The pre-Bötzinger complex is necessary for the expression of inspiratory and post-inspiratory motor discharge of the vagus

IF 1.9 4区 医学 Q3 PHYSIOLOGY Respiratory Physiology & Neurobiology Pub Date : 2023-12-02 DOI:10.1016/j.resp.2023.104202
Rishi R. Dhingra , Werner I. Furuya , Yi Kee Yoong , Mathias Dutschmann
{"title":"The pre-Bötzinger complex is necessary for the expression of inspiratory and post-inspiratory motor discharge of the vagus","authors":"Rishi R. Dhingra ,&nbsp;Werner I. Furuya ,&nbsp;Yi Kee Yoong ,&nbsp;Mathias Dutschmann","doi":"10.1016/j.resp.2023.104202","DOIUrl":null,"url":null,"abstract":"<div><p><span>The mammalian three-phase respiratory motor pattern of inspiration, post-inspiration and expiration is expressed in spinal and cranial motor nerve discharge and is generated by a distributed ponto-medullary respiratory pattern<span> generating network. Respiratory motor pattern generation depends on a rhythmogenic kernel located within the pre-Bötzinger complex (pre-BötC). In the present study, we tested the effect of unilateral and bilateral inactivation of the pre-BötC after local microinjection of the GABA</span></span><sub>A</sub><span><span> receptor agonist isoguvacine<span> (10 mM, 50 nl) on phrenic (PNA), hypoglossal (HNA) and vagal nerve (VNA) respiratory motor activities in an in situ perfused brainstem preparation of rats. Bilateral inactivation of the pre-BötC triggered cessation of phrenic (PNA), hypoglossal (HNA) and vagal (VNA) </span></span>nerve activities<span> for 15–20 min. Ipsilateral isoguvacine injections into the pre-BötC triggered transient (6–8 min) cessation of inspiratory and post-inspiratory VNA (p &lt; 0.001) and suppressed inspiratory HNA by − 70 ± 15% (p &lt; 0.01), while inspiratory PNA burst frequency increased by 46 ± 30% (p &lt; 0.01). Taken together, these observations confirm the role of the pre-BötC as the rhythmogenic kernel of the mammalian respiratory network in situ and highlight a significant role for the pre-BötC in the transmission of vagal inspiratory and post-inspiratory pre-motor drive to the nucleus ambiguus.</span></span></p></div>","PeriodicalId":20961,"journal":{"name":"Respiratory Physiology & Neurobiology","volume":"320 ","pages":"Article 104202"},"PeriodicalIF":1.9000,"publicationDate":"2023-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Respiratory Physiology & Neurobiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1569904823001908","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The mammalian three-phase respiratory motor pattern of inspiration, post-inspiration and expiration is expressed in spinal and cranial motor nerve discharge and is generated by a distributed ponto-medullary respiratory pattern generating network. Respiratory motor pattern generation depends on a rhythmogenic kernel located within the pre-Bötzinger complex (pre-BötC). In the present study, we tested the effect of unilateral and bilateral inactivation of the pre-BötC after local microinjection of the GABAA receptor agonist isoguvacine (10 mM, 50 nl) on phrenic (PNA), hypoglossal (HNA) and vagal nerve (VNA) respiratory motor activities in an in situ perfused brainstem preparation of rats. Bilateral inactivation of the pre-BötC triggered cessation of phrenic (PNA), hypoglossal (HNA) and vagal (VNA) nerve activities for 15–20 min. Ipsilateral isoguvacine injections into the pre-BötC triggered transient (6–8 min) cessation of inspiratory and post-inspiratory VNA (p < 0.001) and suppressed inspiratory HNA by − 70 ± 15% (p < 0.01), while inspiratory PNA burst frequency increased by 46 ± 30% (p < 0.01). Taken together, these observations confirm the role of the pre-BötC as the rhythmogenic kernel of the mammalian respiratory network in situ and highlight a significant role for the pre-BötC in the transmission of vagal inspiratory and post-inspiratory pre-motor drive to the nucleus ambiguus.

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
pre-Bötzinger复合体对于迷走神经的吸气和吸气后运动放电的表达是必需的。
哺乳动物吸气、吸气后和呼气的三相呼吸运动模式以脊髓和颅运动神经放电的形式表达,由分布的桥髓呼吸模式生成网络产生。呼吸运动模式的产生依赖于位于pre-Bötzinger复合体内的节律性核(pre-BötC)。在本研究中,我们测试了局部微量注射GABAA受体激动剂异guvacine (10mM, 50nl)后对大鼠原位灌注脑干制剂中膈神经(PNA)、舌下神经(HNA)和迷走神经(VNA)呼吸运动活动的影响。双侧pre-BötC失活触发膈神经(PNA)、舌下神经(HNA)和迷走神经(VNA)活动停止15-20min。同侧异古瓦卡因注射pre-BötC触发吸气和吸气后VNA短暂(6-8min)停止(p
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
CiteScore
4.80
自引率
8.70%
发文量
104
审稿时长
54 days
期刊介绍: Respiratory Physiology & Neurobiology (RESPNB) publishes original articles and invited reviews concerning physiology and pathophysiology of respiration in its broadest sense. Although a special focus is on topics in neurobiology, high quality papers in respiratory molecular and cellular biology are also welcome, as are high-quality papers in traditional areas, such as: -Mechanics of breathing- Gas exchange and acid-base balance- Respiration at rest and exercise- Respiration in unusual conditions, like high or low pressure or changes of temperature, low ambient oxygen- Embryonic and adult respiration- Comparative respiratory physiology. Papers on clinical aspects, original methods, as well as theoretical papers are also considered as long as they foster the understanding of respiratory physiology and pathophysiology.
期刊最新文献
TRPA1 contributes to respiratory depression from tobacco aerosol. THE ACUTE EFFECT OF BILATERAL CATHODIC TRANSCRANIAL DIRECT CURRENT STIMULATION ON RESPIRATORY MUSCLE STRENGTH AND ENDURANCE. Glycolytic metabolism modulation on spinal neuroinflammation and vital functions following cervical spinal cord injury. Impact of microbial diversity on inflammatory cytokines and respiratory pattern measured in whole-body plethysmography in guinea pig models. Editorial Board
×
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