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在先天性无胼胝体小鼠大脑中所见的走行于普罗布斯特纵束内的纤维:辣根过氧化物酶技术研究

The fibers which course within the Probst's longitudinal bundle seen in the brain of a congenitally acallosal mouse: a study with the horseradish peroxidase technique.

作者信息

Ozaki H S, Shimada M

机构信息

Department of Anatomy, Kagawa Medical School, Japan.

出版信息

Brain Res. 1988 Feb 16;441(1-2):5-14. doi: 10.1016/0006-8993(88)91377-7.

Abstract

The congenital absence of the corpus callosum, a brain anomaly frequently noted in humans, has been recently found to occur in some mice of the ddN strain in our laboratory. In the brains of these mice, the Probst's longitudinal bundle is always present on both cerebral hemispheres. In this research, the neuroanatomical features of the constituent fibers of this bundle were studied by iontophoretical injections of horseradish peroxidase into different loci in the neocortex of acallosal mouse brains. The results revealed that (1) certain cortical fibers of the Probst's bundle terminate in the ipsilateral neocortex; (2) some commissural fibers in the longitudinal bundle originate from the cells in the wide neocortical regions, and project to the opposite hemisphere in homotopic as well as heterotopic regions over the ventral hippocampal commissure; (3) the fibers from different cortical regions are arranged in a topographic manner within this bundle. The present data clearly demonstrate that a good portion of fibers in the Probst's longitudinal bundle seen in the congenitally acallosal mouse brain are corticocortical in nature, which indicates that this bundle has an ipsilateral neocortical association function.

摘要

胼胝体先天性缺失是人类中经常发现的一种脑异常,最近在我们实验室的一些ddN品系小鼠中也被发现。在这些小鼠的大脑中,普罗布斯特氏纵束在两个大脑半球上总是存在。在本研究中,通过将辣根过氧化物酶离子电渗注入无胼胝体小鼠大脑新皮质的不同位点,研究了该束组成纤维的神经解剖学特征。结果显示:(1)普罗布斯特氏束的某些皮质纤维终止于同侧新皮质;(2)纵束中的一些连合纤维起源于广泛的新皮质区域的细胞,并通过腹侧海马连合投射到对侧半球的同位和异位区域;(3)来自不同皮质区域的纤维在该束内以拓扑方式排列。目前的数据清楚地表明,在先天性无胼胝体小鼠大脑中看到的普罗布斯特氏纵束中的很大一部分纤维本质上是皮质-皮质的,这表明该束具有同侧新皮质联合功能。

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