Cargando…

Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area

BACKGROUND: Chronic stress-induced depressive-like behavior is relevant to inflammatory immune activation. However, the neurobiological alterations in the brain following the central inflammatory immune activation remain elusive. METHODS: Therefore, we investigated the neurobiological alterations du...

Descripción completa

Detalles Bibliográficos
Autores principales: Sekio, Miyu, Seki, Kenjiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368860/
https://www.ncbi.nlm.nih.gov/pubmed/25539502
http://dx.doi.org/10.1093/ijnp/pyu005
_version_ 1782362703246917632
author Sekio, Miyu
Seki, Kenjiro
author_facet Sekio, Miyu
Seki, Kenjiro
author_sort Sekio, Miyu
collection PubMed
description BACKGROUND: Chronic stress-induced depressive-like behavior is relevant to inflammatory immune activation. However, the neurobiological alterations in the brain following the central inflammatory immune activation remain elusive. METHODS: Therefore, we investigated the neurobiological alterations during depressive-like behavior induced in mice by systemic administration of lipopolysaccharide (LPS; 1.2mg/kg administered twice at a 30-min interval via intraperitoneal injection). RESULTS: At 24h after the second administration of LPS, an increased immobility time in the tail suspension test and the forced swimming test were observed, as well as reduced sucrose preference. Protein levels of the AMPA receptor GluR1 were significantly decreased at the plasma membrane in the medial prefrontal cortex (mPFC) and ventral tegmental area (VTA), while levels of the GluR2 were increased at the plasma membrane in the nucleus accumbens (NAc) at 24h after LPS. However, total GluR1 and GluR2 protein levels in the mPFC, VTA, and NAc were not affected by LPS. Moreover, LPS facilitated release of noradrenaline in the mPFC and VTA, but not in the NAc. Consistently, systemic administration of prazosin, an α(1)-adrenoceptor antagonist, blocked the LPS-induced downregulation of the membrane GluR1 subunit in both the mPFC and VTA and also blocked the upregulation of the membrane GluR2 subunit in the NAc. Intracerebroventricular administration of prazosin 30min before LPS injection abrogated the LPS-induced depressive-like behaviors. In opposition, administration of propranolol, a β-adrenoceptor antagonist, did not affect the LPS-induced downregulation of GluR1, the upregulation of GluR2, or the depressive-like behavior. CONCLUSIONS: These results suggest that LPS-activated α(1)-adrenoceptor-induced downregulation of membrane GluR1 in the mPFC and VTA is associated with inflammation-induced depressive-like behavior.
format Online
Article
Text
id pubmed-4368860
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-43688602015-09-01 Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area Sekio, Miyu Seki, Kenjiro Int J Neuropsychopharmacol Research Article BACKGROUND: Chronic stress-induced depressive-like behavior is relevant to inflammatory immune activation. However, the neurobiological alterations in the brain following the central inflammatory immune activation remain elusive. METHODS: Therefore, we investigated the neurobiological alterations during depressive-like behavior induced in mice by systemic administration of lipopolysaccharide (LPS; 1.2mg/kg administered twice at a 30-min interval via intraperitoneal injection). RESULTS: At 24h after the second administration of LPS, an increased immobility time in the tail suspension test and the forced swimming test were observed, as well as reduced sucrose preference. Protein levels of the AMPA receptor GluR1 were significantly decreased at the plasma membrane in the medial prefrontal cortex (mPFC) and ventral tegmental area (VTA), while levels of the GluR2 were increased at the plasma membrane in the nucleus accumbens (NAc) at 24h after LPS. However, total GluR1 and GluR2 protein levels in the mPFC, VTA, and NAc were not affected by LPS. Moreover, LPS facilitated release of noradrenaline in the mPFC and VTA, but not in the NAc. Consistently, systemic administration of prazosin, an α(1)-adrenoceptor antagonist, blocked the LPS-induced downregulation of the membrane GluR1 subunit in both the mPFC and VTA and also blocked the upregulation of the membrane GluR2 subunit in the NAc. Intracerebroventricular administration of prazosin 30min before LPS injection abrogated the LPS-induced depressive-like behaviors. In opposition, administration of propranolol, a β-adrenoceptor antagonist, did not affect the LPS-induced downregulation of GluR1, the upregulation of GluR2, or the depressive-like behavior. CONCLUSIONS: These results suggest that LPS-activated α(1)-adrenoceptor-induced downregulation of membrane GluR1 in the mPFC and VTA is associated with inflammation-induced depressive-like behavior. Oxford University Press 2014-12-19 /pmc/articles/PMC4368860/ /pubmed/25539502 http://dx.doi.org/10.1093/ijnp/pyu005 Text en © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Sekio, Miyu
Seki, Kenjiro
Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title_full Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title_fullStr Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title_full_unstemmed Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title_short Lipopolysaccharide-Induced Depressive-Like Behavior is Associated with α(1)-Adrenoceptor Dependent Downregulation of the Membrane GluR1 Subunit in the Mouse Medial Prefrontal Cortex and Ventral Tegmental Area
title_sort lipopolysaccharide-induced depressive-like behavior is associated with α(1)-adrenoceptor dependent downregulation of the membrane glur1 subunit in the mouse medial prefrontal cortex and ventral tegmental area
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368860/
https://www.ncbi.nlm.nih.gov/pubmed/25539502
http://dx.doi.org/10.1093/ijnp/pyu005
work_keys_str_mv AT sekiomiyu lipopolysaccharideinduceddepressivelikebehaviorisassociatedwitha1adrenoceptordependentdownregulationofthemembraneglur1subunitinthemousemedialprefrontalcortexandventraltegmentalarea
AT sekikenjiro lipopolysaccharideinduceddepressivelikebehaviorisassociatedwitha1adrenoceptordependentdownregulationofthemembraneglur1subunitinthemousemedialprefrontalcortexandventraltegmentalarea