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Impaired Reversal Learning in APPPS1-21 Mice in the Touchscreen Visual Discrimination Task

机译:触摸屏视觉识别任务中APPPS1-21小鼠的逆向学习受损。

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摘要

Preclinical-clinical translation of cognitive functions has been difficult in Alzheimer’s disease (AD) research but is crucial to the (predictive) validity of AD animal models. Reversal learning, a representation of flexibility and adaptability to a changing environment, might represent such a translatable feature of human cognition. We, therefore, examined visual discrimination (VD) and reversal learning in the APPPS1-21 mouse model of amyloid-based AD pathology. We used touchscreen operant cages in novel and translationally valid, as well as objective testing methodology that minimizes within- or between-trial handling. Mice were trained to associate a visual cue with a food reward (VD learning), and subsequently learned to adjust their response when this rule changed (reversal learning). We assessed performance at two different ages, namely at 6 months of age, considered an early disease stage, and at 9 months, a stage of established pathology. Both at 6 and 9 months, transgenic animals needed more sessions to reach criterion performance, compared to wild-type controls. Overall, transgenic animals do not show a general cognitive, motivational or motor deficit, but experience specific difficulties to adapt to reward contingency changes, already at an early pathology stage.
机译:在阿尔茨海默氏病(AD)研究中,认知功能的临床前到临床翻译一直很困难,但对于AD动物模型的(预测)有效性至关重要。逆向学习是对不断变化的环境的灵活性和适应性的代表,它可以代表人类认知的这种可翻译特征。因此,我们在基于淀粉样蛋白的AD病理的APPPS1-21小鼠模型中检查了视觉辨别力(VD)和逆向学习。我们在新颖且具有翻译效力的触摸屏操作笼中使用了客观的测试方法,从而最大程度地减少了审判内或审判间的处理。对小鼠进行了训练,使视觉提示与食物奖励相关联(VD学习),随后在规则改变时学会了调整其反应(逆向学习)。我们评估了两个不同年龄的表现,即在6个月大的阶段(被认为是疾病的早期阶段)和9个月大的病理阶段。与野生型对照相比,在6个月和9个月时,转基因动物都需要更多的时间来达到标准性能。总体而言,转基因动物没有表现出普遍的认知,动机或运动缺陷,但是在病理早期已经经历了适应奖励偶然性变化的特殊困难。

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