Cargando…

Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome

Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence of Fragile Mental Retardation Protein (FMRP), both retinal and cerebral st...

Descripción completa

Detalles Bibliográficos
Autores principales: Felgerolle, Chloé, Hébert, Betty, Ardourel, Maryvonne, Meyer-Dilhet, Géraldine, Menuet, Arnaud, Pinto-Morais, Kimberley, Bizot, Jean-Charles, Pichon, Jacques, Briault, Sylvain, Perche, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797836/
https://www.ncbi.nlm.nih.gov/pubmed/31680892
http://dx.doi.org/10.3389/fnbeh.2019.00228
_version_ 1783459922875252736
author Felgerolle, Chloé
Hébert, Betty
Ardourel, Maryvonne
Meyer-Dilhet, Géraldine
Menuet, Arnaud
Pinto-Morais, Kimberley
Bizot, Jean-Charles
Pichon, Jacques
Briault, Sylvain
Perche, Olivier
author_facet Felgerolle, Chloé
Hébert, Betty
Ardourel, Maryvonne
Meyer-Dilhet, Géraldine
Menuet, Arnaud
Pinto-Morais, Kimberley
Bizot, Jean-Charles
Pichon, Jacques
Briault, Sylvain
Perche, Olivier
author_sort Felgerolle, Chloé
collection PubMed
description Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence of Fragile Mental Retardation Protein (FMRP), both retinal and cerebral structures of the visual pathway are impaired, suggesting that perception and integration of visual stimuli are altered. However, behavioral consequences of these defects remain unknown. In this study, we used male Fmr1(−/y) mice to further define visual disturbances from a behavioral perspective by focusing on three traits characterizing visual modality: perception of depth, contrasts and movements. We performed specific tests (Optomotor Drum, Visual Cliff) to evaluate these visual modalities, their evolution from youth to adulthood, and to assess their involvement in a cognitive task. We show that Fmr1(−/y) mice exhibit alteration in their visual skills, displaying impaired perspective perception, a drop in their ability to understand a moving contrasted pattern, and a defect in contrasts discrimination. Interestingly, Fmr1(−/y) phenotypes remain stable over time from adolescence to late adulthood. Besides, we report that color and shape are meaningful for the achievement of a cognitive test involving object recognition. Altogether, these results underline the significance of visual behavior alterations in FXS conditions and relevance of assessing visual skills in neuropsychiatric models before performing behavioral tasks, such as cognitive assessments, that involve visual discrimination.
format Online
Article
Text
id pubmed-6797836
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-67978362019-11-01 Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome Felgerolle, Chloé Hébert, Betty Ardourel, Maryvonne Meyer-Dilhet, Géraldine Menuet, Arnaud Pinto-Morais, Kimberley Bizot, Jean-Charles Pichon, Jacques Briault, Sylvain Perche, Olivier Front Behav Neurosci Behavioral Neuroscience Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence of Fragile Mental Retardation Protein (FMRP), both retinal and cerebral structures of the visual pathway are impaired, suggesting that perception and integration of visual stimuli are altered. However, behavioral consequences of these defects remain unknown. In this study, we used male Fmr1(−/y) mice to further define visual disturbances from a behavioral perspective by focusing on three traits characterizing visual modality: perception of depth, contrasts and movements. We performed specific tests (Optomotor Drum, Visual Cliff) to evaluate these visual modalities, their evolution from youth to adulthood, and to assess their involvement in a cognitive task. We show that Fmr1(−/y) mice exhibit alteration in their visual skills, displaying impaired perspective perception, a drop in their ability to understand a moving contrasted pattern, and a defect in contrasts discrimination. Interestingly, Fmr1(−/y) phenotypes remain stable over time from adolescence to late adulthood. Besides, we report that color and shape are meaningful for the achievement of a cognitive test involving object recognition. Altogether, these results underline the significance of visual behavior alterations in FXS conditions and relevance of assessing visual skills in neuropsychiatric models before performing behavioral tasks, such as cognitive assessments, that involve visual discrimination. Frontiers Media S.A. 2019-10-02 /pmc/articles/PMC6797836/ /pubmed/31680892 http://dx.doi.org/10.3389/fnbeh.2019.00228 Text en Copyright © 2019 Felgerolle, Hébert, Ardourel, Meyer-Dilhet, Menuet, Pinto-Morais, Bizot, Pichon, Briault and Perche. 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 Behavioral Neuroscience
Felgerolle, Chloé
Hébert, Betty
Ardourel, Maryvonne
Meyer-Dilhet, Géraldine
Menuet, Arnaud
Pinto-Morais, Kimberley
Bizot, Jean-Charles
Pichon, Jacques
Briault, Sylvain
Perche, Olivier
Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title_full Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title_fullStr Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title_full_unstemmed Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title_short Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome
title_sort visual behavior impairments as an aberrant sensory processing in the mouse model of fragile x syndrome
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797836/
https://www.ncbi.nlm.nih.gov/pubmed/31680892
http://dx.doi.org/10.3389/fnbeh.2019.00228
work_keys_str_mv AT felgerollechloe visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT hebertbetty visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT ardourelmaryvonne visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT meyerdilhetgeraldine visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT menuetarnaud visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT pintomoraiskimberley visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT bizotjeancharles visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT pichonjacques visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT briaultsylvain visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome
AT percheolivier visualbehaviorimpairmentsasanaberrantsensoryprocessinginthemousemodeloffragilexsyndrome