Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20970
Title: Evaluation of attention in APP/PS1 mice reveals impulsive and compulsive behaviours.
Austin Authors: Shepherd, A;May, C;Churilov, Leonid ;Adlard, P A;Hannan, A J;Burrows, E L
Affiliation: Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC 3010, Australia
The Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia
Florey Institute of Neuroscience and Mental Health, Kenneth Myer Building, University of Melbourne, Parkville, VIC 3052, Australia
Issue Date: 8-Jun-2019
metadata.dc.date: 2019-06-08
Publication information: Genes, brain, and behavior 2019: e12594
Abstract: While Alzheimer's disease (AD) is traditionally associated with deficits in episodic memory, early changes in other cognitive domains, such as attention, have been gaining interest. In line with clinical observations, some animal models of AD have been shown to develop attentional deficits, but this is not consistent across all models. The APPswe/PS1∆E9 (APP/PS1) mouse is one of the most commonly used AD models and attention has not yet been scrutinised in this model. We set out to assess attention using the 5-choice serial reaction time task (5CSRTT) early in the progression of cognitive symptoms in APP/PS1 mice, using clinically translatable touchscreen chambers. APP/PS1 mice showed no attentional changes across 5CSRTT training or any probes from 9-11 months of age. Interestingly, APP/PS1 mice showed increased impulsive and compulsive responding when task difficulty was high. This suggests that while the APP/PS1 mouse model may not be a good model of attentional changes in AD, it may be useful to study the early changes in impulsive and compulsive behaviour that have been identified in patient studies. As these changes have not previously been reported without attentional deficits in the clinic, the APP/PS1 mouse model may provide a unique opportunity to study these specific behavioural changes seen in AD, including their mechanistic underpinnings and therapeutic implications.
URI: http://ahro.austin.org.au/austinjspui/handle/1/20970
DOI: 10.1111/gbb.12594
ORCID: 0000-0002-6675-4679
0000-0002-9807-6606
PubMed URL: 31177612
Type: Journal Article
Appears in Collections:Journal articles

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