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Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models
The ability to preferentially stimulate different retinal pathways is an important area of research for improving visual prosthetics. Recent work has shown that different classes of retinal ganglion cells (RGCs) have distinct linear electrical input filters for low-amplitude white noise stimulation....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235533/ https://www.ncbi.nlm.nih.gov/pubmed/32477044 http://dx.doi.org/10.3389/fnins.2020.00378 |
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author | Sekhar, Sudarshan Ramesh, Poornima Bassetto, Giacomo Zrenner, Eberhart Macke, Jakob H. Rathbun, Daniel L. |
author_facet | Sekhar, Sudarshan Ramesh, Poornima Bassetto, Giacomo Zrenner, Eberhart Macke, Jakob H. Rathbun, Daniel L. |
author_sort | Sekhar, Sudarshan |
collection | PubMed |
description | The ability to preferentially stimulate different retinal pathways is an important area of research for improving visual prosthetics. Recent work has shown that different classes of retinal ganglion cells (RGCs) have distinct linear electrical input filters for low-amplitude white noise stimulation. The aim of this study is to provide a statistical framework for characterizing how RGCs respond to white-noise electrical stimulation. We used a nested family of Generalized Linear Models (GLMs) to partition neural responses into different components—progressively adding covariates to the GLM which captured non-stationarity in neural activity, a linear dependence on the stimulus, and any remaining non-linear interactions. We found that each of these components resulted in increased model performance, but that even the non-linear model left a substantial fraction of neural variability unexplained. The broad goal of this paper is to provide a much-needed theoretical framework to objectively quantify stimulus paradigms in terms of the types of neural responses that they elicit (linear vs. non-linear vs. stimulus-independent variability). In turn, this aids the prosthetic community in the search for optimal stimulus parameters that avoid indiscriminate retinal activation and adaptation caused by excessively large stimulus pulses, and avoid low fidelity responses (low signal-to-noise ratio) caused by excessively weak stimulus pulses. |
format | Online Article Text |
id | pubmed-7235533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72355332020-05-29 Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models Sekhar, Sudarshan Ramesh, Poornima Bassetto, Giacomo Zrenner, Eberhart Macke, Jakob H. Rathbun, Daniel L. Front Neurosci Neuroscience The ability to preferentially stimulate different retinal pathways is an important area of research for improving visual prosthetics. Recent work has shown that different classes of retinal ganglion cells (RGCs) have distinct linear electrical input filters for low-amplitude white noise stimulation. The aim of this study is to provide a statistical framework for characterizing how RGCs respond to white-noise electrical stimulation. We used a nested family of Generalized Linear Models (GLMs) to partition neural responses into different components—progressively adding covariates to the GLM which captured non-stationarity in neural activity, a linear dependence on the stimulus, and any remaining non-linear interactions. We found that each of these components resulted in increased model performance, but that even the non-linear model left a substantial fraction of neural variability unexplained. The broad goal of this paper is to provide a much-needed theoretical framework to objectively quantify stimulus paradigms in terms of the types of neural responses that they elicit (linear vs. non-linear vs. stimulus-independent variability). In turn, this aids the prosthetic community in the search for optimal stimulus parameters that avoid indiscriminate retinal activation and adaptation caused by excessively large stimulus pulses, and avoid low fidelity responses (low signal-to-noise ratio) caused by excessively weak stimulus pulses. Frontiers Media S.A. 2020-05-12 /pmc/articles/PMC7235533/ /pubmed/32477044 http://dx.doi.org/10.3389/fnins.2020.00378 Text en Copyright © 2020 Sekhar, Ramesh, Bassetto, Zrenner, Macke and Rathbun. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Sekhar, Sudarshan Ramesh, Poornima Bassetto, Giacomo Zrenner, Eberhart Macke, Jakob H. Rathbun, Daniel L. Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title | Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title_full | Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title_fullStr | Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title_full_unstemmed | Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title_short | Characterizing Retinal Ganglion Cell Responses to Electrical Stimulation Using Generalized Linear Models |
title_sort | characterizing retinal ganglion cell responses to electrical stimulation using generalized linear models |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235533/ https://www.ncbi.nlm.nih.gov/pubmed/32477044 http://dx.doi.org/10.3389/fnins.2020.00378 |
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