Vanni-Mercier G, Magnin M
Exp Brain Res. 1982;46(3):368-76. doi: 10.1007/BF00238631.
Single unit activity of 842 cells has been recorded in cat visual cortex and analyzed with respect to vestibular induced, and spontaneous saccadic eye movements performed in the dark. This study has been done in awake, chronically implanted cats, subsequently placed in "acute" conditions to achieve the precise retinotopic mapping of the cortical areas previously investigated. In areas 17 and 18, respectively, 27% and 24% of the cells tested were influenced by horizontal saccadic eye movements in the dark (E.M. cells). In the Clare-Bishop area, the proportion of E.M. cells was 12%, while only 2% of such cells were found in areas 19 and 21. The distribution of E.M. cells in areas 17 and 18 with respect to retinotopy showed that E.M. cells were more numerous in the cortical zones devoted to the representation of the area centralis (38% in area 17, 27% in area 18) than in the zones subserving the periphery of the visual field (17% and 12%, respectively). Two of the characteristics of E.M. cell activations appear dependent on the retinotopic organization. First, larger number of E.M. cells presenting an asymmetry in their responses to horizontal saccadic eye movements in opposite directions (directional E.M. cells) were encountered in the cortical representation of the peripheral visual field. 53% of E.M. cells recorded in area 17 and 71% in area 18 were directional in the cortex corresponding to the peripheral visual field. This percentage was of 23% and 25% respectively in the cortex devoted to area centralis. Second, E.M. cells were found to have a latency from the onset of the saccade systematically larger than 100 ms (i.e., they discharged at, or after the end of the eye movement) if they were located in the cortical representation of the area centralis, while E.M. cells related to the peripheral visual field displayed a wider range of latencies (0-240 ms). Results obtained in Clare Bishop area, although limited to the representation of the peripheral visual field, were quantitatively and qualitatively similar to those observed in the homologous retinotopic zones of areas 17 and 18. It is concluded that an extra-retinal input related to oculomotor activity is sent to the cat visual cortex and is organized, at least in areas 17 and 18, with respect to the retinotopic representation of the visual field. These data support the hypothesis of a functional duality between central and peripheral vision and are discussed in the context of visual-oculomotor integration.
在猫的视觉皮层中记录了842个细胞的单位活动,并针对前庭诱发的以及在黑暗中进行的自发性眼球跳动进行了分析。这项研究是在清醒的、长期植入电极的猫身上进行的,随后将其置于“急性”条件下,以实现对先前研究的皮层区域进行精确的视网膜定位映射。在17区和18区,分别有27%和24%的受试细胞受到黑暗中水平眼球跳动的影响(眼动细胞)。在克莱尔-毕晓普区,眼动细胞的比例为12%,而在19区和21区仅发现2%的此类细胞。17区和18区眼动细胞相对于视网膜定位的分布表明,在专门代表中央凹区域的皮层区域中,眼动细胞数量更多(17区为38%,18区为27%),而在服务于视野周边的区域中则较少(分别为17%和12%)。眼动细胞激活的两个特征似乎取决于视网膜定位组织。首先,在周边视野的皮层表征中,遇到更多对相反方向的水平眼球跳动反应不对称的眼动细胞(定向眼动细胞)。在17区记录的眼动细胞中有53%,在18区记录的眼动细胞中有71%在对应周边视野的皮层中是定向的。在专门代表中央凹区域 的皮层中,这一比例分别为23%和25%。其次,如果眼动细胞位于中央凹区域的皮层表征中,发现它们从眼球跳动开始的潜伏期系统性地大于100毫秒(即它们在眼球运动结束时或之后放电),而与周边视野相关的眼动细胞显示出更广泛的潜伏期范围(0 - 240毫秒)。在克莱尔 - 毕晓普区获得的结果,尽管仅限于周边视野的表征,但在数量和质量上与在17区和18区同源视网膜定位区域中观察到的结果相似。得出的结论是,与眼球运动活动相关的视网膜外输入被发送到猫的视觉皮层,并且至少在17区和18区,是根据视野的视网膜定位表征进行组织的。这些数据支持了中央视觉和周边视觉之间功能二元性的假设,并在视觉 - 眼球运动整合的背景下进行了讨论。