Visuo-spatial learning and memory impairments in the 5xFAD mouse model of Alzheimer's disease: Effects of age, sex, albinism, and motor impairments

IF 2.4 4区 心理学 Q2 BEHAVIORAL SCIENCES
Timothy P. O'Leary, Richard E. Brown
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引用次数: 18

Abstract

The 5xFAD mouse model of Alzheimer's disease (AD) rapidly develops AD-related neuro-behavioral pathology. Learning and memory impairments in 5xFAD mice, however, are not always replicated and the size of impairments varies considerably across studies. To examine possible sources of this variability, we analyzed the effects of age, sex, albinism due to background genes (Tyrc, Oca2p) and motor impairment on learning and memory performance of wild type and 5xFAD mice on the Morris water maze, from 3 to 15 months of age. The 5xFAD mice showed impaired learning at 6–9 months of age, but memory impairments were not detected with the test procedure used in this study. Performance of 5xFAD mice was profoundly impaired at 12–15 months of age, but was accompanied by slower swim speeds than wild-type mice and a frequent failure to locate the escape platform. Overall female mice performed worse than males, and reversal learning impairments in 5xFAD mice were more pronounced in females than males. Albino mice performed worse than pigmented mice, confirming that albinism can impair performance of 5xFAD mice independently of AD-related transgenes. Overall, these results show that 5xFAD mice have impaired learning performance at 6–9 months of age, but learning and memory performance at 12–15 months is confounded with motor impairments. Furthermore, sex and albinism should be controlled to provide an accurate assessment of AD-related transgenes on learning and memory. These results will help reduce variability across pre-clinical experiments with 5xFAD mice, and thus enhance the reliability of studies developing new therapeutics for AD.

Abstract Image

阿尔茨海默病5xFAD小鼠模型的视觉空间学习和记忆障碍:年龄、性别、白化和运动障碍的影响
5xFAD小鼠阿尔茨海默病(AD)模型迅速发展为AD相关的神经行为病理。然而,5xFAD小鼠的学习和记忆障碍并不总是被复制,在不同的研究中,损伤的大小差异很大。为了研究这种变异的可能来源,我们分析了年龄、性别、背景基因(Tyrc、Oca2p)导致的白化病和运动障碍对野生型和5xFAD小鼠在莫里斯水迷宫中的学习和记忆表现的影响,时间为3至15个月。5xFAD小鼠在6-9个月大时表现出学习障碍,但在本研究中使用的测试程序中未检测到记忆障碍。5xFAD小鼠在12-15月龄时表现严重受损,但游泳速度比野生型小鼠慢,并且经常找不到逃生平台。总体而言,雌性小鼠的表现比雄性小鼠差,5xFAD小鼠的逆转学习障碍在雌性中比雄性更为明显。白化病小鼠的表现比色素小鼠差,证实白化病可以独立于ad相关转基因损害5xFAD小鼠的表现。总体而言,这些结果表明5xFAD小鼠在6-9月龄时学习表现受损,但在12-15月龄时学习和记忆表现与运动障碍相混淆。此外,应控制性别和白化病,以便准确评估ad相关转基因对学习和记忆的影响。这些结果将有助于减少5xFAD小鼠临床前实验的变异性,从而提高开发AD新疗法的研究的可靠性。
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来源期刊
Genes Brain and Behavior
Genes Brain and Behavior 医学-行为科学
CiteScore
6.80
自引率
4.00%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Genes, Brain and Behavior was launched in 2002 with the aim of publishing top quality research in behavioral and neural genetics in their broadest sense. The emphasis is on the analysis of the behavioral and neural phenotypes under consideration, the unifying theme being the genetic approach as a tool to increase our understanding of these phenotypes. Genes Brain and Behavior is pleased to offer the following features: 8 issues per year online submissions with first editorial decisions within 3-4 weeks and fast publication at Wiley-Blackwells High visibility through its coverage by PubMed/Medline, Current Contents and other major abstracting and indexing services Inclusion in the Wiley-Blackwell consortial license, extending readership to thousands of international libraries and institutions A large and varied editorial board comprising of international specialists.
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