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Latency to startle is increased in the 5xFAD mouse model of Alzheimer’s disease.
- Source :
-
Behavioural brain research [Behav Brain Res] 2019 Feb 01; Vol. 359, pp. 823-827. Date of Electronic Publication: 2018 Jul 25. - Publication Year :
- 2019
-
Abstract
- Alzheimer's disease (AD) is a progressive neurodegenerative disorder that results in cognitive decline and a number of other neuropsychiatric symptoms. One area that is often affected by neuropsychiatric disease is the response to sudden, loud noises, as measured by the acoustic startle response (ASR), and prepulse inhibition (PPI), which indicates sensory-gating abilities. Evidence suggests AD patients, even early in the disease, show alteration in ASR. Studies have also shown changes in this measure in transgenic mouse models of AD. To assess the homology of 5xFAD mice to AD patients, the current study analyzed several aspects of the startle response in these mice using a protocol with fewer trials than previous studies. It was found that the 5xFAD mice had a delayed startle response, similar to what has been observed in AD sufferers. These results suggest the ASR may be a useful tool in assessing the efficacy of potential therapeutics, and that a simplified protocol may be more sensitive to between-groups differences for this task.<br /> (Copyright © 2018 Elsevier B.V. All rights reserved.)
- Subjects :
- Acoustic Stimulation
Alzheimer Disease genetics
Amyloid beta-Protein Precursor genetics
Amyloid beta-Protein Precursor metabolism
Animals
Disease Models, Animal
Exploratory Behavior
Habituation, Psychophysiologic genetics
Mice
Mice, Inbred C57BL
Mice, Transgenic
Mutation genetics
Presenilin-1 genetics
Reflex, Startle genetics
Statistics, Nonparametric
Alzheimer Disease physiopathology
Prepulse Inhibition genetics
Reaction Time genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7549
- Volume :
- 359
- Database :
- MEDLINE
- Journal :
- Behavioural brain research
- Publication Type :
- Academic Journal
- Accession number :
- 30055208
- Full Text :
- https://doi.org/10.1016/j.bbr.2018.07.021