质受体的密度发生改变。除了内侧苍白球中毒蕈碱受体结合位点增加外,PSP中观察到的改变似乎反映了细胞丢失而非功能变化。

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