Literature DB >> 15219712

Use of multimetric statistical analysis to characterize and discriminate between the performance of four Alzheimer's transgenic mouse lines differing in Abeta deposition.

Ralph E Leighty1, Lars N G Nilsson, Huntington Potter, David A Costa, Mark A Low, Kelly R Bales, Steven M Paul, Gary W Arendash.   

Abstract

Behavioral assessment of genetically-manipulated mouse lines for Alzheimer's disease has become an important index for determining the efficacy of therapeutic interventions and examining disease pathogenesis. However, the potential for higher level statistical analyses to assist in these goals remains largely unexplored. The present study thus involved multimetric statistical analyses of behavioral and beta-amyloid (Abeta) deposition measures from four PDAPP-derived transgenic mouse lines that differ in extent of Abeta deposition. For all four lines, multiple behavioral measures obtained from a comprehensive task battery administered at 15-16 months of age were collectively examined by correlation, factor, and discriminant function analyses. In addition, both compact and total beta-amyloid (Abeta) histologic measures were determined from the same animals. Widespread intra- and inter-task correlations were evident, with impairment in all three water tasks (Morris maze, platform recognition, and radial arm water maze) correlating extensively with Abeta deposition in hippocampus and cerebral cortex. By elucidating the underlying relationships among measures, factor analysis revealed a single primary factor (Factor 1) that loaded most cognitive measures, particularly those for working memory and recognition. Abeta deposition measures loaded exclusively on this primary factor. In individual animals, only factor scores derived from this primary factor were correlated with Abeta deposition. Both of these findings again underscore the association between cognitive impairment and Abeta deposition. Finally, discriminant function analysis (step-wise forward method) was able to distinguish between all four AD transgenic lines based on behavioral performance alone, as well as when Abeta deposition measures were included. Our results demonstrate the utility of higher level, multimetric analysis of behavioral measures from AD transgenic mice. Analyses such as these will be very beneficial for the functional evaluation of therapeutic interventions against AD and for finding behavioral measures that can serve as predictors of pathology.

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Year:  2004        PMID: 15219712     DOI: 10.1016/j.bbr.2003.11.004

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  12 in total

Review 1.  Dissecting the age-related decline on spatial learning and memory tasks in rodent models: N-methyl-D-aspartate receptors and voltage-dependent Ca2+ channels in senescent synaptic plasticity.

Authors:  Thomas C Foster
Journal:  Prog Neurobiol       Date:  2012-01-28       Impact factor: 11.685

2.  Biochemical and behavioral characterization of the double transgenic mouse model (APPswe/PS1dE9) of Alzheimer's disease.

Authors:  Huaqi Xiong; Debbie Callaghan; Jolanta Wodzinska; Jiejing Xu; Maryna Premyslova; Qing-Yan Liu; John Connelly; Wandong Zhang
Journal:  Neurosci Bull       Date:  2011-08       Impact factor: 5.203

3.  Alterations in synaptic plasticity coincide with deficits in spatial working memory in presymptomatic 3xTg-AD mice.

Authors:  Jason K Clark; Matthew Furgerson; Jonathon D Crystal; Marcus Fechheimer; Ruth Furukawa; John J Wagner
Journal:  Neurobiol Learn Mem       Date:  2015-09-15       Impact factor: 2.877

4.  Enhanced cognitive activity--over and above social or physical activity--is required to protect Alzheimer's mice against cognitive impairment, reduce Abeta deposition, and increase synaptic immunoreactivity.

Authors:  Jennifer R Cracchiolo; Takashi Mori; Stanley J Nazian; Jun Tan; Huntington Potter; Gary W Arendash
Journal:  Neurobiol Learn Mem       Date:  2007-08-21       Impact factor: 2.877

5.  Antioxidants and cognitive training interact to affect oxidative stress and memory in APP/PSEN1 mice.

Authors:  F E Harrison; J Allard; R Bixler; C Usoh; L Li; J M May; M P McDonald
Journal:  Nutr Neurosci       Date:  2009-10       Impact factor: 4.994

6.  Caffeine suppresses amyloid-beta levels in plasma and brain of Alzheimer's disease transgenic mice.

Authors:  Chuanhai Cao; John R Cirrito; Xiaoyang Lin; Li Wang; Lilly Wang; Deborah K Verges; Alexander Dickson; Malgorzata Mamcarz; Chi Zhang; Takashi Mori; Gary W Arendash; David M Holtzman; Huntington Potter
Journal:  J Alzheimers Dis       Date:  2009       Impact factor: 4.472

7.  Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit.

Authors:  Gary W Arendash; Takashi Mori; Maggie Dorsey; Rich Gonzalez; Naoki Tajiri; Cesar Borlongan
Journal:  PLoS One       Date:  2012-04-25       Impact factor: 3.240

8.  Functional Dissociation of Group III Metabotropic Glutamate Receptors Revealed by Direct Comparison between the Behavioral Profiles of Knockout Mouse Lines.

Authors:  Hannelore Goddyn; Zsuzsanna Callaerts-Vegh; Rudi D'Hooge
Journal:  Int J Neuropsychopharmacol       Date:  2015-05-21       Impact factor: 5.176

9.  Characterizing cognitive aging of spatial and contextual memory in animal models.

Authors:  Thomas C Foster; R A Defazio; Jennifer L Bizon
Journal:  Front Aging Neurosci       Date:  2012-09-12       Impact factor: 5.750

10.  Cell therapy: a safe and efficacious therapeutic treatment for Alzheimer's disease in APP+PS1 mice.

Authors:  Neel R Nabar; Fang Yuan; Xiaoyang Lin; Li Wang; Ge Bai; Jonathan Mayl; Yaqiong Li; Shu-Feng Zhou; Jinhuan Wang; Jianfeng Cai; Chuanhai Cao
Journal:  PLoS One       Date:  2012-12-03       Impact factor: 3.240

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