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Article type: Research Article
Authors: Williams, Elizabetha; 1 | Mutlu-Smith, Menekşea; 1 | Alex, Ashlia; 2 | Chin, Xi Weia; 2 | Spires-Jones, Tarab | Wang, Szu-Hana; *
Affiliations: [a] Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK | [b] Centre for Discovery Brain Sciences, UK Dementia Research Institute, The University of Edinburgh, Edinburgh, UK
Correspondence: [*] Correspondence to: Szu-Han Wang, Centre for Clinical Brain Sciences, The University of Edinburgh, 49 Little France Crescent, Edinburgh BioQuarter, Edinburgh, EH16 4SB, UK. E-mail: s.wang@ed.ac.uk.
Note: [1] These authors contributed equally to this work.
Note: [2] These authors contributed equally to this work.
Abstract: 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-arm water 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 RAWM task, 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.
Keywords: Aging, Alzheimer’s disease, amyloid-β, astrocytes, cognitive reserve, dementia, hippocampus
DOI: 10.3233/JAD-221185
Journal: Journal of Alzheimer's Disease, vol. 93, no. 2, pp. 683-704, 2023
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