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Neuroscience 2000 Abstract

Presentation Number: 397.6
Abstract Title: Behavioral consequences of vaccination with human β-amyloid in mutant APP + PS1 transgenic mice.
Authors: Arendash, G.*1 ; Hatcher, J.1 ; Canals, K.2 ; Diamond, D. M.2 ; Gottschall, P.3 ; Gordon, M.3 ; Morgan, D.3
1Depts. of Biology, University of South Florida, Tampa, FL
2Psychology, University of South Florida, Tampa, FL
3and Pharmacology, University of South Florida, Tampa, FL

Primary Theme and Topics J. Disorders of the Nervous System and Aging
- 126. Degenerative disease: Alzheimer's-beta amyloid
Secondary Theme and Topics J. Disorders of the Nervous System and Aging<br />- 128. Degenerative disease: Alzheimer's-cognitive function
Session: 397. Degenerative disease: Alzheimer's--beta amyloid: animal models IV
Slide
Presentation Time: Tuesday, November 7, 2000 9:15 AM-9:30 AM
Location: Room 268
Keywords: Cognitive Protection, Innoculation, Beta-Amyloid, Alzheimer's Disease
Recently, vaccination of the PDAPP transgenic mouse with human beta-amyloid (Aβ) peptide was found to prevent or decrease Aβ deposition in the brain (Schenk et al., Nature 400:173, 1999). The present study investigated the behavioral consequences Aβ vaccination in doubly transgenic APP+PS1 mic. These mice are cognitively normal through 6-8 months of age but impaired by 16-17 months (see abstract by A. Campbell et al.), which parallels their progressive increase in brain Aβ deposition. At 8 months of age, doubly transgenic mice (Tg+) and non-transgenic (Tg-) controls began receiving months vaccinations with human Aβ1-42 or KLH control vaccinations. Behavioral testing of Tg+ and Tg- mice at 12 months of age (when blood Aβ antibody titers should be about 1:10,000) revealed no deleterious effects of Aβ vaccination on learning/working memory in the radial arm water maze (RAWM) task. Behavioral results from a follow-up RAWM test at 16 months of age will be presented. Also, human Aβ1-42 vaccination of 14 months old Tg+ mice from a different genetic background (bub strain) had no deleterious effects on a variety of sensorimotor and cognitive tasks; this, despite substantive blood Aβ antibody titers. Our results indicate that Aβ vaccinations in Tg+ mice bearing Aβ deposits do not impair their cognitive performance, thus providing an opportunity for cognitive protection during aging.

Sample Citation:

[Authors]. [Abstract Title]. Program No. XXX.XX. 2000 Neuroscience Meeting Planner. New Orleans, LA: Society for Neuroscience, 2000. Online.

Copyright © 2000-2026 Society for Neuroscience; all rights reserved. Permission to republish any abstract or part of any abstract in any form must be obtained in writing by SfN office prior to publication.

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