A touch screen-automated cognitive test battery reveals impaired attention, memory abnormalities, and increased response inhibition in the TgCRND8 mouse model of Alzheimer's disease

被引:81
|
作者
Romberg, Carola [1 ]
Horner, Alexa E. [1 ]
Bussey, Timothy J. [1 ,2 ,3 ]
Saksida, Lisa M. [1 ,2 ,3 ]
机构
[1] Univ Cambridge, Dept Expt Psychol, Cambridge CB2 3EB, England
[2] Univ Cambridge, Wellcome Trust, Cambridge, England
[3] Univ Cambridge, MRC, Behav & Clin Neurosci Inst, Cambridge, England
基金
英国惠康基金;
关键词
Alzheimer's disease; Mouse models; Attention; Response control; Touchscreen; Memory; Cognition; beta-amyloid; TgCRND8; REACTION-TIME-TASK; SHORT-TERM-MEMORY; OBJECT RECOGNITION; TRANSGENIC MICE; NEUROFIBRILLARY CHANGES; SELECTIVE ATTENTION; HIPPOCAMPAL-LESIONS; PERCEPTUAL ODDITY; DEMENTIA; DEFICITS;
D O I
10.1016/j.neurobiolaging.2012.08.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Transgenic mouse models of Alzheimer's disease (AD) with abundant beta-amyloid develop memory impairments. However, multiple nonmnemonic cognitive domains such as attention and executive control are also compromised early in AD individuals, but have not been routinely assessed in animal models. Here, we assessed the cognitive abilities of TgCRND8 mice-a widely used model of beta-amyloid pathology-with a touch screen-based automated test battery. The test battery comprises highly translatable tests of multiple cognitive constructs impaired in human AD, such as memory, attention, and response control, as well as appropriate control tasks. We found that familial AD mutations affect not only memory, but also cause significant alterations of sustained attention and behavioral flexibility. Because changes in attention and response inhibition may affect performance on tests of other cognitive abilities including memory, our findings have important consequences for the assessment of disease mechanisms and therapeutics in animal models of AD. A more comprehensive phenotyping with specialized, multicomponent cognitive test batteries for mice might significantly advance translation from preclinical mouse studies to the clinic. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:731 / 744
页数:14
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