Novel Behavioural Characteristics of Male Human P301S Mutant Tau Transgenic Mice – A Model for Tauopathy. (1st April 2020)
- Record Type:
- Journal Article
- Title:
- Novel Behavioural Characteristics of Male Human P301S Mutant Tau Transgenic Mice – A Model for Tauopathy. (1st April 2020)
- Main Title:
- Novel Behavioural Characteristics of Male Human P301S Mutant Tau Transgenic Mice – A Model for Tauopathy
- Authors:
- Watt, Georgia
Przybyla, Magdalena
Zak, Valeria
van Eersel, Janet
Ittner, Arne
Ittner, Lars M.
Karl, Tim - Abstract:
- Highlights: TAU58/2 males demonstrated anxiolytic-like but not disinhibitory behaviours. TAU58/2 males show reduced sociability but not increased aggression. TAU58/2 males demonstrate impaired acoustic startle response and prepulse inhibition. Abstract: Alzheimer's disease (AD) is a neurodegenerative disease characterised by progressive cognitive decline and the accumulation of two hallmark proteins, amyloid-beta (Aβ) and tau. Traditionally, transgenic mouse models for AD have generally focused on Aβ pathology, however, in recent years a number of tauopathy transgenic mouse models have been developed, including the TAU58/2 mouse model. These mice develop tau pathology and neurofibrillary tangles from 2 months of age and show motor impairments and alterations in the behavioural response to elevated plus maze (EPM) testing. The cognitive and social phenotype of this model has not yet been assessed comprehensively. Furthermore, the behavioural changes seen in the EPM have previously been linked to both anxiety and disinhibitory phenotypes. Thus, this study assessed 4-month-old TAU58/2 males comprehensively for disinhibitory and social behaviours, social recognition memory, and sensorimotor gating. TAU58/2 males demonstrated reduced exploration and anxiety-like behaviours but no changes to disinhibitory behaviours, reduced sociability in the social preference test and impaired acoustic startle and prepulse inhibition. Aggressive and socio-positive behaviours were not affectedHighlights: TAU58/2 males demonstrated anxiolytic-like but not disinhibitory behaviours. TAU58/2 males show reduced sociability but not increased aggression. TAU58/2 males demonstrate impaired acoustic startle response and prepulse inhibition. Abstract: Alzheimer's disease (AD) is a neurodegenerative disease characterised by progressive cognitive decline and the accumulation of two hallmark proteins, amyloid-beta (Aβ) and tau. Traditionally, transgenic mouse models for AD have generally focused on Aβ pathology, however, in recent years a number of tauopathy transgenic mouse models have been developed, including the TAU58/2 mouse model. These mice develop tau pathology and neurofibrillary tangles from 2 months of age and show motor impairments and alterations in the behavioural response to elevated plus maze (EPM) testing. The cognitive and social phenotype of this model has not yet been assessed comprehensively. Furthermore, the behavioural changes seen in the EPM have previously been linked to both anxiety and disinhibitory phenotypes. Thus, this study assessed 4-month-old TAU58/2 males comprehensively for disinhibitory and social behaviours, social recognition memory, and sensorimotor gating. TAU58/2 males demonstrated reduced exploration and anxiety-like behaviours but no changes to disinhibitory behaviours, reduced sociability in the social preference test and impaired acoustic startle and prepulse inhibition. Aggressive and socio-positive behaviours were not affected except a reduction in the occurrence of nosing and anogenital sniffing . Our study identified new phenotypic characteristics of young adult male TAU58/2 transgenic mice and clarified the nature of changes detected in the behavioural response of these mice to EPM testing. Social withdrawal and inappropriate social behaviours are common symptoms in both AD and FTD patients and impaired sensorimotor gating is seen in moderate-late stage AD, emphasising the relevance of the TAU58/2 model to these diseases. … (more)
- Is Part Of:
- Neuroscience. Volume 431(2020)
- Journal:
- Neuroscience
- Issue:
- Volume 431(2020)
- Issue Display:
- Volume 431, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 431
- Issue:
- 2020
- Issue Sort Value:
- 2020-0431-2020-0000
- Page Start:
- 166
- Page End:
- 175
- Publication Date:
- 2020-04-01
- Subjects:
- AD Alzheimer's disease -- ASR acoustic startle response -- Aβ amyloid-beta -- EPM elevated plus maze -- FTD frontotemporal dementia -- ITI inter-trial interval -- NFTs neurofibrillary tangles -- PPI prepulse inhibition -- SI social interaction -- SPT social preference test
TAU58/2 transgenic mouse -- animal model -- Alzheimer's disease -- behaviour -- tau pathology
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2020.01.047 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.559000
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