Effects of neuromedin U-8 on stress responsiveness and hypothalamus-pituitary-adrenal axis activity in male C57BL/6J mice.
Animals
Arcuate Nucleus of Hypothalamus
/ drug effects
Corticosterone
/ blood
Hypothalamo-Hypophyseal System
/ drug effects
Hypothalamus
/ drug effects
Male
Mice
Mice, Inbred C57BL
Neuropeptides
/ pharmacology
Pituitary-Adrenal System
/ drug effects
Stress, Psychological
/ blood
Swimming
/ psychology
Arcuate nucleus (ARC)
C-Fos immunoreactivity
Forced swim test
Hypothalamus-pituitary-adrenal axis
Neuromedin U (NMU)
Paraventricular nucleus (PVH)
Stress-related behavior
Journal
Hormones and behavior
ISSN: 1095-6867
Titre abrégé: Horm Behav
Pays: United States
ID NLM: 0217764
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
31
07
2019
revised:
29
11
2019
accepted:
24
12
2019
pubmed:
4
1
2020
medline:
7
1
2021
entrez:
4
1
2020
Statut:
ppublish
Résumé
Neuromedin U (NMU) is a highly conserved neuropeptide that has been implicated in the stress response. To better understand how it influences various aspects of the stress response, we studied the effects of intracerebroventricular NMU-8 administration on stress-related behavior and activity of the hypothalamus-pituitary-adrenal (HPA) axis in male C57BL/6J mice. We investigated these NMU-8 effects when mice remained in their home cage and when they were challenged by exposure to forced swim stress. NMU-8 administration resulted in increased grooming behavior in mice that remained in their home cage and in a significant increase in c-Fos immunoreactivity in the paraventricular hypothalamus (PVH) and arcuate nucleus (ARC). Surprisingly, NMU-8 administration significantly decreased plasma corticosterone concentrations. Furthermore, NMU-8 administration increased immobility in the forced swim test in both naïve mice and mice that were previously exposed to swim stress. The effect of NMU-8 on c-Fos immunoreactivity in the PVH was dependent on previous exposure to swim stress given that we observed no significant changes in mice exposed for the first time to swim stress. In contrast, in the ARC we observed a significant increase in c-Fos immunoreactivity regardless of previous stress exposure. Interestingly, NMU-8 administration also significantly decreased plasma corticosterone concentrations in mice that were exposed to single forced swim stress, while this effect was no longer observed when mice were exposed to forced swim stress for a second time. Taken together, our data indicate that NMU-8 regulates stress responsiveness and suggests that its effects depend on previous stress exposure.
Identifiants
pubmed: 31899262
pii: S0018-506X(19)30473-8
doi: 10.1016/j.yhbeh.2019.104666
pii:
doi:
Substances chimiques
Neuropeptides
0
neuromedin U 8
98530-27-9
Corticosterone
W980KJ009P
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
104666Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest None.