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VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation

Maternal immune activation (MIA) during pregnancy impacts offspring neurodevelopmental trajectories and induces lifelong consequences, including emotional and cognitive alterations. Using the polyinosinic:polycytidilic acid (PIC) MIA model we have previously demonstrated enhanced depression-like beh...

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Autores principales: Sideromenos, Spyridon, Lindtner, Claudia, Zambon, Alice, Horvath, Orsolya, Berger, Angelika, Pollak, Daniela D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226255/
https://www.ncbi.nlm.nih.gov/pubmed/32331397
http://dx.doi.org/10.3390/cells9041048
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author Sideromenos, Spyridon
Lindtner, Claudia
Zambon, Alice
Horvath, Orsolya
Berger, Angelika
Pollak, Daniela D.
author_facet Sideromenos, Spyridon
Lindtner, Claudia
Zambon, Alice
Horvath, Orsolya
Berger, Angelika
Pollak, Daniela D.
author_sort Sideromenos, Spyridon
collection PubMed
description Maternal immune activation (MIA) during pregnancy impacts offspring neurodevelopmental trajectories and induces lifelong consequences, including emotional and cognitive alterations. Using the polyinosinic:polycytidilic acid (PIC) MIA model we have previously demonstrated enhanced depression-like behavior in adult MIA offspring, which was associated with reduced expression of the vascular endothelial growth factor (VEGF) receptor 2 (VEGFR2) in the hippocampus. Since VEGF mediates the effects of various antidepressant agents, we here set out to explore whether VEGF administration could rescue the depression-like behavioral deficits in MIA offspring. To test our hypothesis, control and MIA offspring were intracerebroventricularly (i.c.v.) infused with either VEGF or vehicle solution and depression-related behavior was assessed in the sucrose preference test (SPT) and the tail suspension test (TST). As a surrogate of VEGF activity, the phosphorylation of the extracellular signal-regulated kinase (ERK) in hippocampus was quantified. We found that VEGF treatment reduced depression-related behavioral despair in the TST in MIA offspring but had no effect on anhedonia-like behavior in the SPT. While VEGF administration induced the phosphorylation of ERK in the hippocampus of control offspring, this effect was blunted in the MIA offspring. We conclude that VEGF administration, at the dosage tested, beneficially affects some aspects of the depression-like phenotype in the adult MIA offspring, inviting further studies using different dosage regimes to further explore the therapeutic potential of VEGF treatment in MIA-related changes in brain function and behavior.
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spelling pubmed-72262552020-05-18 VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation Sideromenos, Spyridon Lindtner, Claudia Zambon, Alice Horvath, Orsolya Berger, Angelika Pollak, Daniela D. Cells Communication Maternal immune activation (MIA) during pregnancy impacts offspring neurodevelopmental trajectories and induces lifelong consequences, including emotional and cognitive alterations. Using the polyinosinic:polycytidilic acid (PIC) MIA model we have previously demonstrated enhanced depression-like behavior in adult MIA offspring, which was associated with reduced expression of the vascular endothelial growth factor (VEGF) receptor 2 (VEGFR2) in the hippocampus. Since VEGF mediates the effects of various antidepressant agents, we here set out to explore whether VEGF administration could rescue the depression-like behavioral deficits in MIA offspring. To test our hypothesis, control and MIA offspring were intracerebroventricularly (i.c.v.) infused with either VEGF or vehicle solution and depression-related behavior was assessed in the sucrose preference test (SPT) and the tail suspension test (TST). As a surrogate of VEGF activity, the phosphorylation of the extracellular signal-regulated kinase (ERK) in hippocampus was quantified. We found that VEGF treatment reduced depression-related behavioral despair in the TST in MIA offspring but had no effect on anhedonia-like behavior in the SPT. While VEGF administration induced the phosphorylation of ERK in the hippocampus of control offspring, this effect was blunted in the MIA offspring. We conclude that VEGF administration, at the dosage tested, beneficially affects some aspects of the depression-like phenotype in the adult MIA offspring, inviting further studies using different dosage regimes to further explore the therapeutic potential of VEGF treatment in MIA-related changes in brain function and behavior. MDPI 2020-04-22 /pmc/articles/PMC7226255/ /pubmed/32331397 http://dx.doi.org/10.3390/cells9041048 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Sideromenos, Spyridon
Lindtner, Claudia
Zambon, Alice
Horvath, Orsolya
Berger, Angelika
Pollak, Daniela D.
VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title_full VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title_fullStr VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title_full_unstemmed VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title_short VEGF Treatment Ameliorates Depression-Like Behavior in Adult Offspring after Maternal Immune Activation
title_sort vegf treatment ameliorates depression-like behavior in adult offspring after maternal immune activation
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226255/
https://www.ncbi.nlm.nih.gov/pubmed/32331397
http://dx.doi.org/10.3390/cells9041048
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