Abstract

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.

Highlights

  • Depression is a highly debilitating disorder which affects more than 260 million people worldwide [1]

  • We report that vascular endothelial growth factor (VEGF) ameliorated the behavioral deficits present in the tail suspension test (TST) but had no effect in the sucrose preference test (SPT)

  • VEGF or vehicle solution directly to the lateral ventricles of the brain at a dose of 30 ng/day for a period of one week. This resulted in a 2 × 2 design with four experimental groups: Control offspring receiving vehicle (CON:VEH) or VEGF solution (CON:VEGF) and maternal immune activation (MIA) offspring receiving vehicle (MIA:VEH)

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Summary

Introduction

Depression is a highly debilitating disorder which affects more than 260 million people worldwide [1]. The fetal period represents an extremely critical stage for the developing brain and different stressors [3], such as activation of the maternal immune system, can impede normal brain development [4,5]. Cells 2020, 9, 1048 been postulated that maternal infections predispose offspring to certain neuropsychiatric disorders, including depression, schizophrenia and autism spectrum disorders [6]. This association was first established by epidemiological studies in the human population [7,8] and recapitulated and extended in various animal models

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