Institute of Behavioural Neuroscience, Department of Experimental Psychology, University College London, London WC1H 0AP, UK; Max Planck Institute for Biological Cybernetics, 72076 Tuebingen, Germany.
Max Planck Institute for Biological Cybernetics, 72076 Tuebingen, Germany; Bio-Imaging Lab, University of Antwerp, 2610 Wilrijk, Belgium; Bernstein Center for Computational Neuroscience, 72076 Tuebingen, Germany.
Neuroimage. 2019 Apr 15;190:254-268. doi: 10.1016/j.neuroimage.2018.03.062. Epub 2018 Apr 6.
Damage to the primary visual cortex (V1) leads to a visual field loss (scotoma) in the retinotopically corresponding part of the visual field. Nonetheless, a small amount of residual visual sensitivity persists within the blind field. This residual capacity has been linked to activity observed in the middle temporal area complex (V5/MT+). However, it remains unknown whether the organization of hV5/MT+ changes following early visual cortical lesions. We studied the organization of area hV5/MT+ of five patients with dense homonymous defects in a quadrant of the visual field as a result of partial V1+ or optic radiation lesions. To do so, we developed a new method, which models the boundaries of population receptive fields directly from the BOLD signal of each voxel in the visual cortex. We found responses in hV5/MT+ arising inside the scotoma for all patients and identified two possible sources of activation: 1) responses might originate from partially lesioned parts of area V1 corresponding to the scotoma, and 2) responses can also originate independent of area V1 input suggesting the existence of functional V1-bypassing pathways. Apparently, visually driven activity observed in hV5/MT+ is not sufficient to mediate conscious vision. More surprisingly, visually driven activity in corresponding regions of V1 and early extrastriate areas including hV5/MT+ did not guarantee visual perception in the group of patients with post-geniculate lesions that we examined. This suggests that the fine coordination of visual activity patterns across visual areas may be an important determinant of whether visual perception persists following visual cortical lesions.
初级视皮层(V1)损伤会导致视野中与视网膜对应部分的视野丧失(盲点)。尽管如此,在盲区内仍存在少量残余视觉敏感度。这种残余能力与中颞区复合体(V5/MT+)中观察到的活动有关。然而,尚不清楚 V1 早期损伤后 hV5/MT+ 的组织是否发生变化。我们研究了 5 名患者的 hV5/MT+组织,这些患者由于 V1+或视辐射的部分损伤,导致视野的一个象限出现密集的同侧缺陷。为此,我们开发了一种新方法,该方法直接从视觉皮层每个体素的 BOLD 信号中对群体感受野的边界进行建模。我们发现所有患者的 hV5/MT+中都出现了盲点内的反应,并确定了两种可能的激活源:1)反应可能源于对应于盲点的 V1 部分损伤区域,以及 2)反应也可以独立于 V1 输入起源,表明存在功能上的 V1 旁路途径。显然,hV5/MT+中观察到的视觉驱动活动不足以介导有意识的视觉。更令人惊讶的是,包括 hV5/MT+在内的 V1 和早期外纹状区中与视觉相关的活动并不能保证我们检查的后神经节损伤患者组中的视觉感知。这表明视觉区域之间视觉活动模式的精细协调可能是视觉皮层损伤后视觉感知是否持续的重要决定因素。