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使用多种现代神经解剖学和病理学标记物揭示的人类边缘后皮质的边界、范围和形态。

Borders, extent, and topography of human perirhinal cortex as revealed using multiple modern neuroanatomical and pathological markers.

机构信息

Department of Anatomy and Cell Biology, University of Iowa College of Medicine, Iowa City, Iowa, USA.

出版信息

Hum Brain Mapp. 2010 Sep;31(9):1359-79. doi: 10.1002/hbm.20940.

Abstract

Despite rapidly increasing interests in specific contributions of different components of human medial temporal lobe (MTL) to memory and memory impairments in normal aging and in many abnormal conditions such as Alzheimer's disease and Pick's disease, few modern neuroanatomical studies are available about the borders, extent, and topography of human perirhinal areas 35 and 36, which are important components of the MTL memory system. By a combined use of several cellular, neurochemical, and pathological markers, which mainly include neuronal nuclear antigen, calcium-binding proteins (parvalbumin and calbindin-D28k), nonphosphorylated neurofilament protein (SMI-32), Wisteria floribunda agglutinin, and abnormally phosphorylated tau (AT8), this study has revealed that the borders of human perirhinal areas 35 and 36 are significantly different from those defined with conventional Nissl staining. In general, areas 35 and 36 occupy the ventromedial temporopolar and rhinal sulcal regions, the collateral sulcal region, and the anterior two-thirds of fusiform gyrus or occipitotemporal gyrus. Furthermore, the precise borders, extent, and topography of human areas 35 and 36 and adjoining entorhinal cortex were marked at different anteroposterior levels of the MTL with reference to variations of rhinal and collateral sulci and other useful landmarks. These findings would provide reliable neuroanatomical base for the great and yet rapidly increasing number of neuroimaging studies of the human MTL structures in healthy and many abnormal conditions.

摘要

尽管人们对人类内侧颞叶(MTL)不同成分对正常衰老和许多异常情况(如阿尔茨海默病和皮克病)中的记忆和记忆障碍的特定贡献越来越感兴趣,但关于人类边缘区 35 和 36 的边界、范围和拓扑结构的现代神经解剖学研究却很少。这些区域是 MTL 记忆系统的重要组成部分。通过联合使用几种细胞、神经化学和病理标志物,主要包括神经元核抗原、钙结合蛋白(副钙蛋白和钙结合蛋白-D28k)、非磷酸化神经丝蛋白(SMI-32)、Wisteria floribunda 凝集素和异常磷酸化的 tau(AT8),本研究表明人类边缘区 35 和 36 的边界与传统的尼氏染色定义的边界有显著差异。一般来说,35 和 36 区占据了腹内侧颞极和鼻沟回区、侧副沟区以及梭状回或枕颞回的前 2/3。此外,还参照了鼻沟回和侧副沟以及其他有用的标志,在 MTL 的不同前后水平上标记了人类 35 和 36 区以及相邻的内嗅皮质的精确边界、范围和拓扑结构。这些发现将为健康和许多异常情况下人类 MTL 结构的大量且快速增加的神经影像学研究提供可靠的神经解剖学基础。

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