Abstract

Using a longitudinal study design, two strains of Alzheimer's disease (AD) model mice, one expressing β-amyloid plaques and one expressing Tau protein-associated neurofibrillary tangles were assessed for olfactory and visuospatial learning and memory and their performance compared to that of age-matched controls. No significant difference between AD and control mice was found in the initial set of olfactory tasks performed at 6 months of age whereas both strains of AD mice performed significantly poorer than the controls in visuospatial learning at this age. Subsequent tests performed on the same individual animals at 7, 8, 9, 11, 13, 15, and 18 months of age also failed to find systematic differences in olfactory performance between AD and control mice. In contrast, the AD mice performed consistently poorer than the controls in visuospatial re-learning tests performed at these ages. With most olfactory tasks, both AD and control mice displayed a marked decrease in performance between testing at 15 and 18 months of age. These results show that the two strains of AD model mice do not display an olfactory impairment in a time course consistent with human AD, but are impaired in visuospatial capabilities. The marked age-related changes observed with the olfactory tasks in both AD and control mice suggest that the observed lack of an AD-related olfactory impairment is not due to an insensitivity of the tests employed. Rather, they suggest that the olfactory system of the two AD mouse model strains may be surprisingly robust against AD-typical neuropathologies.

Highlights

  • Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by progressive cognitive and sensory impairment

  • The causes underlying AD are not fully understood, it is commonly agreed that the accumulation of b-amyloid plaques and Tau protein-associated neurofibrillary tangles in the brain are characteristic for the neuropathology of the disease

  • The two AD model mouse strains used in the present study have been characterized thoroughly with regard to the onset, progression and severity of their neuropathologies [4,5,6,7] and correlations with the sensory and cognitive performance of longitudinally tested animals should be reliable

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Summary

Introduction

Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by progressive cognitive and sensory impairment. The disadvantages of this study design are that it requires a comparatively high number of animals, that measures of long-term re-learning are rather restricted, and the progression of AD- or age-related changes in all measures of performance can only be inferred indirectly - across (rather than within) animals. We consider it useful to complement this approach with studies adopting a longitudinal design, that is, animals are tested repeatedly at several times during their lifespan. The two AD model mouse strains used in the present study have been characterized thoroughly with regard to the onset, progression and severity of their neuropathologies [4,5,6,7] and correlations with the sensory and cognitive performance of longitudinally tested animals should be reliable

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