Prolonged isolation stress accelerates the onset of Alzheimer's disease-related pathology in 5xFAD mice despite running wheels and environmental enrichment.


Journal

Behavioural brain research
ISSN: 1872-7549
Titre abrégé: Behav Brain Res
Pays: Netherlands
ID NLM: 8004872

Informations de publication

Date de publication:
03 02 2020
Historique:
received: 28 05 2019
revised: 14 11 2019
accepted: 14 11 2019
pubmed: 20 11 2019
medline: 4 5 2021
entrez: 20 11 2019
Statut: ppublish

Résumé

Research has demonstrated that stress can exacerbate AD pathology in transgenic mouse models of AD. The purpose of the present studies was to extend this work by determining whether a social stressor, isolation stress, would increase the number of Aβ plaques in 5xFAD + transgenic mice in comparison to group-housed controls, and accelerate the onset of cognitive deficits in contextual fear-conditioning. Additionally, we aimed to determine whether the pathological impact of isolation stress could be prevented through exposure to exercise alone or to exercise and an enriched environment throughout the isolation period. Two-month-old 5xFAD + and 5xFAD- animals were isolated or group-housed for two and three months. An additional subset of 5xFAD + mice were housed in isolation, housed in isolation with an exercise wheel, or housed in isolation with an exercise wheel and an enriched environment. Both two and three months of isolation stress significantly increased the number of plaques in the hippocampus of 5xFAD + mice, and three months of isolation increased hippocampal BACE1 expression. Isolated animals also displayed a significant cognitive deficit in contextual fear-conditioning, independent of genotype. Furthermore, neither exercise nor an enriched environment were able to prevent these isolation-induced effects. Understanding how stress impacts the onset and progression of AD is critical, as many individuals endure significant stress over their lifespan, including prolonged social isolation, a societal trend likely to worsen with time.

Identifiants

pubmed: 31743728
pii: S0166-4328(19)30835-6
doi: 10.1016/j.bbr.2019.112366
pii:
doi:

Substances chimiques

Amyloid beta-Peptides 0
Amyloid Precursor Protein Secretases EC 3.4.-
Aspartic Acid Endopeptidases EC 3.4.23.-
Bace1 protein, mouse EC 3.4.23.46

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

112366

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

J L Peterman (JL)

Department of Psychology, Texas Christian University, United States.

J D White (JD)

Department of Psychology, Texas Christian University, United States.

A Calcagno (A)

Department of Psychology, Texas Christian University, United States.

C Hagen (C)

Department of Biology, Texas Christian University, United States.

M Quiring (M)

Department of Biology, Texas Christian University, United States.

K Paulhus (K)

Department of Biology, Texas Christian University, United States.

T Gurney (T)

Department of Biology, Texas Christian University, United States.

M J Eimerbrink (MJ)

Department of Psychology, Texas Christian University, United States.

M Curtis (M)

Department of Biology, Texas Christian University, United States.

G W Boehm (GW)

Department of Psychology, Texas Christian University, United States.

M J Chumley (MJ)

Department of Biology, Texas Christian University, United States. Electronic address: m.chumley@tcu.edu.

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Classifications MeSH