School of Life Sciences, Faculty of Science, University of Technology Sydney, Sydney, New South Wales 2007, Australia.
Centre for Neuroscience and Regenerative Medicine, St. Vincent's Centre for Applied Medical Research, St. Vincent's Health Network, Sydney, New South Wales 2010, Australia.
eNeuro. 2023 Feb 13;10(2). doi: 10.1523/ENEURO.0363-22.2023. Print 2023 Feb.
Cognitive-behavioral testing in preclinical models of Alzheimer's disease has failed to capture deficits in goal-directed action control. Here, we provide the first comprehensive investigation of goal-directed action in a transgenic mouse model of Alzheimer's disease. Specifically, we tested outcome devaluation performance in male and female human amyloid precursor protein (hAPP)-J20 mice. Mice were first trained to press left and right levers for pellet and sucrose outcomes, respectively (counterbalanced), over 4 d. On test, mice were prefed one of the outcomes to satiety and given a choice between levers. Devaluation performance was intact for 36-week-old wild-types of both sexes, who responded more on the valued relative to the devalued lever (Valued > Devalued). By contrast, devaluation was impaired (Valued = Devalued) for J20 mice of both sexes, and for 52-week-old male mice regardless of genotype. After additional lever press training (i.e., 8-d lever pressing in total), devaluation was intact for all mice, demonstrating that the initial deficits were not a result of a nonspecific impairment in reward processing, depression, or locomotor activity in J20 or aging mice. Follow-up analyses revealed that microglial expression in the dorsal CA1 region of the hippocampus was associated with poorer outcome devaluation performance on initial, but not later tests. Together, these data demonstrate that goal-directed action is initially impaired in J20 mice of both sexes and in aging male mice regardless of genotype, and that this impairment is related to neuroinflammation in the dorsal CA1 hippocampal region.
在阿尔茨海默病的临床前模型中的认知行为测试未能捕捉到目标导向动作控制的缺陷。在这里,我们首次全面研究了阿尔茨海默病转基因小鼠模型中的目标导向动作。具体来说,我们测试了雄性和雌性人淀粉样前体蛋白(hAPP)-J20 小鼠的目标导向动作的结果评价表现。首先,在 4 天内,将小鼠训练按压左右杠杆以分别获得颗粒和蔗糖的结果(平衡)。在测试中,将其中一种结果预先喂给小鼠至饱食,并让它们在杠杆之间进行选择。36 周龄的雄性和雌性野生型的结果评价表现完整,他们对有价值的杠杆(Valued > Devalued)的反应比对无价值的杠杆(Valued = Devalued)更多。相比之下,两种性别的 J20 小鼠以及无论基因型如何的 52 周龄雄性小鼠的结果评价都受损。经过额外的杠杆按压训练(即总共 8 天的杠杆按压)后,所有小鼠的结果评价都完整,表明初始缺陷不是由于 J20 或衰老小鼠中特定的奖励处理、抑郁或运动活动受损所致。后续分析表明,海马体背侧 CA1 区的小胶质细胞表达与初始测试而非后续测试中的结果评价表现较差相关。总之,这些数据表明,无论性别和基因型如何,J20 小鼠和老年雄性小鼠的目标导向动作最初都会受损,并且这种损伤与背侧 CA1 海马区的神经炎症有关。