Abstract

RationaleThe CANTAB object-location paired-associate learning (PAL) test can detect cognitive deficits in schizophrenia and Alzheimer’s disease. A rodent version of touch screen PAL (dPAL) has been developed, but the underlying neural mechanisms are not fully understood. Although there is evidence that inactivation of the hippocampus following training leads to impairments in rats, this has not been tested in mice. Furthermore, it is not known whether acquisition, as opposed to performance, of the rodent version depends on the hippocampus. This is critical as many mouse models may have hippocampal dysfunction prior to the onset of task training.ObjectivesThe objectives of this study are to examine the effects of dorsal hippocampal (dHp) dysfunction on both performance and acquisition of mouse dPAL and to determine if hippocampal task sensitivity could be increased using a newly developed context-disambiguated PAL (cdPAL) paradigm.MethodsIn experiment 1, C57Bl/6 mice received post-acquisition dHp infusions of the GABA agonist muscimol. In experiment 2, C57Bl/6 mice received excitotoxic dHp lesions prior to dPAL/cdPAL acquisition.ResultsPost-acquisition muscimol dose-dependently impaired dPAL and cdPAL performance. Pre-acquisition dHp lesions had only mild effects on both PAL tasks. Behavioural challenges including addition of objects and degradation of the visual stimuli with noise did not reveal any further impairments.ConclusionsdPAL and cdPAL performance is hippocampus-dependent in the mouse, but both tasks can be learned in the absence of a functional dHp.

Highlights

  • Object-location paired-associate learning (PAL) as tested in the touch screen CANTAB battery is highly sensitive to impairment in Alzheimer’s disease (AD) and schizophrenia yet is not disrupted in conditions such as depression (Swainson et al 2001), thereby conveying good task specificity

  • In parallel with these experiments, we developed a new version of mouse PAL (context-disambiguated PAL), in which visual stimuli were presented in two physically separated areas in the touch screen chamber, to test whether presenting stimuli in two contexts would increase task hippocampal sensitivity

  • In the context-disambiguated PAL (cdPAL) task, reward collection latency was significantly larger after muscimol infusion (F(2,20)=8.04, p=0.003) and pairwise comparison with Bonferroni correction showed that the difference was between vehicle and high dose (0.1 μg/mouse) but not in any other comparison

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Summary

Introduction

Object-location paired-associate learning (PAL) as tested in the touch screen CANTAB battery is highly sensitive to impairment in Alzheimer’s disease (AD) and schizophrenia yet is not disrupted in conditions such as depression (Swainson et al 2001), thereby conveying good task specificity. In AD, PAL is highly sensitive to disease progression (Fowler et al 2002), and a short tablet computer-based assessment tool based on this task has recently been made available to general practitioners in the UK to help with dementia detection (Todd 2013; Cambridge Cognition 2014). A version of object-location PAL for rodent models of disease (dPAL) has been developed in the touch screen operant behavioural system. To date, it has been validated in rats (Talpos et al 2009; McAllister et al in this issue) and used to assess cognitive deficits in genetically modified mice (Bartko et al 2011a; Coba et al 2012; Nithianantharajah et al 2013). The full translational potential of this task was recently demonstrated in a study showing parallel cognitive

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