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本文引用的文献

1
Parcellation of human temporal polar cortex: a combined analysis of multiple cytoarchitectonic, chemoarchitectonic, and pathological markers.人类颞极皮质的分区:多种细胞构筑、化学构筑和病理标记物的联合分析
J Comp Neurol. 2009 Jun 20;514(6):595-623. doi: 10.1002/cne.22053.
2
Recognition memory and the medial temporal lobe: a new perspective.识别记忆与内侧颞叶:一个新视角。
Nat Rev Neurosci. 2007 Nov;8(11):872-83. doi: 10.1038/nrn2154.
3
An MRI-based method for measuring volume, thickness and surface area of entorhinal, perirhinal, and posterior parahippocampal cortex.一种基于磁共振成像的测量内嗅皮质、嗅周皮质和海马旁后皮质体积、厚度及表面积的方法。
Neurobiol Aging. 2009 Mar;30(3):420-31. doi: 10.1016/j.neurobiolaging.2007.07.023. Epub 2007 Sep 11.
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Cytoarchitectonic and chemoarchitectonic subdivisions of the perirhinal and parahippocampal cortices in macaque monkeys.猕猴大脑梨状叶周围皮质和海马旁回皮质的细胞构筑和化学构筑分区
J Comp Neurol. 2007 Feb 20;500(6):973-1006. doi: 10.1002/cne.21141.
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Perirhinal cortex and its neighbours in the medial temporal lobe: contributions to memory and perception.内嗅皮质及其在内侧颞叶的相邻区域:对记忆和感知的贡献。
Q J Exp Psychol B. 2005 Jul-Oct;58(3-4):378-96. doi: 10.1080/02724990544000077.
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The contribution of the human medial temporal lobe to perception: bridging the gap between animal and human studies.人类内侧颞叶对感知的贡献:弥合动物研究与人类研究之间的差距。
Q J Exp Psychol B. 2005 Jul-Oct;58(3-4):300-25. doi: 10.1080/02724990444000168.
7
The role of the perirhinal cortex and hippocampus in learning, memory, and perception.嗅周皮质和海马体在学习、记忆及感知中的作用。
Q J Exp Psychol B. 2005 Jul-Oct;58(3-4):246-68. doi: 10.1080/02724990444000186.
8
The human perirhinal cortex and semantic memory.人类嗅周皮质与语义记忆。
Eur J Neurosci. 2004 Nov;20(9):2441-6. doi: 10.1111/j.1460-9568.2004.03710.x.
9
Quantifying medial temporal lobe damage in memory-impaired patients.量化记忆受损患者的内侧颞叶损伤。
Hippocampus. 2005;15(1):79-85. doi: 10.1002/hipo.20032.
10
Medial temporal lobe activation during encoding and retrieval of novel face-name pairs.在新面孔-名字对的编码和检索过程中内侧颞叶的激活。
Hippocampus. 2004;14(7):919-30. doi: 10.1002/hipo.20014.

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.

DOI:10.1002/hbm.20940
PMID:20082329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6870967/
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。