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Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons
Adaptation of visual responses enhances visual information processing mainly by preserving the full dynamic range of neuronal responses during changing light conditions and is found throughout the whole visual system. Although adaptation in the primate superior colliculus neurons has received much a...
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/PMC5997664/ https://www.ncbi.nlm.nih.gov/pubmed/29895940 http://dx.doi.org/10.1038/s41598-018-27331-2 |
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author | Bytautiene, Juntaute Baranauskas, Gytis |
author_facet | Bytautiene, Juntaute Baranauskas, Gytis |
author_sort | Bytautiene, Juntaute |
collection | PubMed |
description | Adaptation of visual responses enhances visual information processing mainly by preserving the full dynamic range of neuronal responses during changing light conditions and is found throughout the whole visual system. Although adaptation in the primate superior colliculus neurons has received much attention little is known about quantitative properties of such adaptation in rodents, an increasingly important model in vision research. By employing single unit recordings, we demonstrate that in the rat collicular neurons visual responses are shaped by at least two forms of adaptation. When visual stimuli were repeatedly presented in the same location, visual responses were reduced in the majority of single units. However, when the adaptor stimulus was outside a small diameter receptive field (RF), responses to stimulus onset but not offset were enhanced in the majority of units. Responses to stimulus offset were reduced less and recovered faster than responses to stimulus onset and the effect was limited to a fraction of RF area. Simulations showed that such adaptation acted as a powerful spatiotemporal filter and could explain several tuning properties of collicular neurons. These results demonstrate that in rodents the adaption of visual responses has a complex spatiotemporal structure and can profoundly shape visual information processing. |
format | Online Article Text |
id | pubmed-5997664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59976642018-06-21 Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons Bytautiene, Juntaute Baranauskas, Gytis Sci Rep Article Adaptation of visual responses enhances visual information processing mainly by preserving the full dynamic range of neuronal responses during changing light conditions and is found throughout the whole visual system. Although adaptation in the primate superior colliculus neurons has received much attention little is known about quantitative properties of such adaptation in rodents, an increasingly important model in vision research. By employing single unit recordings, we demonstrate that in the rat collicular neurons visual responses are shaped by at least two forms of adaptation. When visual stimuli were repeatedly presented in the same location, visual responses were reduced in the majority of single units. However, when the adaptor stimulus was outside a small diameter receptive field (RF), responses to stimulus onset but not offset were enhanced in the majority of units. Responses to stimulus offset were reduced less and recovered faster than responses to stimulus onset and the effect was limited to a fraction of RF area. Simulations showed that such adaptation acted as a powerful spatiotemporal filter and could explain several tuning properties of collicular neurons. These results demonstrate that in rodents the adaption of visual responses has a complex spatiotemporal structure and can profoundly shape visual information processing. Nature Publishing Group UK 2018-06-12 /pmc/articles/PMC5997664/ /pubmed/29895940 http://dx.doi.org/10.1038/s41598-018-27331-2 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 Bytautiene, Juntaute Baranauskas, Gytis Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title | Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title_full | Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title_fullStr | Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title_full_unstemmed | Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title_short | Experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
title_sort | experimentally derived model shows that adaptation acts as a powerful spatiotemporal filter of visual responses in the rat collicular neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997664/ https://www.ncbi.nlm.nih.gov/pubmed/29895940 http://dx.doi.org/10.1038/s41598-018-27331-2 |
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