Tootell R B, Hamilton S L
Department of Psychology, University of California, Berkeley 94720.
J Neurosci. 1989 Aug;9(8):2620-44. doi: 10.1523/JNEUROSCI.09-08-02620.1989.
To study the functional organization of secondary visual cortex (V2) in the primate, 14C-2-deoxy-d-glucose (DG) was injected while macaque monkeys were shown specific visual stimuli. Wherever possible, patterns of DG uptake were compared with the position of dark and light cytochrome oxidase (cytox) stripes (Tootell et al., 1983). Often, the DG effects of 2 different stimuli were compared in the same hemisphere to eliminate ambiguities inherent in between-animal comparisons. Data were obtained from a large number of animals in conjunction with related DG studies in area V1 (primary visual or striate cortex). The following conclusions were reached: (1) in some macaque monkeys, dark cytox stripes were faint or absent. Although this could conceivably be due to poor staining technique, some evidence suggests that the lack of enzyme stripe pattern is real. In all animals, including those that showed poor or no cytox staining evidence for stripes, the functional architecture revealed by the DG was consistently present and robust. (2) Uniform gray stimuli produce a relatively uniform pattern and minimal stimulus-related DG uptake. (3) Eye movements per se produce some uptake in the V2 stripes. (4) Very generalized visual stimulation conditions (e.g., binocular stimulation with a grating of varied orientation and varied spatial frequency) produced a pattern of uptake that is greatest in both sets of dark cytox stripes and lighter in the light cytochrome stripes. (5) In both the DG and cytox results, the V2 "stripes" are more accurately described as stripe-shaped collections of patches. (6) In almost all cases, DG patterns were columnar in shape, extending from white matter to cortical surface. The boundaries of the columns were most sharply defined, and the contrast was highest, in layers 3B/4, becoming slightly more blurry and lower in contrast in other layers. Laminar differences between DG patterns in V2 were almost negligible, compared with the profound laminar differences in macaque V1. (7) There is no DG evidence for, and much against, the possibility of an ocular dominance architecture in V2. (8) There are orientation columns in macaque V2. DG-labeled orientation columns are spaced further apart than those in V1, by a factor of about 1.6, but the columns are not correspondingly wider. (9) Spatially diffuse variations in color produce high uptake confined, at least largely, to the thin cytox stripes. (10) There is evidence for spatially antagonistic color surrounds in color cells in the thin stripes.(ABSTRACT TRUNCATED AT 400 WORDS)
为研究灵长类动物次级视皮层(V2)的功能组织,在向猕猴呈现特定视觉刺激时注射了14C-2-脱氧-D-葡萄糖(DG)。只要有可能,就将DG摄取模式与暗、亮细胞色素氧化酶(细胞色素氧化酶)条带的位置进行比较(Tootell等人,1983年)。通常,在同一半球比较两种不同刺激的DG效应,以消除动物间比较中固有的模糊性。数据来自大量动物,并结合V1区(初级视皮层或纹状皮层)的相关DG研究。得出以下结论:(1)在一些猕猴中,暗细胞色素氧化酶条带微弱或缺失。尽管这可能是由于染色技术不佳,但一些证据表明酶条带模式的缺失是真实的。在所有动物中,包括那些细胞色素氧化酶染色显示条带不佳或无条带证据的动物,DG揭示的功能结构始终存在且清晰。(2)均匀的灰色刺激产生相对均匀的模式和与刺激相关的最小DG摄取。(3)眼球运动本身在V2条带中产生一些摄取。(4)非常普遍的视觉刺激条件(例如,用不同方向和不同空间频率的光栅进行双眼刺激)产生的摄取模式在两组暗细胞色素氧化酶条带中最大,在亮细胞色素条带中较浅。(5)在DG和细胞色素氧化酶的结果中,V2“条带”更准确地描述为斑块状的条带集合。(6)几乎在所有情况下,DG模式呈柱状,从白质延伸至皮层表面。柱的边界在3B/4层定义最清晰,对比度最高,在其他层变得稍模糊且对比度较低。与猕猴V1中显著的层间差异相比,V2中DG模式的层间差异几乎可以忽略不计。(7)没有DG证据支持V2中存在眼优势结构,且有很多证据反对这种可能性。(8)猕猴V2中有方向柱。DG标记的方向柱比V1中的间隔更远,约为1.6倍,但柱的宽度并没有相应变宽。(9)颜色在空间上的漫反射变化产生的高摄取至少在很大程度上限于薄的细胞色素氧化酶条带。(10)有证据表明薄条带中的颜色细胞存在空间拮抗的颜色周边。(摘要截断于400字)