Stanton G B, Deng S Y, Goldberg M E, McMullen N T
Department of Anatomy, Howard University College of Medicine, Washington, D.C. 20059.
J Comp Neurol. 1989 Apr 15;282(3):415-27. doi: 10.1002/cne.902820308.
The cytoarchitecture of the prearcuate gyrus, including the region of the physiologically defined frontal eye fields (FEF), was studied in four macaque monkeys (Macaca fascicularis, M. mulatta) to determine if the FEF could be anatomically identified. Brain sections were stained with standard Nissl and, in some cases, myelin stains. Two nonstandard planes of section were used: one tangential to the prearcuate gyrus and the second normal to the most posterior bend of the prearcuate gyrus. The first plane of section was advantageous for studying the location of the FEF with reference to the entire medial-lateral extent of the gyrus and the second allowed good comparisons of the FEF to adjacent anterior and posterior cortical areas. Frontal plane sections through the prearcuate gyrus were also examined in 15 macaque monkeys for comparison with sections cut normal to the posterior bend of the gyrus and tangential to the gyrus. Intracortical microstimulation was performed in three monkeys. The FEF was defined as the area from which low-threshold (less than or equal to 50 microA) saccades could be evoked. The area extended about 10 mm along the anterior bank of the arcuate sulcus. Within the area, saccade amplitudes were represented in a mediolateral, large-to-small topography. No topography of saccade direction was noted within FEF but reversals of saccade direction for any given electrode pass were found. These results confirm the results from our earlier mapping study of FEF (Bruce et al.: J. Neurophysiol. 54:714-734, '85). Cell bodies of large pyramidal cells in layers III and V of the prearcuate gyri from three hemispheres were measured with the aid of an image-combining computer microscope. The distribution of cells of greater than 22 microns diameter or cross-sectional areas of greater than 500 microns 2 were plotted. In one monkey, marker lesions made at microstimulation sites within the FEF or in adjacent non-FEF areas were also plotted. The location of the FEF appeared to coincide with the concentration of large layer V pyramidal cells in the prearcuate gyrus rather than with any previously mapped cytoarchitectonic area. The numbers of large pyramids in layer V were noticeably reduced along the lip of the prearcuate gyrus and at dorsomedial and ventrolateral locations which were outside the physiologically defined FEF.
在四只猕猴(食蟹猴、恒河猴)中研究了弓状前回的细胞构筑,包括生理学上定义的额叶眼区(FEF)区域,以确定是否能从解剖学上识别FEF。脑切片用标准尼氏染色,在某些情况下还用髓鞘染色。使用了两个非标准的切片平面:一个与弓状前回相切,另一个与弓状前回最后端的弯曲处垂直。第一个切片平面有利于参照回的整个内外侧范围研究FEF的位置,第二个则便于将FEF与相邻的前后皮质区域进行良好比较。还检查了15只猕猴中通过弓状前回的额状面切片,以便与垂直于回的后弯处和与回相切处切割的切片进行比较。在三只猴子中进行了皮质内微刺激。FEF被定义为能诱发低阈值(小于或等于50微安)扫视的区域。该区域沿弓状沟的前缘延伸约10毫米。在该区域内,扫视幅度呈内外侧从大到小的地形图分布。在FEF内未观察到扫视方向的地形图,但在任何给定电极通道中发现了扫视方向的反转。这些结果证实了我们早期对FEF进行定位研究的结果(Bruce等人:《神经生理学杂志》54:714 - 734,'85)。借助图像合成计算机显微镜测量了来自三个半球的弓状前回第III层和第V层中大型锥体细胞的胞体。绘制了直径大于22微米或横截面积大于500平方微米的细胞分布。在一只猴子中,还绘制了在FEF内或相邻非FEF区域的微刺激部位所做的标记损伤。FEF的位置似乎与弓状前回中第V层大型锥体细胞的集中区域一致,而不是与任何先前绘制的细胞构筑区域一致。在弓状前回的边缘以及生理定义的FEF之外的背内侧和腹外侧位置,第V层大型锥体的数量明显减少。