Cortical responses to local electrical stimulation of retina.

Abstract Extensive cortical excitation from punctiform photic stimuli has been difficult to interpret because of intraoptic diffusion of light. Direct electrical stimulation of the exposed retina was thus used in this attempt to determine the degree of spatial elaboration of stimuli in the retinocortical system. Multichannel CRO recording from cortex and optic tract show two types of response in anesthetized or “midpontine” animals. The “early” response is identical in form to potentials elicited by optic tract stimuli, but has a latency of 2 to 5.3 msec, depending upon distance of intraretinal conduction. Constancy of timing in the cortical spike sequence despite varying arrival latencies shows that this well-known series of spikes is not generated as a consequence of conduction velocity differences in optic nerve fibers. Early potentials can be highly restricted in cortical location and, save for their predominance in the lateral dorsal region of marginal gyrus, generally conform in distribution to Talbot and Marshall's scheme of retinocortical topographical relations. “Late” responses are complex, but most are similar to photically elicited responses in form and latency. Their threshold is usually lower than that for early responses. Their cortical distribution for a given retinal locus greatly exceeds that of the early response, sometimes including ipsilateral cortex even to stimulation of nasal retina.Since optic tract potentials continue for over 100 msec after the 1-msec retinal pulse, it is possible that some of the spatial elaboration of the late response occurs in the retina.

[1]  M. Clare,et al.  Sites of origin of electric potentials in striate cortex. , 1952, Journal of neurophysiology.

[2]  Hsiang-Tung Chang,et al.  An analysis of primary response of visual cortex to optic nerve stimulation in cats. , 1950, Journal of neurophysiology.

[3]  R. Doty,et al.  Functional Significance of the Topographical Aspects of the Retino-Cortical Projection , 1961 .

[4]  Ueber die Sehrinde (Area striata) und ihre Beziehungen zu den primären optischen Zentren. , 1914 .

[5]  S. A. Talbot,et al.  Physiological Studies on Neural Mechanisms of Visual Localization and Discrimination , 1941 .

[6]  M. Clare,et al.  A note on the characteristic response pattern in primary sensory projection cortex of the cat following a synchronous afferent volley. , 1956, Electroencephalography and clinical neurophysiology.

[7]  R. Doty,et al.  Potentials evoked in cat cerebral cortex by diffuse and by punctiform photic stimuli. , 1958, Journal of neurophysiology.

[8]  E. Evarts,et al.  Multiple response to photic stimulation in cats. , 1959, The American journal of physiology.

[9]  H. T. Chang Functional organization of central visual pathways. , 1952, Research publications - Association for Research in Nervous and Mental Disease.

[10]  G. Moruzzi,et al.  Effects of complete pontine transections on the sleep-wakefulness rhythm: the midpontine pretrigeminal preparation , 1959 .

[11]  E. Dodt,et al.  [Nerve conduction velocity in the retina]. , 1956, Experientia.

[12]  Chang Ht Functional organization of central visual pathways. , 1952 .

[13]  H. Jasper,et al.  A stereotaxic atlas of the diencephalon of the cat , 1960 .

[14]  K. Motokawa,et al.  Interaction of slow potentials of the retina evoked by photic and electric stimuli. , 1959, The Tohoku journal of experimental medicine.