Literature DB >> 31228589

Sex-dependent effects of early unstable post-natal environment on response to positive and negative stimuli in adult mice.

Matteo Di Segni1, Diego Andolina1, Sebastian Luca D'Addario2, Lucy Babicola3, Donald Ielpo2, Alessandra Luchetti4, Tiziana Pascucci1, Luisa Lo Iacono1, Francesca R D'Amato5, Rossella Ventura6.   

Abstract

Alterations in early environmental conditions that interfere with the creation of a stable mother-pup bond have been suggested to be a risk factor for the development of stress-related psychopathologies later in life. The long-lasting effects of early experiences are mediated by changes in various cerebral circuits, such as the corticolimbic system, which processes aversive and rewarding stimuli. However, it is evident that the early environment is not sufficient per se to induce psychiatric disorders; interindividual (eg, sex-based) differences in the response to environmental challenges exist. To examine the sex-related effects that are induced by an early experience on later events in adulthood, we determine the enduring effects of repeated cross-fostering (RCF) in female and male C57BL/6J mice. To this end, we assessed the behavioral phenotype of RCF and control (male and female) mice in the saccharine preference test and cocaine-induced conditioned place preference to evaluate the response to natural and pharmacological stimuli and in the elevated plus maze test and forced swimming test to measure their anxiety- and depression-like behavior. We also evaluated FST-induced c-Fos immunoreactivity in various brain regions that are engaged in the response to acute stress exposure (FST). Notably, RCF has opposing effects on the adult response to these tests between sexes, directing male mice toward an "anhedonia-like" phenotype and increasing the sensitivity for rewarding stimuli in female mice.
Copyright © 2019 IBRO. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  anhedonia-like phenotype; mouse; sex-related differences; unstable early environment

Mesh:

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Year:  2019        PMID: 31228589     DOI: 10.1016/j.neuroscience.2019.06.016

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


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