Insausti R, Tuñón T, Sobreviela T, Insausti A M, Gonzalo L M
Department of Anatomy, University of Navarra, Pamplona, Spain.
J Comp Neurol. 1995 May 1;355(2):171-98. doi: 10.1002/cne.903550203.
The entorhinal cortex of man is in the medial aspect of the temporal lobe. As in other mammalian species, it constitutes an essential component of the hippocampal formation and the route through which the neocortex interacts with the hippocampus. The importance of knowing its architecture in detail arises from the possibility of extrapolating it to experimental findings, notably in the nonhuman primate. We have investigated the cytoarchitectonic features of the human entorhinal cortex by using as a base our previous study (D.G. Amaral, R. Insausti, and W.M. Cowan [1987] J. Comp. Neurol. 264:326-355) of the nonhuman primate entorhinal cortex. We prepared serial sections of the temporal lobe from 35 normal brains. Thionin- and myelin-stained series were made of all cases. Sections spaced 500 microns apart through the full rostrocaudal extent of the entorhinal cortex were analyzed. The human entorhinal cortex is made up of six layers, of which layer IV does not appear throughout all subfields of the entorhinal cortex. The overall appearance resembles that of the adjacent neocortex in lateral and caudal portions. In harmony with general structural principles in the nonhuman primate entorhinal cortex, our analysis supports the partitioning of the human entorhinal cortex into eight different subfields. (1) The olfactory subfield (EO), the rostralmost field, is little laminated. (2) The lateral rostral subfield (ELr), laterally located, merges with the laterally adjacent perirhinal cortex. (3) The rostral subfield (ER) is between EO and ELr, with better differentiation of layers II and III than EO. (4) The medial intermediate subfield (EMI) is located at the medial border. (5) The intermediate field (EI) is a lateral continuation of EMI; lamina dissecans (layer IV) can be best appreciated in this field. (6) The lateral caudal subfield (ELc) laterally borders on EI as a continuation of ELr. (7) The caudal subfield (EC) lies caudal to the beginning of the hippocampal fissure, with a distinctive, clear space (Vc) between layers V and VI. (8) The caudal limiting field (ECL) forms the caudal termination of the entorhinal cortex. Thus our parcellation of the entorhinal cortex in man is largely parallel to that arrived at in the monkey. This close homology provides a rational basis for the application to clinical problems of anatomical and functional information obtained in experimental work in nonhuman primates.
人类的内嗅皮质位于颞叶内侧。与其他哺乳动物一样,它是海马结构的重要组成部分,也是新皮质与海马相互作用的途径。详细了解其结构的重要性在于有可能将其外推至实验结果,尤其是在非人类灵长类动物中。我们以之前对非人类灵长类动物内嗅皮质的研究(D.G. 阿马拉尔、R. 因绍斯蒂和W.M. 考恩 [1987]《比较神经学杂志》264:326 - 355)为基础,研究了人类内嗅皮质的细胞构筑特征。我们制备了35个正常大脑颞叶的连续切片。所有病例都制作了硫堇染色和髓鞘染色系列切片。对在内嗅皮质整个前后范围每隔500微米的切片进行了分析。人类内嗅皮质由六层组成,其中第四层在整个内嗅皮质的所有亚区并非都有。其整体外观在外侧和尾侧部分类似于相邻的新皮质。与非人类灵长类动物内嗅皮质的一般结构原则一致,我们的分析支持将人类内嗅皮质划分为八个不同的亚区。(1)嗅亚区(EO),最靠前的区域,几乎没有分层。(2)外侧吻侧亚区(ELr),位于外侧,与外侧相邻的嗅周皮质融合。(3)吻侧亚区(ER)在EO和ELr之间,其第二层和第三层比EO分化更好。(4)内侧中间亚区(EMI)位于内侧边界。(5)中间区(EI)是EMI的外侧延续;在这个区域可以最好地辨认出分离层(第四层)。(6)外侧尾侧亚区(ELc)作为ELr的延续,在外侧与EI相邻。(7)尾侧亚区(EC)位于海马裂起始部的尾侧,在第五层和第六层之间有一个独特的、清晰的间隙(Vc)。(8)尾侧界限区(ECL)构成内嗅皮质的尾侧终末。因此,我们对人类内嗅皮质的分区在很大程度上与在猴子中得出的分区平行。这种密切的同源性为将在非人类灵长类动物实验工作中获得的解剖学和功能信息应用于临床问题提供了合理的基础。