Vit Jean-Philippe, Fuchs Dieu-Trang, Angel Ariel, Levy Aharon, Lamensdorf Itschak, Black Keith L, Koronyo Yosef, Koronyo-Hamaoui Maya
Department of Neurosurgery, Maxine Dunitz Neurosurgical Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.
Pharmaseed Ltd., Ness Ziona 74047, Israel.
Bio Protoc. 2021 Nov 20;11(22):e4234. doi: 10.21769/BioProtoc.4234.
Visual impairments, notably loss of contrast sensitivity and color vision, were documented in Alzheimer's disease (AD) patients yet are critically understudied. This protocol describes a novel visual-stimuli four-arm maze (ViS4M; also called visual x-maze), which is a versatile x-shaped maze equipped with spectrum- and intensity-controlled light-emitting diode (LED) sources and dynamic grayscale objects. The ViS4M is designed to allow the assessment of color and contrast vision along with locomotor and cognitive functions in mice. In the color testing mode, the spectral distributions of the LED lights create four homogenous spaces that differ in chromaticity and luminance, corresponding to the mouse visual system. In the contrast sensitivity test, the four grayscale objects are placed in the middle of each arm, contrasting against the black walls and the white floors of the maze. Upon entering the maze, healthy wild-type (WT) mice tend to spontaneously alternate between arms, even under equiluminant conditions of illumination, suggesting that cognitively and visually intact mice use both color and brightness as cues to navigate the maze. Evaluation of the double-transgenic APP/PS1 mouse model of AD (AD mice) reveals substantial deficits to alternate in both color and contrast modes at an early age, when hippocampal-based memory and learning is still intact. Profiling of timespan, entries, and transition patterns between the different arms uncovers variable aging and AD-associated impairments in color discrimination and contrast sensitivity. The analysis of arm sequences of alternation reveals different pathways of exploration in young WT, old WT, and AD mice, which can be used as color and contrast imprints of functionally intact versus impaired mice. Overall, we describe the utility of a novel visual x-maze test to identify behavioral changes in mice related to cognition, as well as color and contrast vision, with high precision and reproducibility. Graphic abstract: Exploratory behavior of AD mice versus age- and sex-matched WT mice is tracked (top left: trajectory from a 5-min video file) in a novel visual-stimuli four-arm maze (ViS4M; also named visual x-maze) equipped with spectrum- and intensity-controlled LED sources or grayscale objects. Consecutive arm entries reveal that APP/PS1 (AD) mice alternate less between arms, as opposed to WT mice. Sequence analysis, according to the three alternation pathways (depicted by white, yellow, and brown arrows) under different conditions of illumination, uncovers specific deficits linked to color vision in AD mice, evidenced by a color imprint chart.
视觉障碍,尤其是对比敏感度和色觉丧失,在阿尔茨海默病(AD)患者中已有记录,但仍未得到充分研究。本方案描述了一种新型视觉刺激四臂迷宫(ViS4M;也称为视觉十字迷宫),它是一种多功能的十字形迷宫,配备了光谱和强度可控的发光二极管(LED)光源以及动态灰度物体。ViS4M旨在用于评估小鼠的色觉和对比视觉以及运动和认知功能。在颜色测试模式下,LED灯的光谱分布创建了四个在色度和亮度上不同的均匀空间,与小鼠视觉系统相对应。在对比敏感度测试中,四个灰度物体放置在每个臂的中间,与迷宫的黑色墙壁和白色地板形成对比。进入迷宫后,健康的野生型(WT)小鼠即使在等亮度照明条件下也倾向于在各臂之间自发交替,这表明认知和视觉功能正常的小鼠利用颜色和亮度作为线索来导航迷宫。对AD的双转基因APP/PS1小鼠模型(AD小鼠)的评估显示,在基于海马的记忆和学习功能仍然完好的早期,它们在颜色和对比模式下交替的能力存在显著缺陷。对不同臂之间的时间跨度、进入次数和转换模式进行分析,发现了与衰老和AD相关的颜色辨别和对比敏感度损伤的差异。对交替臂序列的分析揭示了年轻WT小鼠、老年WT小鼠和AD小鼠不同的探索路径,这些路径可作为功能正常与受损小鼠的颜色和对比印记。总体而言,我们描述了一种新型视觉十字迷宫测试的效用,它能够高精度且可重复地识别小鼠与认知以及颜色和对比视觉相关的行为变化。图形摘要:在配备光谱和强度可控LED光源或灰度物体的新型视觉刺激四臂迷宫(ViS4M;也称为视觉十字迷宫)中,追踪AD小鼠与年龄和性别匹配的WT小鼠的探索行为(左上角:来自5分钟视频文件的轨迹)。连续的臂进入情况显示,与WT小鼠相比,APP/PS1(AD)小鼠在各臂之间的交替较少。根据不同照明条件下的三种交替路径(由白色、黄色和棕色箭头表示)进行序列分析,发现AD小鼠存在与色觉相关的特定缺陷,这由颜色印记图表证明。