Brain Circuitry for Arousal from Apnea.

Clifford B Saper, Satvinder Kaur
{"title":"Brain Circuitry for Arousal from Apnea.","authors":"Clifford B Saper,&nbsp;Satvinder Kaur","doi":"10.1101/sqb.2018.83.038125","DOIUrl":null,"url":null,"abstract":"<p><p>We wanted to understand the brain circuitry that awakens the individual when there is elevated CO<sub>2</sub> or low O<sub>2</sub> (e.g., during sleep apnea or asphyxia). The sensory signals for high CO<sub>2</sub> and low O<sub>2</sub> all converge on the parabrachial nucleus (PB) of the pons, which contains neurons that project to the forebrain. So, we first deleted the vesicular glutamate transporter 2, necessary to load glutamate into synaptic vesicles, from neurons in the PB, and showed that this prevents awakening to high CO<sub>2</sub> or low O<sub>2</sub> We then showed that PB neurons that express calcitonin gene-related peptide (CGRP) show cFos staining during high CO<sub>2</sub> Using CGRP-Cre-ER mice, we expressed the inhibitory opsin archaerhodopsin just in the PB<sup>CGRP</sup> neurons. Photoinhibition of the PB<sup>CGRP</sup> neurons effectively prevented awakening to high CO<sub>2</sub>, as did photoinhibition of their terminals in the basal forebrain, amygdala, and lateral hypothalamus. The PB<sup>CGRP</sup> neurons are a key mediator of the wakening response to apnea.</p>","PeriodicalId":72635,"journal":{"name":"Cold Spring Harbor symposia on quantitative biology","volume":"83 ","pages":"63-69"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1101/sqb.2018.83.038125","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor symposia on quantitative biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/sqb.2018.83.038125","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/4/23 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

We wanted to understand the brain circuitry that awakens the individual when there is elevated CO2 or low O2 (e.g., during sleep apnea or asphyxia). The sensory signals for high CO2 and low O2 all converge on the parabrachial nucleus (PB) of the pons, which contains neurons that project to the forebrain. So, we first deleted the vesicular glutamate transporter 2, necessary to load glutamate into synaptic vesicles, from neurons in the PB, and showed that this prevents awakening to high CO2 or low O2 We then showed that PB neurons that express calcitonin gene-related peptide (CGRP) show cFos staining during high CO2 Using CGRP-Cre-ER mice, we expressed the inhibitory opsin archaerhodopsin just in the PBCGRP neurons. Photoinhibition of the PBCGRP neurons effectively prevented awakening to high CO2, as did photoinhibition of their terminals in the basal forebrain, amygdala, and lateral hypothalamus. The PBCGRP neurons are a key mediator of the wakening response to apnea.

从呼吸暂停唤醒的大脑回路。
我们想了解当二氧化碳浓度升高或氧气浓度降低时(例如,在睡眠呼吸暂停或窒息期间)唤醒个体的大脑回路。高二氧化碳和低氧气的感觉信号都汇聚在桥脑桥的臂旁核(PB)上,其中包含投射到前脑的神经元。因此,我们首先从PB神经元中删除了将谷氨酸装载到突触囊泡中所必需的囊泡性谷氨酸转运蛋白2,并发现这可以防止对高CO2或低O2的觉醒。然后,我们发现表达降钙素基因相关肽(CGRP)的PB神经元在高CO2时显示cFos染色。使用CGRP- cre - er小鼠,我们仅在PBCGRP神经元中表达抑制性视蛋白古紫质。PBCGRP神经元的光抑制有效地阻止了对高二氧化碳的觉醒,它们在基底前脑、杏仁核和外侧下丘脑的终端的光抑制也是如此。PBCGRP神经元是呼吸暂停唤醒反应的关键介质。
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
自引率
0.00%
发文量
0
×
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