Activation of ganglion cells and axon bundles using epiretinal electrical stimulation

Author:

Grosberg Lauren E.1,Ganesan Karthik2,Goetz Georges A.1,Madugula Sasidhar S.1,Bhaskhar Nandita2,Fan Victoria1,Li Peter3,Hottowy Pawel4,Dabrowski Wladyslaw4,Sher Alexander5,Litke Alan M.5,Mitra Subhasish2,Chichilnisky E. J.1

Affiliation:

1. Department of Neurosurgery and Hansen Experimental Physics Laboratory, Stanford University, Stanford, California;

2. Departments of Electrical Engineering and Computer Science, Stanford University, Stanford, California;

3. Systems Neurobiology Laboratories, Salk Institute for Biological Studies, La Jolla, California;

4. Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Krakow, Poland; and

5. Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, Santa Cruz, California

Abstract

Epiretinal prostheses for treating blindness activate axon bundles, causing large, arc-shaped visual percepts that limit the quality of artificial vision. Improving the function of epiretinal prostheses therefore requires understanding and avoiding axon bundle activation. This study introduces a method to detect axon bundle activation on the basis of its electrical signature and uses the method to test whether epiretinal stimulation can directly elicit spikes in individual retinal ganglion cells without activating nearby axon bundles. Combined electrical stimulation and recording from isolated primate retina were performed using a custom multielectrode system (512 electrodes, 10-μm diameter, 60-μm pitch). Axon bundle signals were identified by their bidirectional propagation, speed, and increasing amplitude as a function of stimulation current. The threshold for bundle activation varied across electrodes and retinas, and was in the same range as the threshold for activating retinal ganglion cells near their somas. In the peripheral retina, 45% of electrodes that activated individual ganglion cells (17% of all electrodes) did so without activating bundles. This permitted selective activation of 21% of recorded ganglion cells (7% of expected ganglion cells) over the array. In one recording in the central retina, 75% of electrodes that activated individual ganglion cells (16% of all electrodes) did so without activating bundles. The ability to selectively activate a subset of retinal ganglion cells without axon bundles suggests a possible novel architecture for future epiretinal prostheses. NEW & NOTEWORTHY Large-scale multielectrode recording and stimulation were used to test how selectively retinal ganglion cells can be electrically activated without activating axon bundles. A novel method was developed to identify axon activation on the basis of its unique electrical signature and was used to find that a subset of ganglion cells can be activated at single-cell, single-spike resolution without producing bundle activity in peripheral and central retina. These findings have implications for the development of advanced retinal prostheses.

Funder

HHS | NIH | National Eye Institute (NEI)

NIH

National Science Foundation (NSF)

Narodowe Centrum Nauki (Polish National Science Centre)

Pew Charitable Trusts (PEW)

Publisher

American Physiological Society

Subject

Physiology,General Neuroscience

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