GABAergic neurons in central amygdala contribute to orchestrating anxiety-like behaviors and breathing patterns

IF 14.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Xiaoyi Wang, Shangyu Bi, Ziteng Yue, Xinxin Chen, Yuhang Liu, Tianjiao Deng, Liuqi Shao, Xinyi Jing, Cuidie Wang, Yakun Wang, Wei He, Hongxiao Yu, Luo Shi, Fang Yuan, Sheng Wang
{"title":"GABAergic neurons in central amygdala contribute to orchestrating anxiety-like behaviors and breathing patterns","authors":"Xiaoyi Wang, Shangyu Bi, Ziteng Yue, Xinxin Chen, Yuhang Liu, Tianjiao Deng, Liuqi Shao, Xinyi Jing, Cuidie Wang, Yakun Wang, Wei He, Hongxiao Yu, Luo Shi, Fang Yuan, Sheng Wang","doi":"10.1038/s41467-025-58791-6","DOIUrl":null,"url":null,"abstract":"<p>Anxiety is characterized by dysregulated respiratory reactivity to emotional stimuli. The central amygdala (CeA) is a pivotal structure involved in processing emotional alterations, but its involvement in orchestrating anxiety-like behaviors and specific breathing patterns remains largely unexplored. Our findings demonstrate that the acute restraint stress (ARS) induces anxiety-like behaviors in mice, marked by prolonged grooming time and faster respiratory frequency (RF). Conversely, silencing GABAergic CeA neurons reduces post-ARS anxiety-like behaviors, as well as the associated increases in grooming time and RF. In actively behaving mice, stimulation of GABAergic CeA neurons elicits anxiety-like behaviors, concurrently prolongs grooming time, accelerates RF through a CeA-thalamic paraventricular nucleus (PVT) circuit. In either behaviorally quiescent or anesthetized mice, stimulation of these neurons significantly increases RF but does not induce anxiety-like behaviors through the CeA-lateral parabrachial nucleus (LPBN) circuit. Collectively, GABAergic CeA neurons are instrumental in orchestrating anxiety-like behaviors and breathing patterns primarily through the CeA-PVT and CeA-LPBN circuits, respectively.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"40 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-58791-6","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Anxiety is characterized by dysregulated respiratory reactivity to emotional stimuli. The central amygdala (CeA) is a pivotal structure involved in processing emotional alterations, but its involvement in orchestrating anxiety-like behaviors and specific breathing patterns remains largely unexplored. Our findings demonstrate that the acute restraint stress (ARS) induces anxiety-like behaviors in mice, marked by prolonged grooming time and faster respiratory frequency (RF). Conversely, silencing GABAergic CeA neurons reduces post-ARS anxiety-like behaviors, as well as the associated increases in grooming time and RF. In actively behaving mice, stimulation of GABAergic CeA neurons elicits anxiety-like behaviors, concurrently prolongs grooming time, accelerates RF through a CeA-thalamic paraventricular nucleus (PVT) circuit. In either behaviorally quiescent or anesthetized mice, stimulation of these neurons significantly increases RF but does not induce anxiety-like behaviors through the CeA-lateral parabrachial nucleus (LPBN) circuit. Collectively, GABAergic CeA neurons are instrumental in orchestrating anxiety-like behaviors and breathing patterns primarily through the CeA-PVT and CeA-LPBN circuits, respectively.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信