Giacomantonio Clare E, Goodhill Geoffrey J
Queensland Brain Institute, The University of Queensland, St Lucia, QLD, Australia.
J Neurosci. 2007 May 2;27(18):4935-46. doi: 10.1523/JNEUROSCI.1261-06.2007.
When blood vessels occlude the photoreceptor layer in the retina, they cast shadows onto the photoreceptors, creating angioscotomas (regions of the visual field to which that eye is blind). Remarkably, Adams and Horton (2002) have recently shown that it is sometimes possible to observe representations of these angioscotomas anatomically in the primary visual cortices of squirrel monkeys. However, there is substantial variability in the degree and form of these representations. The source of this variability is difficult to determine experimentally, because experimental studies are unavoidably limited by small sample size. In addition, experimental studies cannot compare the map structure that would develop with and without an angioscotoma. Here, we investigate these phenomena computationally using feature-mapping models of visual cortical development, which are not subject to the same limitations. These models suggest that the primary source of variability in angioscotoma representation is the precise timing of the onset of visual experience relative to the time course of ocular dominance column segregation. Furthermore, the models predict that angioscotomas could compete for control of local column layout with other influences such as cortical shape but that they have a small effect on the structure of orientation preference maps.
当血管阻塞视网膜中的光感受器层时,它们会在光感受器上投射阴影,形成血管性暗点(该眼失明的视野区域)。值得注意的是,亚当斯和霍顿(2002年)最近表明,有时可以在松鼠猴的初级视觉皮层中通过解剖学观察到这些血管性暗点的表征。然而,这些表征的程度和形式存在很大差异。这种变异性的来源很难通过实验确定,因为实验研究不可避免地受到小样本量的限制。此外,实验研究无法比较有和没有血管性暗点时会形成的图谱结构。在这里,我们使用视觉皮层发育的特征映射模型对这些现象进行计算研究,这些模型不受同样的限制。这些模型表明,血管性暗点表征变异性的主要来源是视觉经验开始的精确时间相对于眼优势柱分离的时间进程。此外,这些模型预测,血管性暗点可能会与其他影响因素(如皮层形状)竞争对局部柱布局的控制,但它们对方向偏好图谱的结构影响较小。