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Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis
Subretinal prostheses are designed to restore sight in patients blinded by retinal degeneration using electrical stimulation of the inner retinal neurons. To relate retinal output to perception, we studied behavioral thresholds in blind rats with photovoltaic subretinal prostheses stimulated by full...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816604/ https://www.ncbi.nlm.nih.gov/pubmed/29453455 http://dx.doi.org/10.1038/s41598-018-21447-1 |
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author | Ho, Elton Lorach, Henri Goetz, Georges Laszlo, Florian Lei, Xin Kamins, Theodore Mariani, Jean-Charles Sher, Alexander Palanker, Daniel |
author_facet | Ho, Elton Lorach, Henri Goetz, Georges Laszlo, Florian Lei, Xin Kamins, Theodore Mariani, Jean-Charles Sher, Alexander Palanker, Daniel |
author_sort | Ho, Elton |
collection | PubMed |
description | Subretinal prostheses are designed to restore sight in patients blinded by retinal degeneration using electrical stimulation of the inner retinal neurons. To relate retinal output to perception, we studied behavioral thresholds in blind rats with photovoltaic subretinal prostheses stimulated by full-field pulsed illumination at 20 Hz, and measured retinal ganglion cell (RGC) responses to similar stimuli ex-vivo. Behaviorally, rats exhibited startling response to changes in brightness, with an average contrast threshold of 12%, which could not be explained by changes in the average RGC spiking rate. However, RGCs exhibited millisecond-scale variations in spike timing, even when the average rate did not change significantly. At 12% temporal contrast, changes in firing patterns of prosthetic response were as significant as with 2.3% contrast steps in visible light stimulation of healthy retinas. This suggests that millisecond-scale changes in spiking patterns define perceptual thresholds of prosthetic vision. Response to the last pulse in the stimulation burst lasted longer than the steady-state response during the burst. This may be interpreted as an excitatory OFF response to prosthetic stimulation, and can explain behavioral response to decrease in illumination. Contrast enhancement of images prior to delivery to subretinal prosthesis can partially compensate for reduced contrast sensitivity of prosthetic vision. |
format | Online Article Text |
id | pubmed-5816604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58166042018-02-21 Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis Ho, Elton Lorach, Henri Goetz, Georges Laszlo, Florian Lei, Xin Kamins, Theodore Mariani, Jean-Charles Sher, Alexander Palanker, Daniel Sci Rep Article Subretinal prostheses are designed to restore sight in patients blinded by retinal degeneration using electrical stimulation of the inner retinal neurons. To relate retinal output to perception, we studied behavioral thresholds in blind rats with photovoltaic subretinal prostheses stimulated by full-field pulsed illumination at 20 Hz, and measured retinal ganglion cell (RGC) responses to similar stimuli ex-vivo. Behaviorally, rats exhibited startling response to changes in brightness, with an average contrast threshold of 12%, which could not be explained by changes in the average RGC spiking rate. However, RGCs exhibited millisecond-scale variations in spike timing, even when the average rate did not change significantly. At 12% temporal contrast, changes in firing patterns of prosthetic response were as significant as with 2.3% contrast steps in visible light stimulation of healthy retinas. This suggests that millisecond-scale changes in spiking patterns define perceptual thresholds of prosthetic vision. Response to the last pulse in the stimulation burst lasted longer than the steady-state response during the burst. This may be interpreted as an excitatory OFF response to prosthetic stimulation, and can explain behavioral response to decrease in illumination. Contrast enhancement of images prior to delivery to subretinal prosthesis can partially compensate for reduced contrast sensitivity of prosthetic vision. Nature Publishing Group UK 2018-02-16 /pmc/articles/PMC5816604/ /pubmed/29453455 http://dx.doi.org/10.1038/s41598-018-21447-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ho, Elton Lorach, Henri Goetz, Georges Laszlo, Florian Lei, Xin Kamins, Theodore Mariani, Jean-Charles Sher, Alexander Palanker, Daniel Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title | Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title_full | Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title_fullStr | Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title_full_unstemmed | Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title_short | Temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
title_sort | temporal structure in spiking patterns of ganglion cells defines perceptual thresholds in rodents with subretinal prosthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816604/ https://www.ncbi.nlm.nih.gov/pubmed/29453455 http://dx.doi.org/10.1038/s41598-018-21447-1 |
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