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正常和蹒跚突变小鼠小脑核的定量形态学分析。I. 形态学和细胞数量。

Quantitative morphological analysis of the cerebellar nuclei in normal and lurcher mutant mice. I. Morphology and cell number.

作者信息

Heckroth J A

机构信息

Indiana University School of Medicine, Terre Haute Center for Medical Education at Indiana State University 47809.

出版信息

J Comp Neurol. 1994 May 1;343(1):173-82. doi: 10.1002/cne.903430113.

Abstract

The present study indicates that the cerebellar nuclei of the mouse are essentially identical in structure with those described in the rat, and that the atrophic cerebellar nuclei in lurcher mutant mice exhibit a comparable anatomical organization. A quantitative estimate of the atrophy observed in the cerebellar nuclei of the adult lurcher mutant mouse reveals an overall 60% decrease in volume. Cell counts in the wild-type cerebellar nuclei reveal a total of 8,528 principal neurons and 10,203 small neurons. The ratio of small/principal neurons is 0.5 in the fastigial nucleus and between 1 and 1.5 in other subdivisions. In lurcher, the principal neurons are slightly reduced in number (-20%) in the nuclear complex, while the population of small neurons is reduced by 37% in the interposed and dentate nuclei, but is unchanged in the fastigial nucleus. These results suggest that the massive deafferentation of the cerebellar nuclei that occurs between 10 and 30 days of age in lurcher mutants has a relatively mild effect on the principal cerebellar nuclear neurons. In the population of small neurons, however, the effect of deafferentation may be exacerbated by a secondary retrograde transneuronal degeneration brought on by the severe degeneration of inferior olivary neurons and cerebellar cortex in this mutant.

摘要

本研究表明,小鼠的小脑核在结构上与大鼠中所描述的基本相同,并且蹒跚突变小鼠中萎缩的小脑核呈现出类似的解剖结构。对成年蹒跚突变小鼠小脑核中观察到的萎缩进行定量估计,结果显示总体积减少了60%。野生型小脑核中的细胞计数显示共有8528个主要神经元和10203个小神经元。顶核中小神经元/主要神经元的比例为0.5,在其他亚区中该比例在1到1.5之间。在蹒跚突变小鼠中,核复合体中的主要神经元数量略有减少(-20%),而在间位核和齿状核中,小神经元群体减少了37%,但在顶核中没有变化。这些结果表明,在蹒跚突变小鼠10至30日龄期间发生的小脑核大量传入神经阻滞对小脑核主要神经元的影响相对较小。然而,在小神经元群体中,由于该突变体中橄榄下核神经元和小脑皮质的严重退化所引发的继发性逆行跨神经元变性,传入神经阻滞的影响可能会加剧。

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