Changes in the dorsal lateral geniculate nucleus of the squirrel monkey after unilateral ablation of the visual cortex

1972 ◽  
Vol 146 (4) ◽  
pp. 519-547 ◽  
Author(s):  
Margaret T. T. Wong-Riley
1996 ◽  
Vol 13 (5) ◽  
pp. 805-816 ◽  
Author(s):  
Bertram R. Payne ◽  
Stephen G. Lomber

AbstractThe purpose of the present study was to assess changes in the levels of cytochrome oxidase (CO) activity in the dorsal lateral geniculate nucleus (dLGN) of the adult cat following removal of primary visual cortical areas 17 and 18 on the day of birth (P1), P28, or in adulthood (≫6 months). Cytochrome oxidase activity was measured in histological sections 9 or more months after the cortical ablation. Control measures obtained from intact cats show that CO activity is normally highest in the A-laminae of dLGN, and slightly lower in the C-complex. Following visual cortex ablations incurred at any age, CO activity levels are reduced in the A-laminae. This reduction is most profound following ablations incurred on P28 or in adulthood. In contrast, CO activity in the C-complex of dLGN is at nearly normal levels following ablations on P1 or P28, but not in adulthood. These findings contribute to our understanding of the role played by the dLGN in the transfer of visual signals along retino-geniculo-extrastriate pathways that expand following early removal of areas 17 and 18. Moreover, they have implications for our understanding of spared behavioral functions attributed to the extrastriate cortex in cats which incurred early damage of areas 17 and 18.


1996 ◽  
Vol 13 (6) ◽  
pp. 1129-1142 ◽  
Author(s):  
James R. Wilson ◽  
Donna M. Forestner ◽  
Ryan P. Cramer

AbstractThree interneurons were recorded from and then injected with horseradish peroxidase in the parvocellular laminae of the squirrel monkey's (Saimiri sciureus) dorsal lateral geniculate nucleus. They were then examined using the electron microscope for their synaptic contacts, both the afferent contacts onto their dendrites and their presynaptic dendritic contacts onto presumptive projection (relay) neuron dendrites. The somata of these interneurons were small (mean = 178 μm2), but the dendritic trees were large compared with those of projection neurons. All three interneurons had similar synaptic patterns onto their dendrites with about equal numbers of retinal, cortical, and GABAergic contacts. The distribution of these contacts was more uniform compared with the same types of contacts made onto projection neurons. The presynaptic dendrites were observed to contact only the dendrites of presumptive projection neurons, and these contacts were nearly all in the form of geniculate triads. None of the three interneurons displayed an axon. The receptive fields of these interneurons were similar to those of projection cells, but were larger and had center-response signs that were the opposite of the projection neurons around them (e.g. OFF center for the dorsal part of the parvocellular mass where ON-center projection neurons reside). The squirrel monkey data provides additional evidence that one aspect of the laminar pattern observed in the parvocellular pathway of the primate's dLGN might be related to a segregation of projection neurons of one center-response sign with interneurons of the opposite center-response sign.


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