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Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum

Evolutionary development of vision has provided us with the capacity to detect moving objects. Concordant shifts of visual features suggest movements of the observer, whereas discordant changes are more likely to be indicating independently moving objects, such as predators or prey. Such distinction...

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Detalles Bibliográficos
Autores principales: Nagy, Anett J., Takeuchi, Yuichi, Berényi, Antal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034886/
https://www.ncbi.nlm.nih.gov/pubmed/29939998
http://dx.doi.org/10.1371/journal.pbio.2004712
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author Nagy, Anett J.
Takeuchi, Yuichi
Berényi, Antal
author_facet Nagy, Anett J.
Takeuchi, Yuichi
Berényi, Antal
author_sort Nagy, Anett J.
collection PubMed
description Evolutionary development of vision has provided us with the capacity to detect moving objects. Concordant shifts of visual features suggest movements of the observer, whereas discordant changes are more likely to be indicating independently moving objects, such as predators or prey. Such distinction helps us to focus attention, adapt our behavior, and adjust our motor patterns to meet behavioral challenges. However, the neural basis of distinguishing self-induced and self-independent visual motions is not clarified in unrestrained animals yet. In this study, we investigated the presence and origin of motion-related visual information in the striatum of rats, a hub of action selection and procedural memory. We found that while almost half of the neurons in the dorsomedial striatum are sensitive to visual motion congruent with locomotion (and that many of them also code for spatial location), only a small subset of them are composed of fast-firing interneurons that could also perceive self-independent visual stimuli. These latter cells receive their visual input at least partially from the secondary visual cortex (V2). This differential visual sensitivity may be an important support in adjusting behavior to salient environmental events. It emphasizes the importance of investigating visual motion perception in unrestrained animals.
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spelling pubmed-60348862018-07-19 Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum Nagy, Anett J. Takeuchi, Yuichi Berényi, Antal PLoS Biol Research Article Evolutionary development of vision has provided us with the capacity to detect moving objects. Concordant shifts of visual features suggest movements of the observer, whereas discordant changes are more likely to be indicating independently moving objects, such as predators or prey. Such distinction helps us to focus attention, adapt our behavior, and adjust our motor patterns to meet behavioral challenges. However, the neural basis of distinguishing self-induced and self-independent visual motions is not clarified in unrestrained animals yet. In this study, we investigated the presence and origin of motion-related visual information in the striatum of rats, a hub of action selection and procedural memory. We found that while almost half of the neurons in the dorsomedial striatum are sensitive to visual motion congruent with locomotion (and that many of them also code for spatial location), only a small subset of them are composed of fast-firing interneurons that could also perceive self-independent visual stimuli. These latter cells receive their visual input at least partially from the secondary visual cortex (V2). This differential visual sensitivity may be an important support in adjusting behavior to salient environmental events. It emphasizes the importance of investigating visual motion perception in unrestrained animals. Public Library of Science 2018-06-25 /pmc/articles/PMC6034886/ /pubmed/29939998 http://dx.doi.org/10.1371/journal.pbio.2004712 Text en © 2018 Nagy et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nagy, Anett J.
Takeuchi, Yuichi
Berényi, Antal
Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title_full Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title_fullStr Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title_full_unstemmed Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title_short Coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
title_sort coding of self-motion-induced and self-independent visual motion in the rat dorsomedial striatum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034886/
https://www.ncbi.nlm.nih.gov/pubmed/29939998
http://dx.doi.org/10.1371/journal.pbio.2004712
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