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Focal Electrical Stimulation of Human Retinal Ganglion Cells

Sasi Madugula, View ORCID ProfileAlex R. Gogliettino, Moosa Zaidi, Gorish Aggarwal, View ORCID ProfileAlexandra Kling, View ORCID ProfileNishal P. Shah, View ORCID ProfileRamandeep Vilkhu, Maddy Hays, Huy Nguyen, View ORCID ProfileVictoria Fan, View ORCID ProfileEric G. Wu, View ORCID ProfilePawel Hottowy, Alexander Sher, Alan M. Litke, Ruwan A. Silva, View ORCID ProfileE.J. Chichilnisky
doi: https://doi.org/10.1101/2020.08.23.263608
Sasi Madugula
3Neurosciences PhD Program, Stanford University, Stanford, CA, USA
4School of Medicine, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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Alex R. Gogliettino
3Neurosciences PhD Program, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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  • ORCID record for Alex R. Gogliettino
Moosa Zaidi
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
4School of Medicine, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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Gorish Aggarwal
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
2Department of Electrical Engineering, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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Alexandra Kling
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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  • ORCID record for Alexandra Kling
Nishal P. Shah
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
2Department of Electrical Engineering, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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Ramandeep Vilkhu
2Department of Electrical Engineering, Stanford University, Stanford, CA, USA
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  • ORCID record for Ramandeep Vilkhu
Maddy Hays
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
8Department of Bioengineering, Stanford University, Stanford, CA, USA
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Huy Nguyen
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
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Victoria Fan
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
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  • ORCID record for Victoria Fan
Eric G. Wu
2Department of Electrical Engineering, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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Pawel Hottowy
9Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Krakow, Poland
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Alexander Sher
5Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, CA, USA
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Alan M. Litke
5Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, CA, USA
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Ruwan A. Silva
6Department of Ophthalmology, Stanford University, Stanford, CA, USA
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E.J. Chichilnisky
1Department of Neurosurgery, Stanford University, Stanford, CA, USA
6Department of Ophthalmology, Stanford University, Stanford, CA, USA
7Hansen Experimental Physics Laboratory, Stanford University, Stanford, CA, USA
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  • For correspondence: ej@stanford.edu
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ABSTRACT

Electrical stimulation of retinal ganglion cells (RGCs), which transmit visual information to the brain, is used in retinal implants to treat blindness caused by photoreceptor degeneration. However, the performance of existing clinical implants is limited by indiscriminate stimulation of many cells and cell types. Recent work in isolated macaque retina has shown the ability to precisely evoke spikes in the major RGC types by direct electrical stimulation at safe current levels, with single-cell, single-spike resolution and avoidance of axon bundle activation in many cases. However, these findings have not been verified in the human retina. Here, electrical activation of the major human RGC types was examined using large-scale, multi-electrode recording and stimulation and compared to results from several macaque retinas obtained using the same methods. Electrical stimulation of the major human RGC types closely paralleled results in macaque, with similar somatic and axonal stimulation thresholds, cellular and cell type selectivity of stimulation, avoidance of axon bundle stimulation by calibration, targeting of different cell types based on their distinct electrical signatures, and potential efficacy of real-time stimulus optimization for artificial vision. The results indicate that the macaque retina provides a quantitatively accurate picture of how focal electrical stimulation can be used in future high-resolution implants.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted August 24, 2020.
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Focal Electrical Stimulation of Human Retinal Ganglion Cells
Sasi Madugula, Alex R. Gogliettino, Moosa Zaidi, Gorish Aggarwal, Alexandra Kling, Nishal P. Shah, Ramandeep Vilkhu, Maddy Hays, Huy Nguyen, Victoria Fan, Eric G. Wu, Pawel Hottowy, Alexander Sher, Alan M. Litke, Ruwan A. Silva, E.J. Chichilnisky
bioRxiv 2020.08.23.263608; doi: https://doi.org/10.1101/2020.08.23.263608
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Focal Electrical Stimulation of Human Retinal Ganglion Cells
Sasi Madugula, Alex R. Gogliettino, Moosa Zaidi, Gorish Aggarwal, Alexandra Kling, Nishal P. Shah, Ramandeep Vilkhu, Maddy Hays, Huy Nguyen, Victoria Fan, Eric G. Wu, Pawel Hottowy, Alexander Sher, Alan M. Litke, Ruwan A. Silva, E.J. Chichilnisky
bioRxiv 2020.08.23.263608; doi: https://doi.org/10.1101/2020.08.23.263608

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