Literature DB >> 35507233

The Combined Effects of Perinatal Ethanol and Early-Life Stress on Cognition and Risk-Taking Behavior through Oxidative Stress in Rats.

Farzaneh Bagheri1, Iran Goudarzi2, Taghi Lashkarbolouki1, Mahmoud Elahdadi Salmani1, Afsaneh Goudarzi3, Sara Morley-Fletcher4.   

Abstract

Both prenatal ethanol and early-life stress have been shown to induce reduced risk-taking and explorative behavior as well as cognitive dysfunction in the offspring. In this study, we examined the effect of combined exposure to ethanol and early stress on maternal care, exploratory behavior, memory performances, and oxidative stress in male offspring. Pregnant rats were exposed to ethanol (4 g/kg) from gestational day (GD) 6-to postnatal day (PND) 14 and limited nesting material (LNS) from PND0-PND14 individually or in combination. Maternal behavior was evaluated during diurnal cycle. The level of corticosterone hormone and markers of oxidative stress were evaluated in the pups. Risk-taking and explorative behavior were assessed with the elevated-plus maze (EPM) test and cognitive behavior with the Morris water maze (MWM), novel object recognition (NORT), and object location memory (OLM) tests. In the mothers, perinatal alcohol or LNS either alone or in combination decreased maternal behavior. In the offspring, the combination of the two factors significantly increased the pup's plasma corticosterone concentration in comparison with ethanol and LNS alone. Reduced risk-taking behavior was observed in the ethanol, LNS and ethanol + LNS groups compared with the control group, and this was amplified in the co-exposure of ethanol and LNS groups. The MWM, NORT, and OLM tests revealed spatial and recognition memory impairment in the ethanol and LNS groups. This impairment was more profound in the co-exposure of ethanol and LNS. Also, we observed a significant decrease in superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities and an increase in malondialdehyde (MDA) level in the hippocampus of ethanol and LNS co-exposed animals as compared with individual exposure of ethanol and LNS. While each factor independently produced similar outcomes, the results indicate that the dual exposure paradigm could significantly strengthen the outcomes.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Keywords:  Anxiety; Early-life stress; Ethanol; Learning and memory; Oxidative stress; Rat offspring

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Year:  2022        PMID: 35507233     DOI: 10.1007/s12640-022-00506-6

Source DB:  PubMed          Journal:  Neurotox Res        ISSN: 1029-8428            Impact factor:   3.978


  34 in total

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4.  Protection against oxidative stress-induced neuronal cell death--a novel role for RU486.

Authors:  C Behl; T Trapp; T Skutella; F Holsboer
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5.  Melatonin prevents oxidative damage induced by maternal ethanol administration and reduces homocysteine in the cerebellum of rat pups.

Authors:  Farzaneh Bagheri; Iran Goudarzi; Taghi Lashkarbolouki; Mahmoud Elahdadi Salmani
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8.  Repeated restraint stress induces oxidative damage in rat hippocampus.

Authors:  Fernanda U Fontella; Ionara R Siqueira; Ana Paula S Vasconcellos; Angela S Tabajara; Carlos A Netto; Carla Dalmaz
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9.  Imbalanced synaptic plasticity induced spatial cognition impairment in male offspring rats treated with chronic prenatal ethanol exposure.

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Journal:  Alcohol Clin Exp Res       Date:  2012-12-14       Impact factor: 3.455

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Journal:  Front Cell Neurosci       Date:  2022-08-22       Impact factor: 6.147

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