Memory generalization after one-trial contextual fear conditioning: Effects of sex and neuropeptide S receptor deficiency.


Journal

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

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 22 11 2018
revised: 18 12 2018
accepted: 27 12 2018
pubmed: 1 1 2019
medline: 5 6 2019
entrez: 1 1 2019
Statut: ppublish

Résumé

One-trial contextual fear conditioning in laboratory mice results in a fear memory which is relatively specific to the original conditioning context shortly after conditioning but becomes more unspecific after an incubation time of one month. This process is called generalization of fear memory and is used to investigate processes which might be involved in the pathogenesis of post-traumatic stress disorder. In the present study, we investigated the effects of sex and neuropeptide S receptor (NPSR) deficiency in one-trial contextual fear conditioning. In addition to contextual fear, we also measured startle reactivity, anxiety and corticosterone plasma levels of the mice. Our data show main effects of sex and NPSR-deficiency on freezing behavior, startle magnitude, and anxiety levels. However, generalization of contextual fear memory after incubation time was not affected by sex. Notably, NPSR-deficient mice had a more specific fear memory shortly after conditioning than their wildtype littermates but after incubation time, all genotypes had a generalized fear memory. The present data further show that plasma corticosterone levels are increased after incubation time. This increase was significantly more pronounced in NPSR-deficient mice. Taken together, our study confirms the suitability of one-trial contextual fear conditioning to study the effects of incubation time on fear memory generalization but also indicates the need for control groups without incubation. We further demonstrate that the increase of plasma corticosterone levels after incubation time is exaggerated in NPSR-deficient mice. The latter finding suggests an important role of the NPS system in the regulation of corticosterone release.

Identifiants

pubmed: 30597251
pii: S0166-4328(18)31641-3
doi: 10.1016/j.bbr.2018.12.046
pii:
doi:

Substances chimiques

NPSR1 protein, mouse 0
Receptors, G-Protein-Coupled 0
Corticosterone W980KJ009P

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-166

Informations de copyright

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

Auteurs

Josephine Germer (J)

Institute for Pharmacology and Toxicology, Otto-von-Guericke University Magdeburg, Leipziger Straße 44, D-39120 Magdeburg, Germany.

Evelyn Kahl (E)

Institute for Pharmacology and Toxicology, Otto-von-Guericke University Magdeburg, Leipziger Straße 44, D-39120 Magdeburg, Germany.

Markus Fendt (M)

Institute for Pharmacology and Toxicology, Otto-von-Guericke University Magdeburg, Leipziger Straße 44, D-39120 Magdeburg, Germany; Center for Behavioral Brain Sciences, Otto-von-Guericke University Magdeburg, Leipziger Straße 44, D-39120 Magdeburg, Germany. Electronic address: markus.fendt@med.ovgu.de.

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Classifications MeSH