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Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice
Recent translational studies using mice have contributed toward elucidating the neural, genetic, and molecular basis of social communication deficits. Nevertheless, many components of visual processes underlying mice sociality remain unresolved, including perception of bodily-movement. Here, we aime...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232871/ https://www.ncbi.nlm.nih.gov/pubmed/30459572 http://dx.doi.org/10.3389/fnbeh.2018.00263 |
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author | Atsumi, Takeshi Ide, Masakazu Wada, Makoto |
author_facet | Atsumi, Takeshi Ide, Masakazu Wada, Makoto |
author_sort | Atsumi, Takeshi |
collection | PubMed |
description | Recent translational studies using mice have contributed toward elucidating the neural, genetic, and molecular basis of social communication deficits. Nevertheless, many components of visual processes underlying mice sociality remain unresolved, including perception of bodily-movement. Here, we aimed to reveal the visual sensitivity of mice to information on bodily motion using biological motion displays depicted by simple geometric dots. We introduced biological motions extracted from walking mice vs. corresponding meaningless scrambled motions, in which the spatial configurations of each path of dots were shuffled. The apparatus was a three-chambered box with an opening between the chambers, and each side chamber had a monitor. We measured the exploration time of mice within the apparatus during the test, with two types of displays being presented. Mice spent more time in the chamber with the scrambled motion displays, indicating that animals spontaneously discriminated stimuli, with the scrambled motion being relatively novel. Furthermore, mice might have detected socially familiar cues from the biological motion displays. Subsequent testing revealed that additional mice showed no bias to the static versions of the stimuli used in the Movie test. Thus, we confirmed that mice modulated their behavior by focusing on the motion information of the stimuli, rather than the spatial configurations of each dot. Our findings provide a new perspective on how visual processing contributes to underlying social behavior in mice, potentially facilitating future translational studies of social deficits with respect to genetic and neural bases. |
format | Online Article Text |
id | pubmed-6232871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62328712018-11-20 Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice Atsumi, Takeshi Ide, Masakazu Wada, Makoto Front Behav Neurosci Neuroscience Recent translational studies using mice have contributed toward elucidating the neural, genetic, and molecular basis of social communication deficits. Nevertheless, many components of visual processes underlying mice sociality remain unresolved, including perception of bodily-movement. Here, we aimed to reveal the visual sensitivity of mice to information on bodily motion using biological motion displays depicted by simple geometric dots. We introduced biological motions extracted from walking mice vs. corresponding meaningless scrambled motions, in which the spatial configurations of each path of dots were shuffled. The apparatus was a three-chambered box with an opening between the chambers, and each side chamber had a monitor. We measured the exploration time of mice within the apparatus during the test, with two types of displays being presented. Mice spent more time in the chamber with the scrambled motion displays, indicating that animals spontaneously discriminated stimuli, with the scrambled motion being relatively novel. Furthermore, mice might have detected socially familiar cues from the biological motion displays. Subsequent testing revealed that additional mice showed no bias to the static versions of the stimuli used in the Movie test. Thus, we confirmed that mice modulated their behavior by focusing on the motion information of the stimuli, rather than the spatial configurations of each dot. Our findings provide a new perspective on how visual processing contributes to underlying social behavior in mice, potentially facilitating future translational studies of social deficits with respect to genetic and neural bases. Frontiers Media S.A. 2018-11-06 /pmc/articles/PMC6232871/ /pubmed/30459572 http://dx.doi.org/10.3389/fnbeh.2018.00263 Text en Copyright © 2018 Atsumi, Ide and Wada. 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 Atsumi, Takeshi Ide, Masakazu Wada, Makoto Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title | Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title_full | Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title_fullStr | Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title_full_unstemmed | Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title_short | Spontaneous Discriminative Response to the Biological Motion Displays Involving a Walking Conspecific in Mice |
title_sort | spontaneous discriminative response to the biological motion displays involving a walking conspecific in mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232871/ https://www.ncbi.nlm.nih.gov/pubmed/30459572 http://dx.doi.org/10.3389/fnbeh.2018.00263 |
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