Separate anterior paraventricular thalamus projections differentially regulate sensory and affective aspects of pain.

IF 7.5 1区 生物学 Q1 CELL BIOLOGY
Selomon Assefa Mindaye, Wei-Hsin Chen, Shih-Che Lin, Yong-Cyuan Chen, Mohamed Abbas Abdelaziz, Yi-Shiuan Tzeng, Arthur Chun-Chieh Shih, Shih-Yu Chen, Shi-Bing Yang, Chien-Chang Chen
{"title":"Separate anterior paraventricular thalamus projections differentially regulate sensory and affective aspects of pain.","authors":"Selomon Assefa Mindaye, Wei-Hsin Chen, Shih-Che Lin, Yong-Cyuan Chen, Mohamed Abbas Abdelaziz, Yi-Shiuan Tzeng, Arthur Chun-Chieh Shih, Shih-Yu Chen, Shi-Bing Yang, Chien-Chang Chen","doi":"10.1016/j.celrep.2024.114946","DOIUrl":null,"url":null,"abstract":"<p><p>The experience of pain is complex, involving both sensory and affective components, yet the underlying neural mechanisms remain elusive. Here, we show that formalin-induced pain behaviors coincide with increased responses in glutamatergic neurons within the anterior paraventricular nucleus of the thalamus (PVA). Furthermore, we describe non-overlapping subpopulations of PVAVgluT2 neurons involved in sensory and affective pain processing, whose activity varies across different pain states. Activating PVA glutamatergic neurons is sufficient to induce mechanical hypersensitivity and aversion behaviors, whereas suppression ameliorates formalin-induced pain. Furthermore, we identify the segregation of PVA<sup>VgluT2</sup> projections to the bed nucleus of the stria terminalis (BNST) and nucleus accumbens (NAc), each influencing specific aspects of pain-like behavior. This finding provides an important insight into the mechanism of distinct components of pain, highlighting the pivotal role of PVA in mediating different aspects of pain-like behavior with distinct circuits.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":"43 11","pages":"114946"},"PeriodicalIF":7.5000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.celrep.2024.114946","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The experience of pain is complex, involving both sensory and affective components, yet the underlying neural mechanisms remain elusive. Here, we show that formalin-induced pain behaviors coincide with increased responses in glutamatergic neurons within the anterior paraventricular nucleus of the thalamus (PVA). Furthermore, we describe non-overlapping subpopulations of PVAVgluT2 neurons involved in sensory and affective pain processing, whose activity varies across different pain states. Activating PVA glutamatergic neurons is sufficient to induce mechanical hypersensitivity and aversion behaviors, whereas suppression ameliorates formalin-induced pain. Furthermore, we identify the segregation of PVAVgluT2 projections to the bed nucleus of the stria terminalis (BNST) and nucleus accumbens (NAc), each influencing specific aspects of pain-like behavior. This finding provides an important insight into the mechanism of distinct components of pain, highlighting the pivotal role of PVA in mediating different aspects of pain-like behavior with distinct circuits.

独立的丘脑室旁前突起对疼痛的感觉和情感方面起着不同的调节作用。
疼痛的体验是复杂的,涉及感觉和情感两个部分,但其潜在的神经机制仍然难以捉摸。在这里,我们发现福尔马林诱导的疼痛行为与丘脑前室旁核(PVA)中谷氨酸能神经元反应的增加相吻合。此外,我们还描述了参与感觉和情感疼痛处理的 PVAVgluT2 神经元的非重叠亚群,它们的活动在不同的疼痛状态下有所不同。激活 PVA 谷氨酸能神经元足以诱导机械过敏和厌恶行为,而抑制则能改善福尔马林诱导的疼痛。此外,我们还发现了 PVAVgluT2 向纹状体末端床核(BNST)和阿氏核(NAc)的分离投射,它们分别影响疼痛样行为的特定方面。这一发现为了解疼痛不同组成部分的机制提供了一个重要的视角,突出了 PVA 在通过不同回路介导类似疼痛行为的不同方面所起的关键作用。
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 求助全文
来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
×
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