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J Neurophysiol 95: 3311-3327, 2006. First published January 25, 2006; doi:10.1152/jn.01168.2005
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TRANSLATIONAL PHYSIOLOGY

Electrical Stimulation of Mammalian Retinal Ganglion Cells With Multielectrode Arrays

Chris Sekirnjak1, Pawel Hottowy2, Alexander Sher3, Wladyslaw Dabrowski2, A. M. Litke3 and E. J. Chichilnisky1

1The Salk Institute for Biological Studies, San Diego, California; 2Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Krakow, Poland; and 3University of California, Santa Cruz, California

Submitted 4 November 2005; accepted in final form 22 January 2006

Existing epiretinal implants for the blind are designed to electrically stimulate large groups of surviving retinal neurons using a small number of electrodes with diameters of several hundred micrometers. To increase the spatial resolution of artificial sight, electrodes much smaller than those currently in use are desirable. In this study, we stimulated and recorded ganglion cells in isolated pieces of rat, guinea pig, and monkey retina. We used microfabricated hexagonal arrays of 61 platinum disk electrodes with diameters between 6 and 25 µm, spaced 60 µm apart. Charge-balanced current pulses evoked one or two spikes at latencies as short as 0.2 ms, and typically only one or a few recorded ganglion cells were stimulated. Application of several synaptic blockers did not abolish the evoked responses, implying direct activation of ganglion cells. Threshold charge densities were typically <0.1 mC/cm2 for a pulse duration of 100 µs, corresponding to charge thresholds of <100 pC. Stimulation remained effective after several hours and at high frequencies. To show that closely spaced electrodes can elicit independent ganglion cell responses, we used the multielectrode array to stimulate several nearby ganglion cells simultaneously. From these data, we conclude that electrical stimulation of mammalian retina with small-diameter electrode arrays is achievable and can provide high temporal and spatial precision at low charge densities. We review previous epiretinal stimulation studies and discuss our results in the context of 32 other publications, comparing threshold parameters and safety limits.


Address for reprint requests and other correspondence: E. J. Chichilnisky, The Salk Institute for Biological Studies, 10010 N. Torrey Pines Rd., La Jolla, CA 92037 (E-mail: ej{at}salk.edu)




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