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Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss

The Royal College of Surgeons (RCS) rat gradually loses vision due to retinal degeneration. Previous physiological studies have depicted the progressive loss of optical responses in the visual pathway, including the primary visual cortex (V1), over the course of retinal degeneration in the RCS rat....

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Autores principales: Miyamoto, Soshi, Suematsu, Naofumi, Umehira, Yuichi, Hayashida, Yuki, Yagi, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658441/
https://www.ncbi.nlm.nih.gov/pubmed/29075008
http://dx.doi.org/10.1038/s41598-017-14303-1
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author Miyamoto, Soshi
Suematsu, Naofumi
Umehira, Yuichi
Hayashida, Yuki
Yagi, Tetsuya
author_facet Miyamoto, Soshi
Suematsu, Naofumi
Umehira, Yuichi
Hayashida, Yuki
Yagi, Tetsuya
author_sort Miyamoto, Soshi
collection PubMed
description The Royal College of Surgeons (RCS) rat gradually loses vision due to retinal degeneration. Previous physiological studies have depicted the progressive loss of optical responses in the visual pathway, including the primary visual cortex (V1), over the course of retinal degeneration in the RCS rat. However, little is known about how the excitability of the V1 circuit changes during over the course of the gradual loss of visual signal input from the retina. We elucidated the properties of responses to electrical stimulations directly applied to V1 at different stages of vision input loss in the RCS rat in reference to those of the Long-Evans (LE) rat, using in vivo voltage-sensitive dye imaging. The V1 neuronal network of the RCS rat exhibited an excitatory response comparable to the LE rat. The excitatory response was maintained even long after total loss of the visual signal input from the retina. However, the response time-course suggested that the suppressive response was somewhat debilitated in the RCS rat. This is the first experiment demonstrating the long-term effect of retinal degeneration on cortical activities. Our findings provide the physiological fundamentals to enhance the preclinical research of cortical prostheses with the use of the RCS rat.
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spelling pubmed-56584412017-10-31 Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss Miyamoto, Soshi Suematsu, Naofumi Umehira, Yuichi Hayashida, Yuki Yagi, Tetsuya Sci Rep Article The Royal College of Surgeons (RCS) rat gradually loses vision due to retinal degeneration. Previous physiological studies have depicted the progressive loss of optical responses in the visual pathway, including the primary visual cortex (V1), over the course of retinal degeneration in the RCS rat. However, little is known about how the excitability of the V1 circuit changes during over the course of the gradual loss of visual signal input from the retina. We elucidated the properties of responses to electrical stimulations directly applied to V1 at different stages of vision input loss in the RCS rat in reference to those of the Long-Evans (LE) rat, using in vivo voltage-sensitive dye imaging. The V1 neuronal network of the RCS rat exhibited an excitatory response comparable to the LE rat. The excitatory response was maintained even long after total loss of the visual signal input from the retina. However, the response time-course suggested that the suppressive response was somewhat debilitated in the RCS rat. This is the first experiment demonstrating the long-term effect of retinal degeneration on cortical activities. Our findings provide the physiological fundamentals to enhance the preclinical research of cortical prostheses with the use of the RCS rat. Nature Publishing Group UK 2017-10-26 /pmc/articles/PMC5658441/ /pubmed/29075008 http://dx.doi.org/10.1038/s41598-017-14303-1 Text en © The Author(s) 2017 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
Miyamoto, Soshi
Suematsu, Naofumi
Umehira, Yuichi
Hayashida, Yuki
Yagi, Tetsuya
Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title_full Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title_fullStr Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title_full_unstemmed Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title_short Age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
title_sort age-related changes in the spatiotemporal responses to electrical stimulation in the visual cortex of rats with progressive vision loss
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658441/
https://www.ncbi.nlm.nih.gov/pubmed/29075008
http://dx.doi.org/10.1038/s41598-017-14303-1
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