Bjaalie J G
Exp Brain Res. 1985;57(3):585-97. doi: 10.1007/BF00237845.
Following large injections of horseradish peroxidase - wheat germ agglutinin in the pontine nuclei, corticopontine neurons in areas 18 and 19 were quantitatively mapped and flat maps showing the distribution of retrogradely labeled cells were constructed. The areal borders were defined either cyto- and myeloarchitectonically or from standard retinotopic maps presented in frontal sections (Tusa et al. 1981). Maps of the retinotopic organization in areas 18 and 19 (Tusa et al. 1979) were transferred to the present flat maps. Thus, the number and distribution of pontine projecting cells could be correlated with the retinotopic organization. The cell density (number of labeled cells per mm2 cortex) is in both areas highest in the cortex representing the lower and upper visual periphery and decreases towards the representation of the retinal central area. However, since in both areas 18 and 19 the visual field representation is twisted and portions of the visual field are magnified, the actual number of cells is higher in the cortex representing the central area and the lower medial visual field than in other parts. The cortex representing the lower hemifield contains approximately 2/3 (mean, N = 4) of the corticopontine cells in both areas. The average density of corticopontine cells increases from area 17 through 18 to 19, but the total number of cells within each of the areas is about the same (area 17: 18000 cells, area 18: 13400 cells, area 19: 17200 cells; mean, N = 4; data on area 17 from Bjaalie and Brodal, 1983). In conclusion, areas 17, 18 and 19 contribute about equally in quantitative terms to the pontine nuclei. Furthermore, assuming that the corticopontine neurons transmit spatially relevant information, there is a moderate overrepresentation of central vision and the lower medial visual field in the pontine projection from areas 18 and 19. This visual field representation is remarkably similar to that found in the corticopontine projection from area 17 (Bjaalie and Brodal 1983).
在脑桥核中大量注射辣根过氧化物酶 - 小麦胚凝集素后,对18区和19区的皮质脑桥神经元进行了定量定位,并构建了显示逆行标记细胞分布的平面图。区域边界通过细胞构筑和髓鞘构筑法定义,或根据额叶切片中呈现的标准视网膜拓扑图来确定(图萨等人,1981年)。18区和19区的视网膜拓扑组织图(图萨等人,1979年)被转移到当前的平面图上。因此,脑桥投射细胞的数量和分布可以与视网膜拓扑组织相关联。细胞密度(每平方毫米皮质中标记细胞的数量)在这两个区域中,在代表下部和上部视觉周边的皮质中最高,并向视网膜中央区域的代表部位降低。然而,由于在18区和19区中视野代表都是扭曲的,并且视野的部分区域被放大,因此在代表中央区域和下部内侧视野的皮质中,实际细胞数量比其他部位更高。代表下部视野的皮质在这两个区域中均包含约2/3(平均值,N = 4)的皮质脑桥细胞。皮质脑桥细胞的平均密度从17区经18区到19区逐渐增加,但每个区域内的细胞总数大致相同(17区:18000个细胞,18区:13400个细胞,19区:17200个细胞;平均值,N = 4;17区数据来自比亚利和布罗达尔,1983年)。总之,从数量上看,17区、18区和19区对脑桥核的贡献大致相等。此外,假设皮质脑桥神经元传递空间相关信息,在来自18区和19区的脑桥投射中,中央视觉和下部内侧视野存在适度的过度代表。这种视野代表与在来自17区的皮质脑桥投射中发现的非常相似(比亚利和布罗达尔,1983年)。