Role of cortico-cortical connections in mediating cerebral cortex plasticity: visual cortex model

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In mammals injury to the retina not only affects the neurones within the eye but also induces changes in the other parts of the brain, particularly in the visual cortex. It has been found that after retinal injury cells in the visual cortex, normally receiving an input from the injured part of the retina, now receive an input from adjacent normal retina ( ectopic receptive field ). All mammals with well developed vision have a large number of separate visual cortical areas (more than 30 in primates). These areas are arranged in a hierarchy in which it is thought that as features of the visual stimuli become more complex they are discriminated in the areas higher in the hierarchy. These higher-order areas also project back to lower-order areas. This feedback activity from the higher areas can be reversibly abolished by cooling a given area to about 10oC and then rewarming it back to its normal temperature. We will try to determine if in cats (animals with well developed vision) following damage to a small region of the retina the feedback activity from higher visual cortical areas affects the ectopic receptive fields in the lower visual cortical areas. Another possibility is that the ectopic receptive field apparent following retinal damage might depend on horizontal connections within the particular cortical area, running from normal cortex to the area of cortex affected by the lesion. We propose to test this idea by blocking reversibly (with chemical agents) transmission of these horizontal fibres and determining the characteristics of neurones in the area affected by the lesion. Understanding the role of feedback and horizontal cortico-cortical connections in establishing new ectopic receptive fields following spatially delineated damage to the retina will help us to understand the mechanisms underlying perceptual distortions and visual hallucinations which occur following retinal traumas or some age-related retinal degenerations.