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


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
22 04 2020
Historique:
received: 26 03 2020
revised: 16 04 2020
accepted: 19 04 2020
entrez: 26 4 2020
pubmed: 26 4 2020
medline: 20 2 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32331397
pii: cells9041048
doi: 10.3390/cells9041048
pmc: PMC7226255
pii:
doi:

Substances chimiques

Vascular Endothelial Growth Factor A 0
Extracellular Signal-Regulated MAP Kinases EC 2.7.11.24

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Austrian Science Fund FWF
ID : P 27520
Pays : Austria

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Auteurs

Spyridon Sideromenos (S)

Department of Neurophysiology and Neuropharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Claudia Lindtner (C)

Department of Paediatrics, Division of Neonatology, Pediatric Intensive Care Medicine and Neuropaediatrics, Medical University of Vienna, 1090 Vienna, Austria.

Alice Zambon (A)

Department of Neurophysiology and Neuropharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Orsolya Horvath (O)

Department of Neurophysiology and Neuropharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Angelika Berger (A)

Department of Paediatrics, Division of Neonatology, Pediatric Intensive Care Medicine and Neuropaediatrics, Medical University of Vienna, 1090 Vienna, Austria.

Daniela D Pollak (DD)

Department of Neurophysiology and Neuropharmacology, Medical University of Vienna, 1090 Vienna, Austria.

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Classifications MeSH