Sex-Specific Effects of Stress on Mood-Related Gene Expression

K. Barko, W. Paden, Kelly M. Cahill, M. Seney, R. Logan
{"title":"Sex-Specific Effects of Stress on Mood-Related Gene Expression","authors":"K. Barko, W. Paden, Kelly M. Cahill, M. Seney, R. Logan","doi":"10.1159/000499105","DOIUrl":null,"url":null,"abstract":"Women are twice as likely as men to be diagnosed with major depressive disorder (MDD). Recent studies report distinct molecular changes in depressed men and women across mesocorticolimbic brain regions. However, it is unclear which sex-related factors drive distinct MDD-associated pathology. The goal of this study was to use mouse experimental systems to investigate sex-specific mechanisms underlying the distinct molecular profiles of MDD in men and women. We used unpredictable chronic mild stress to induce an elevated anxiety-/depressive-like state and “four core genotypes” (FCG) mice to probe for sex-specific mechanisms. As predicted, based on previous implications in mood, stress impacted the expression of several dopamine-, GABA-, and glutamate-related genes. Some of these effects, specifically in the prefrontal cortex, were genetic sex-specific, with effects in XX mice but not in XY mice. Stress also impacted gene expression differently across the mesocorticolimbic circuit, with increased expression of mood-related genes in the prefrontal cortex and nucleus accumbens, but decreased expression in basolateral amygdala. Our results suggest that females are sensitive to the effects of chronic stress, partly due to their genetic sex, independent of gonadal hormones. Furthermore, these results point to the prefrontal cortex as the node in the mesocorticolimbic circuitry with the strongest female-specific effects.","PeriodicalId":18957,"journal":{"name":"Molecular Neuropsychiatry","volume":"45 1","pages":"162 - 176"},"PeriodicalIF":0.0000,"publicationDate":"2019-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"27","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Neuropsychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000499105","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 27

Abstract

Women are twice as likely as men to be diagnosed with major depressive disorder (MDD). Recent studies report distinct molecular changes in depressed men and women across mesocorticolimbic brain regions. However, it is unclear which sex-related factors drive distinct MDD-associated pathology. The goal of this study was to use mouse experimental systems to investigate sex-specific mechanisms underlying the distinct molecular profiles of MDD in men and women. We used unpredictable chronic mild stress to induce an elevated anxiety-/depressive-like state and “four core genotypes” (FCG) mice to probe for sex-specific mechanisms. As predicted, based on previous implications in mood, stress impacted the expression of several dopamine-, GABA-, and glutamate-related genes. Some of these effects, specifically in the prefrontal cortex, were genetic sex-specific, with effects in XX mice but not in XY mice. Stress also impacted gene expression differently across the mesocorticolimbic circuit, with increased expression of mood-related genes in the prefrontal cortex and nucleus accumbens, but decreased expression in basolateral amygdala. Our results suggest that females are sensitive to the effects of chronic stress, partly due to their genetic sex, independent of gonadal hormones. Furthermore, these results point to the prefrontal cortex as the node in the mesocorticolimbic circuitry with the strongest female-specific effects.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
应激对情绪相关基因表达的性别特异性影响
女性被诊断为重度抑郁症(MDD)的可能性是男性的两倍。最近的研究报告了抑郁症男性和女性中皮质边缘脑区的明显分子变化。然而,目前尚不清楚哪些性别相关因素驱动不同的mdd相关病理。本研究的目的是利用小鼠实验系统来研究男性和女性重度抑郁症不同分子特征背后的性别特异性机制。我们使用不可预测的慢性轻度应激诱导焦虑/抑郁样状态升高,并使用“四核心基因型”(FCG)小鼠来探索性别特异性机制。正如预测的那样,基于先前对情绪的影响,压力影响了几种多巴胺,GABA和谷氨酸相关基因的表达。其中一些影响,特别是在前额叶皮层,是遗传性别特异性的,在XX小鼠中有影响,而在XY小鼠中没有。应激对中皮质边缘回路基因表达的影响也不同,前额叶皮层和伏隔核的情绪相关基因表达增加,而杏仁核基底外侧的表达减少。我们的研究结果表明,女性对慢性压力的影响很敏感,部分原因是由于她们的遗传性别,与性腺激素无关。此外,这些结果表明前额叶皮层是中皮质边缘回路的节点,对女性的特异性影响最大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Genome-Wide Association Study of Sleep Disturbances in Depressive Disorders. EAAT2 as a Research Target in Bipolar Disorder and Unipolar Depression: A Systematic Review. The Role of PTEN in Neurodevelopment. Using Chronobiological Phenotypes to Address Heterogeneity in Bipolar Disorder. The Genetic Relevance of Human Induced Pluripotent Stem Cell-Derived Microglia to Alzheimer's Disease and Major Neuropsychiatric Disorders.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1