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Impact of anger emotional stress before pregnancy on adult male offspring

Previous studies have reported that maternal chronic stress or depression is linked to an increased risk of affective disorders in progeny. However, the impact of maternal chronic stress before pregnancy on the progeny of animal models is unknown. We investigated the behaviors and the neurobiology o...

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Autores principales: Wei, Sheng, Xiao, Xinyang, Wang, Jieqiong, Sun, Shiguang, Li, Zifa, Xu, Kaiyong, Li, Fang, Gao, Jie, Zhu, Dehao, Qiao, Mingqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716771/
https://www.ncbi.nlm.nih.gov/pubmed/29228731
http://dx.doi.org/10.18632/oncotarget.22007
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author Wei, Sheng
Xiao, Xinyang
Wang, Jieqiong
Sun, Shiguang
Li, Zifa
Xu, Kaiyong
Li, Fang
Gao, Jie
Zhu, Dehao
Qiao, Mingqi
author_facet Wei, Sheng
Xiao, Xinyang
Wang, Jieqiong
Sun, Shiguang
Li, Zifa
Xu, Kaiyong
Li, Fang
Gao, Jie
Zhu, Dehao
Qiao, Mingqi
author_sort Wei, Sheng
collection PubMed
description Previous studies have reported that maternal chronic stress or depression is linked to an increased risk of affective disorders in progeny. However, the impact of maternal chronic stress before pregnancy on the progeny of animal models is unknown. We investigated the behaviors and the neurobiology of 60-day-old male offspring of female rats subjected to 21 days of resident-intruder stress before pregnancy. An anger stressed parental rat model was established using the resident-intruder paradigm and it was evaluated using behavioral tests. Anger stressed maternal rats showed a significant increase in locomotion and aggression but a reduction in sucrose preference. Offspring subjected to pre-gestational anger stress displayed enhanced aggressive behaviors, reduced anxiety, and sucrose preference. Further, offspring subjected to pre-gestational stress showed significant impairments in the recognition index (RI) on the object recognition test and the number of platform crossings in the Morris water maze test. The monoaminergic system was significantly altered in pre-gestationally stressed offspring, and the expression of phosphorylated cyclic adenosine monophosphate response element binding protein (P-CREB), brain-derived neurotrophic factor (BDNF), and serotonin transporter (SERT) levels in pre-gestational stressed offspring were altered in some brain regions. Fluoxetine was used to treat pre-gestational stressed maternal rats and it significantly reduced the changes caused by stress, as evidenced by both behaviors and neural biochemical indexes in the offspring in some but not all cases. These findings suggest that anger stress before pregnancy could induce aggressive behaviors, cognitive deficits, and neurobiological alterations in offspring.
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spelling pubmed-57167712017-12-08 Impact of anger emotional stress before pregnancy on adult male offspring Wei, Sheng Xiao, Xinyang Wang, Jieqiong Sun, Shiguang Li, Zifa Xu, Kaiyong Li, Fang Gao, Jie Zhu, Dehao Qiao, Mingqi Oncotarget Research Paper Previous studies have reported that maternal chronic stress or depression is linked to an increased risk of affective disorders in progeny. However, the impact of maternal chronic stress before pregnancy on the progeny of animal models is unknown. We investigated the behaviors and the neurobiology of 60-day-old male offspring of female rats subjected to 21 days of resident-intruder stress before pregnancy. An anger stressed parental rat model was established using the resident-intruder paradigm and it was evaluated using behavioral tests. Anger stressed maternal rats showed a significant increase in locomotion and aggression but a reduction in sucrose preference. Offspring subjected to pre-gestational anger stress displayed enhanced aggressive behaviors, reduced anxiety, and sucrose preference. Further, offspring subjected to pre-gestational stress showed significant impairments in the recognition index (RI) on the object recognition test and the number of platform crossings in the Morris water maze test. The monoaminergic system was significantly altered in pre-gestationally stressed offspring, and the expression of phosphorylated cyclic adenosine monophosphate response element binding protein (P-CREB), brain-derived neurotrophic factor (BDNF), and serotonin transporter (SERT) levels in pre-gestational stressed offspring were altered in some brain regions. Fluoxetine was used to treat pre-gestational stressed maternal rats and it significantly reduced the changes caused by stress, as evidenced by both behaviors and neural biochemical indexes in the offspring in some but not all cases. These findings suggest that anger stress before pregnancy could induce aggressive behaviors, cognitive deficits, and neurobiological alterations in offspring. Impact Journals LLC 2017-10-24 /pmc/articles/PMC5716771/ /pubmed/29228731 http://dx.doi.org/10.18632/oncotarget.22007 Text en Copyright: © 2017 Wei et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Wei, Sheng
Xiao, Xinyang
Wang, Jieqiong
Sun, Shiguang
Li, Zifa
Xu, Kaiyong
Li, Fang
Gao, Jie
Zhu, Dehao
Qiao, Mingqi
Impact of anger emotional stress before pregnancy on adult male offspring
title Impact of anger emotional stress before pregnancy on adult male offspring
title_full Impact of anger emotional stress before pregnancy on adult male offspring
title_fullStr Impact of anger emotional stress before pregnancy on adult male offspring
title_full_unstemmed Impact of anger emotional stress before pregnancy on adult male offspring
title_short Impact of anger emotional stress before pregnancy on adult male offspring
title_sort impact of anger emotional stress before pregnancy on adult male offspring
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716771/
https://www.ncbi.nlm.nih.gov/pubmed/29228731
http://dx.doi.org/10.18632/oncotarget.22007
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