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人类小脑的黑质神经元(小脑色素核)及猴子中的同源物。

The melanoneurons of the human cerebellum (nucleus pigmentosus cerebellaris) and homologues in the monkey.

作者信息

Cowen D

出版信息

J Neuropathol Exp Neurol. 1986 May;45(3):205-21.

PMID:3958755
Abstract

Little has been written about the cells here termed cerebellar melanoneurons. This paper describes and illustrates their cytologic features and topographic relationships. In the human brain these large pigmented neurons are scattered in a narrow layer near the lateral wall, dorsal angle and roof of the fourth ventricle. They form an inconspicuous part (group A4) of the system of catecholamine, neuromelanin-containing cells well known in the brain stem. Rostrally, a few of them provide a tenuous continuity with the locus ceruleus but topographically the two nuclei are independent. With ordinary stains the cerebellar cells can be seen as early as the 26th week of gestation (the earliest period examined). Brown neuromelanin granules do not appear until two and a half years of age but argentaffin granules, foreshadowing the production of pigment, are found in increasing numbers in the fetal and postnatal period. Homologues of the human cerebellar cells are reported in two species of monkey, Macaca nemestrina and Lagothrix sp. Neuromelanin, not previously observed in non-human cerebellar cells, occurs in M. mulatta and M. nemestrina. The proximity of the cerebellar melanoneurons to the ventricle raises the possibility that they are related to functions of the ependyma, or that they influence, or are affected by, constituents of the cerebrospinal fluid. The pathologic changes they undergo in Parkinson's disease and other disorders are to be described elsewhere.

摘要

关于此处所称的小脑黑素神经元,相关著述甚少。本文描述并阐述了它们的细胞学特征及局部解剖关系。在人类大脑中,这些大型色素神经元散在于第四脑室侧壁、背角和顶部附近的一个狭窄层中。它们构成了脑干中熟知的含儿茶酚胺、神经黑素细胞系统中一个不显眼的部分(A4组)。在头侧,其中一些神经元与蓝斑有微弱的连续性,但在局部解剖学上,这两个核是独立的。用普通染色法,早在妊娠第26周(所检查的最早时期)就能看到小脑细胞。棕色神经黑素颗粒直到两岁半才出现,但嗜银颗粒在胎儿期和出生后数量不断增加,预示着色素的产生。在两种猴子,即豚尾猕猴和绒毛蛛猴中发现了人类小脑细胞的同源物。在恒河猴和豚尾猕猴中出现了以前在非人类小脑细胞中未观察到的神经黑素。小脑黑素神经元与脑室的接近增加了它们与室管膜功能相关的可能性,或者它们影响脑脊液成分或受其影响的可能性。它们在帕金森病和其他疾病中所经历的病理变化将在其他地方描述。

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