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视觉行为障碍作为脆性X综合征小鼠模型中的一种异常感觉处理

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

作者信息

Felgerolle Chloé, Hébert Betty, Ardourel Maryvonne, Meyer-Dilhet Géraldine, Menuet Arnaud, Pinto-Morais Kimberley, Bizot Jean-Charles, Pichon Jacques, Briault Sylvain, Perche Olivier

机构信息

UMR7355, CNRS, Orléans, France.

Experimental and Molecular Immunology and Neurogenetics, University of Orléans, Orléans, France.

出版信息

Front Behav Neurosci. 2019 Oct 2;13:228. doi: 10.3389/fnbeh.2019.00228. eCollection 2019.

DOI:10.3389/fnbeh.2019.00228
PMID:31680892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6797836/
Abstract

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 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 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, 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.

摘要

脆性X综合征(FXS)是人类智力障碍(ID)最常见的遗传形式,与自闭症样行为相关,其特征是对感觉刺激,尤其是视觉刺激不敏感。在缺乏脆性智力迟缓蛋白(FMRP)的情况下,视觉通路的视网膜和脑结构都会受损,这表明视觉刺激的感知和整合发生了改变。然而,这些缺陷的行为后果仍然未知。在本研究中,我们使用雄性小鼠,通过关注表征视觉模式的三个特征:深度感知、对比度感知和运动感知,从行为学角度进一步明确视觉障碍。我们进行了特定测试(视动鼓、视觉悬崖)来评估这些视觉模式、它们从幼年到成年的发展变化,并评估它们在一项认知任务中的作用。我们发现小鼠的视觉技能出现改变,表现为透视感知受损、理解移动对比模式的能力下降以及对比度辨别缺陷。有趣的是,从青春期到成年后期,小鼠的这些表型随时间保持稳定。此外,我们报告颜色和形状对于完成一项涉及物体识别的认知测试具有重要意义。总之,这些结果强调了FXS条件下视觉行为改变的重要性,以及在进行涉及视觉辨别的行为任务(如认知评估)之前,在神经精神模型中评估视觉技能的相关性。

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2
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Front Mol Neurosci. 2018 Oct 2;11:353. doi: 10.3389/fnmol.2018.00353. eCollection 2018.
3
Impaired perceptual learning in a mouse model of Fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.
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PLoS Biol. 2025 Jul 1;23(7):e3003248. doi: 10.1371/journal.pbio.3003248. eCollection 2025 Jul.
4
Atypical retinal ganglion cell function in a mouse model of Fragile X syndrome.脆性X综合征小鼠模型中的非典型视网膜神经节细胞功能
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5
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6
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9
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