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猴子体感、运动及顶叶皮质中皮质构筑区的皮质内连接

Intracortical connectivity of architectonic fields in the somatic sensory, motor and parietal cortex of monkeys.

作者信息

Jones E G, Coulter J D, Hendry S H

出版信息

J Comp Neurol. 1978 Sep 15;181(2):291-347. doi: 10.1002/cne.901810206.

Abstract

Anterograde and retrograde transport methods were used to study the corticocortical connectivity of areas 3a, 3b, 1, 2, 5, 4 and 6 of the monkey cerebral cortex. Fields were identified by cytoarchitectonic features and by thalamic connectivity in the same brains. Area 3a was identified by first recording a short latency group I afferent evoked potential. Attempts were made to analyze the data in terms of: (1) routes whereby somatic sensory input might influence the performance of motor cortex neurons; (2) possible multiple representations of the body surface in the component fields of the first somatic sensory area (SI). Apart from vertical interlaminar connections, two types of intracortical connectivity are recognized. The first, regarded as "non-specific," consists of axons spreading out in layers I, III and V-VI from all sides of an injection of isotope; these cross architectonic borders indiscrimininately. They are not unique to the regions studied. The second is formed by axons entering the white matter and re-entering other fields. In these, they terminate in layers I-IV in one or more mediolaterally oriented strips of fairly constant width (0.5--1 mm) and separated by gaps of comparable size. Though there is a broadly systematic topography in these projections, the strips are probably best regarded as representing some feature other than receptive field position. Separate representations are nevertheless implied in area 3b, in areas 1 and 2 (together), in areas 3a and 4 (together) and in area 5; with, in each case, the representations of the digits pointed at the central sulcus. Area 3b is not connected with areas 3a or 4, but projects to a combined areas 1 and 2. Area 1 is reciprocally connected with area 3a and area 2 reciprocally with area 4. The connectivity of area 3a, as conventionally identified, is such that it is probably best regarded not as an entity, but as a part of area 4. Areas identified by others as area 3a should probably be regraded as parts of area 3b. Parts of area 5 that should be more properly considered as area 2, and other parts that receive thalamic input not from the ventrobasal complex but from the lateral nuclear complex and anterior pulvinar, are also interconnected with area 4. More posterior parts of area 5 are connected with laterally placed parts of area 6. A more medial part of area 6, the supplementary motor area, occupies a pivotal position in the sensory-motor cortex, for it receives fibers from areas 3a, 4, 1, 2 and 5 (all parts), and projects back to areas 3a, 4 and 5.

摘要

采用顺行和逆行运输方法研究了猴大脑皮质3a、3b、1、2、5、4和6区的皮质皮质连接性。在同一大脑中,通过细胞构筑特征和丘脑连接性来识别脑区。通过首先记录短潜伏期I类传入诱发电位来识别3a区。尝试从以下方面分析数据:(1)躯体感觉输入可能影响运动皮质神经元活动的途径;(2)第一躯体感觉区(SI)各组成区域中体表可能的多重表征。除了垂直的层间连接外,还识别出两种类型的皮质内连接。第一种被认为是“非特异性的”,由从同位素注射部位四周向I、III和V - VI层扩散的轴突组成;这些轴突随意跨越细胞构筑边界。它们并非所研究区域特有的。第二种由进入白质并重新进入其他区域的轴突形成。在这些区域中,它们终止于I - IV层中一个或多个宽度相当恒定(0.5 - 1毫米)且由大小相当的间隙分隔的、呈内外侧排列的条带中。尽管这些投射存在大致系统的拓扑结构,但这些条带可能最好被视为代表了除感受野位置之外的某些特征。然而,在3b区、1区和2区(合在一起)、3a区和4区(合在一起)以及5区中都暗示存在单独的表征;在每种情况下,手指的表征都指向中央沟。3b区与3a区或4区不相连,但投射到合并的1区和2区。1区与3a区相互连接,2区与4区相互连接。传统上所识别的3a区的连接性表明,它可能最好不被视为一个独立的实体,而应被视为4区的一部分。其他人所识别为3a区的区域可能应重新归类为3b区的一部分。5区中一些应更恰当地视为2区的部分,以及其他一些接受并非来自腹侧基底复合体而是来自外侧核复合体和前丘脑的丘脑输入的部分,也与4区相互连接。5区更靠后的部分与6区外侧的部分相连。6区更内侧的部分,即辅助运动区,在感觉运动皮质中占据关键位置,因为它接收来自3a、4、1、2和5区(所有部分)的纤维,并投射回3a区、4区和5区。

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