Mid-Adulthood Cognitive Training Improves Performance in a Spatial Task but Does Not Ameliorate Hippocampal Pathology in a Mouse Model of Alzheimer's Disease

被引:3
作者
Williams, Elizabeth [1 ]
Alex, Ashli [1 ]
Chin, Xi Wei [1 ]
Spires-Jones, Tara [2 ]
Wang, Szu-Han [1 ]
机构
[1] Univ Edinburgh, Ctr Clin Brain Sci, 49 Little France Crescent, Edinburgh EH16 4SB, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Discovery Brain Sci, UK Dementia Res Inst, Edinburgh, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Aging; Alzheimer's disease; amyloid-beta; astrocytes; cognitive reserve; dementia; hippocampus; BETA-AMYLOID DEPOSITION; APP/PS1 TRANSGENIC MICE; MORRIS WATER MAZE; MEMORY DEFICITS; BEHAVIORAL-CHANGES; TAU-PATHOLOGY; A-BETA; EXERCISE; NMDA; RECEPTORS;
D O I
10.3233/JAD-221185
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Prior experience in early life has been shown to improve performance in aging and mice with Alzheimer's disease (AD) pathology. However, whether cognitive training at a later life stage would benefit subsequent cognition and reduce pathology in AD mice needs to be better understood. Objective: This study aimed to verify if behavioral training in mid-adulthood would improve subsequent cognition and reduce AD pathology and astrogliosis. Methods: Mixed-sex APP/PS1 and wildtype littermate mice received a battery of behavioral training, composed of spontaneous alternation in the Y-maze, novel object recognition and location tasks, and spatial training in the water maze, or handling only at 7 months of age. The impact of AD genotype and prior training on subsequent learning and memory of aforementioned tasks were assessed at 9 months. Results: APP/PS1 mice made more errors than wildtype littermates in the radial-armwater maze (RAWM) task. Prior training prevented this impairment in APP/PS1 mice. Prior training also contributed to better efficiency in finding the escape platform in both APP/PS1 mice and wildtype littermates. Short-term and long-term memory of this RAWMtask, of a reversal task, and of a transfer task were comparable among APP/PS1 and wildtype mice, with or without prior training. Amyloid pathology and astrogliosis in the hippocampus were also comparable between the APP/PS1 groups. Conclusion: These data suggest that cognitive training in mid-adulthood improves subsequent accuracy in AD mice and efficiency in all mice in the spatial task. Cognitive training in mid-adulthood provides no clear benefit on memory or on amyloid pathology in midlife.
引用
收藏
页码:683 / 704
页数:22
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