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Research article summary (published 30 Jul 2008):

An increase in Abeta42 in the prefrontal cortex is associated with a reversal-learning impairment in Alzheimer's disease model Tg2576 APPsw mice.

Full Abstract

The medial temporal lobe-dependent memory loss associated with Alzheimer's disease (AD) is often accompanied by a loss of prefrontal cortex-dependent cognitive domains that fall under the broad category of executive function. In this study, we examined the relationship between one type of prefrontal-dependent executive function, discrimination reversal-learning, and levels of the amyloid beta protein (Abeta) of 40 and 42 residues in a transgenic mouse model (Tg2576) of the over-expression of the familial AD mutant form of the amyloid precursor protein (APPsw). Tg2576 and their non-transgenic (NTg) littermates were assessed at 3 and 6 months of age when there is little to no amyloid plaque deposition. After reversal-learning assessment, Abeta40 and Abeta42 were quantified in the prefrontal cortex and hippocampus. Tg2576 mice were impaired in reversal-learning at 6 but not 3 months of age when compared to the NTg group. Coincidently, there was a corresponding approximately 3-fold increase of Abeta42 levels in the prefrontal cortex of 6- compared to 3-month-old Tg2576 mice. In addition, the prefrontal cortex contained higher levels of Abeta42 compared to the hippocampus at both 3 and 6 months of age, regardless of genotype, indicating a high vulnerability of this brain region to Abeta42 accumulation. These data suggest that the early emergence of reversal-learning deficits in the Tg2576 mouse may be due to the localized increase of Abeta42 in the prefrontal cortex.

 

Author information

Author/s: Zhuo, Jia-Min (JM); Prakasam, Annamalai (A); Murray, Melissa E (ME); Zhang, Hai-Yan (HY); Baxter, Mark G (MG); Sambamurti, Kumar (K); Nicolle, Michelle M (MM);

Affiliation: Mayo Clinic College of Medicine, Jacksonville, FL, USA.

Grants: R01AG023055 (Agency:NIA NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal: Current Alzheimer research (Curr Alzheimer Res), published in United Arab Emirates. (Language: eng)

Reference: 2008-Aug; vol 5 (issue 4) : pp 385-91

Dates: Created 2008/08/11; Completed 2008/10/14;

PMID: 18690835, status: MEDLINE (last retrieved date: 2/18/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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Associated Chemicals: Amyloid beta-Protein (0) ; Amyloid beta-Protein Precursor (0) ; Peptide Fragments (0) ; amyloid beta-protein (1-42) (0)

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