Research Center for Next-Generation Drug Development, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Aichi, 464-8601, Japan.
Department of Neuroscience and Pathobiology, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Aichi, 464-8601, Japan.
Mol Brain. 2020 Nov 13;13(1):147. doi: 10.1186/s13041-020-00690-6.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by cognitive decline with accumulation of amyloid beta (Aβ) and neurofibrillary tangles that usually begins 15-30 years before clinical diagnosis. Rodent models that recapitulate aggressive Aβ and/or the pathology of neurofibrillary tangles are essential for AD research. Accordingly, non-invasive early detection systems in these animal models are required to evaluate the phenotypic changes, elucidate the mechanism of disease progression, and facilitate development of novel therapeutic approaches. Although many behavioral tests efficiently reveal cognitive impairments at the later stage of the disease in AD models, it has been challenging to detect such impairments at the early stage. To address this issue, we subjected 4-6-month-old male App knock-in (App-KI) mice to touchscreen-based location discrimination (LD), different object-location paired-associate learning (dPAL), and reversal learning tests, and compared the results with those of the classical Morris water maze test. These tests are mainly dependent on the brain regions prone to Aβ accumulation at the earliest stages of the disease. At 4-6 months, considered to represent the early stage of disease when mice exhibit initial deposition of Aβ and slight gliosis, the classical Morris water maze test revealed no difference between groups, whereas touchscreen-based LD and dPAL tasks revealed significant impairments in task performance. Our report is the first to confirm that a systematic touchscreen-based behavioral test battery can sensitively detect the early stage of cognitive decline in an AD-linked App-KI mouse model. This system could be applied in future translational research.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是认知能力下降,淀粉样β(Aβ)和神经原纤维缠结积累,通常在临床诊断前 15-30 年开始。重现侵袭性 Aβ和/或神经原纤维缠结病理学的啮齿动物模型对于 AD 研究至关重要。因此,需要在这些动物模型中建立非侵入性的早期检测系统,以评估表型变化、阐明疾病进展的机制,并促进新的治疗方法的开发。虽然许多行为测试在 AD 模型的疾病后期能够有效地揭示认知障碍,但在早期阶段检测到这些障碍一直具有挑战性。为了解决这个问题,我们对 4-6 个月大的雄性 APP 基因敲入(App-KI)小鼠进行了基于触摸屏的位置辨别(LD)、不同物体-位置配对联想学习(dPAL)和反转学习测试,并将结果与经典的 Morris 水迷宫测试进行了比较。这些测试主要依赖于疾病早期最容易积聚 Aβ的大脑区域。在 4-6 个月时,被认为是疾病的早期阶段,此时小鼠表现出初始 Aβ沉积和轻微神经胶质增生,经典的 Morris 水迷宫测试显示组间无差异,而基于触摸屏的 LD 和 dPAL 任务则显示出任务表现的显著损伤。我们的报告首次证实,系统的基于触摸屏的行为测试组合可以敏感地检测到 AD 相关 App-KI 小鼠模型中认知衰退的早期阶段。该系统可应用于未来的转化研究。