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Atypical visual processing in a mouse model of autism

Human social cognition relies heavily on the processing of various visual cues, such as eye contact and facial expressions. Atypical visual perception and integration have been recognized as key phenotypes in individuals diagnosed with autism spectrum disorder (ASD), and may potentially contribute t...

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Autores principales: Cheng, Ning, Pagtalunan, Eden, Abushaibah, Abdulrahman, Naidu, Jessica, Stell, William K., Rho, Jong M., Sauvé, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381655/
https://www.ncbi.nlm.nih.gov/pubmed/32709898
http://dx.doi.org/10.1038/s41598-020-68589-9
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author Cheng, Ning
Pagtalunan, Eden
Abushaibah, Abdulrahman
Naidu, Jessica
Stell, William K.
Rho, Jong M.
Sauvé, Yves
author_facet Cheng, Ning
Pagtalunan, Eden
Abushaibah, Abdulrahman
Naidu, Jessica
Stell, William K.
Rho, Jong M.
Sauvé, Yves
author_sort Cheng, Ning
collection PubMed
description Human social cognition relies heavily on the processing of various visual cues, such as eye contact and facial expressions. Atypical visual perception and integration have been recognized as key phenotypes in individuals diagnosed with autism spectrum disorder (ASD), and may potentially contribute to impediments in normal social development, a hallmark of ASD. Meanwhile, increasing studies on visual function in ASD have pointed to detail-oriented perception, which has been hypothesized to result from heightened response to information of high spatial frequency. However, mixed results of human studies have led to much debate, and investigations using animal models have been limited. Here, using BTBR mice as a model of idiopathic ASD, we assessed retinal stimulus processing by full-field electroretinogram and found impaired photoreceptor function and retina-based alterations mostly in the cone pathway. Using the optokinetic reflex to evaluate visual function, we observed robustly enhanced visual response to finer spatial details and more subtle contrasts at only higher spatial frequencies in the BTBR mice, under both photopic and scotopic conditions. These behavioral results, which are similar to findings in a subset of ASD patients, indicate a bias toward processing information of high spatial frequencies. Together, these findings also suggest that, while enhancement of visual behaviors under both photopic and scotopic conditions might be due to alterations in visual processing common to both rod and cone pathways, these mechanisms are probably downstream of photoreceptor function.
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spelling pubmed-73816552020-07-28 Atypical visual processing in a mouse model of autism Cheng, Ning Pagtalunan, Eden Abushaibah, Abdulrahman Naidu, Jessica Stell, William K. Rho, Jong M. Sauvé, Yves Sci Rep Article Human social cognition relies heavily on the processing of various visual cues, such as eye contact and facial expressions. Atypical visual perception and integration have been recognized as key phenotypes in individuals diagnosed with autism spectrum disorder (ASD), and may potentially contribute to impediments in normal social development, a hallmark of ASD. Meanwhile, increasing studies on visual function in ASD have pointed to detail-oriented perception, which has been hypothesized to result from heightened response to information of high spatial frequency. However, mixed results of human studies have led to much debate, and investigations using animal models have been limited. Here, using BTBR mice as a model of idiopathic ASD, we assessed retinal stimulus processing by full-field electroretinogram and found impaired photoreceptor function and retina-based alterations mostly in the cone pathway. Using the optokinetic reflex to evaluate visual function, we observed robustly enhanced visual response to finer spatial details and more subtle contrasts at only higher spatial frequencies in the BTBR mice, under both photopic and scotopic conditions. These behavioral results, which are similar to findings in a subset of ASD patients, indicate a bias toward processing information of high spatial frequencies. Together, these findings also suggest that, while enhancement of visual behaviors under both photopic and scotopic conditions might be due to alterations in visual processing common to both rod and cone pathways, these mechanisms are probably downstream of photoreceptor function. Nature Publishing Group UK 2020-07-24 /pmc/articles/PMC7381655/ /pubmed/32709898 http://dx.doi.org/10.1038/s41598-020-68589-9 Text en © The Author(s) 2020 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
Cheng, Ning
Pagtalunan, Eden
Abushaibah, Abdulrahman
Naidu, Jessica
Stell, William K.
Rho, Jong M.
Sauvé, Yves
Atypical visual processing in a mouse model of autism
title Atypical visual processing in a mouse model of autism
title_full Atypical visual processing in a mouse model of autism
title_fullStr Atypical visual processing in a mouse model of autism
title_full_unstemmed Atypical visual processing in a mouse model of autism
title_short Atypical visual processing in a mouse model of autism
title_sort atypical visual processing in a mouse model of autism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381655/
https://www.ncbi.nlm.nih.gov/pubmed/32709898
http://dx.doi.org/10.1038/s41598-020-68589-9
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