慢性间歇性缺氧会削弱舌下运动核的去甲肾上腺素能神经支配

IF 1.9 4区 医学 Q3 PHYSIOLOGY Respiratory Physiology & Neurobiology Pub Date : 2023-12-21 DOI:10.1016/j.resp.2023.104206
Rachael Herlihy , Leonardo Frasson Dos Reis , Anzor Gvritishvili , Maya Kvizhinadze , Elizabeth Dybas , Atul Malhotra , Victor B. Fenik , Irma Rukhadze
{"title":"慢性间歇性缺氧会削弱舌下运动核的去甲肾上腺素能神经支配","authors":"Rachael Herlihy ,&nbsp;Leonardo Frasson Dos Reis ,&nbsp;Anzor Gvritishvili ,&nbsp;Maya Kvizhinadze ,&nbsp;Elizabeth Dybas ,&nbsp;Atul Malhotra ,&nbsp;Victor B. Fenik ,&nbsp;Irma Rukhadze","doi":"10.1016/j.resp.2023.104206","DOIUrl":null,"url":null,"abstract":"<div><p><span>The state-dependent noradrenergic activation of hypoglossal motoneurons<span> plays an important role in the maintenance of upper airway patency<span><span> and pathophysiology of </span>obstructive sleep apnea<span> (OSA). Chronic intermittent hypoxia (CIH), a major pathogenic factor of OSA, contributes to the risk for developing </span></span></span></span>neurodegenerative disorders<span><span> in OSA patients. Using anterograde tracer, channelrhodopsin-2, we mapped axonal projections from noradrenergic A7 and SubCoeruleus neurons to </span>hypoglossal nucleus<span> in DBH-cre mice and assessed the effect of CIH on these projections. We found that CIH significantly reduced the number of axonal projections from SubCoeruleus neurons to both dorsal (by 68%) and to ventral (by73%) subregions of the hypoglossal motor nucleus compared to sham-treated animals. The animals’ body weight was also negatively affected by CIH. Both effects, the decrease in axonal projections and body weight, were more pronounced in male than female mice, which was likely caused by less sensitivity of female mice to CIH as compared to males. The A7 neurons appeared to have limited projections to the hypoglossal nucleus. Our findings suggest that CIH-induced reduction of noradrenergic innervation of hypoglossal motoneurons may exacerbate progression of OSA, especially in men.</span></span></p></div>","PeriodicalId":20961,"journal":{"name":"Respiratory Physiology & Neurobiology","volume":"321 ","pages":"Article 104206"},"PeriodicalIF":1.9000,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chronic intermittent hypoxia attenuates noradrenergic innervation of hypoglossal motor nucleus\",\"authors\":\"Rachael Herlihy ,&nbsp;Leonardo Frasson Dos Reis ,&nbsp;Anzor Gvritishvili ,&nbsp;Maya Kvizhinadze ,&nbsp;Elizabeth Dybas ,&nbsp;Atul Malhotra ,&nbsp;Victor B. Fenik ,&nbsp;Irma Rukhadze\",\"doi\":\"10.1016/j.resp.2023.104206\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>The state-dependent noradrenergic activation of hypoglossal motoneurons<span> plays an important role in the maintenance of upper airway patency<span><span> and pathophysiology of </span>obstructive sleep apnea<span> (OSA). Chronic intermittent hypoxia (CIH), a major pathogenic factor of OSA, contributes to the risk for developing </span></span></span></span>neurodegenerative disorders<span><span> in OSA patients. Using anterograde tracer, channelrhodopsin-2, we mapped axonal projections from noradrenergic A7 and SubCoeruleus neurons to </span>hypoglossal nucleus<span> in DBH-cre mice and assessed the effect of CIH on these projections. We found that CIH significantly reduced the number of axonal projections from SubCoeruleus neurons to both dorsal (by 68%) and to ventral (by73%) subregions of the hypoglossal motor nucleus compared to sham-treated animals. The animals’ body weight was also negatively affected by CIH. Both effects, the decrease in axonal projections and body weight, were more pronounced in male than female mice, which was likely caused by less sensitivity of female mice to CIH as compared to males. The A7 neurons appeared to have limited projections to the hypoglossal nucleus. Our findings suggest that CIH-induced reduction of noradrenergic innervation of hypoglossal motoneurons may exacerbate progression of OSA, especially in men.</span></span></p></div>\",\"PeriodicalId\":20961,\"journal\":{\"name\":\"Respiratory Physiology & Neurobiology\",\"volume\":\"321 \",\"pages\":\"Article 104206\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2023-12-21\",\"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/S1569904823001945\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Respiratory Physiology & Neurobiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1569904823001945","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

摘要

在维持上气道通畅和阻塞性睡眠呼吸暂停(OSA)的病理生理过程中,下舌运动神经元的状态依赖性去甲肾上腺素能激活起着重要作用。慢性间歇性缺氧(CIH)是 OSA 的主要致病因素,也是导致 OSA 患者罹患神经退行性疾病的风险因素之一。我们利用前向性示踪剂channelrhodopsin-2绘制了DBH-cre小鼠去甲肾上腺素能A7和小叶下神经元到舌下核的轴突投射图,并评估了CIH对这些投射的影响。我们发现,与假治疗动物相比,CIH 明显降低了从小叶下神经元向舌下运动核背侧(68%)和腹侧(73%)亚区的轴突投射数量。动物的体重也受到 CIH 的负面影响。雄性小鼠比雌性小鼠的轴突投射和体重下降更为明显,这可能是因为雌性小鼠对CIH的敏感性低于雄性小鼠。A7神经元对舌下核的投射似乎有限。我们的研究结果表明,CIH 引起的舌下运动神经元去甲肾上腺素能神经支配的减少可能会加剧 OSA 的恶化,尤其是对男性而言。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Chronic intermittent hypoxia attenuates noradrenergic innervation of hypoglossal motor nucleus

The state-dependent noradrenergic activation of hypoglossal motoneurons plays an important role in the maintenance of upper airway patency and pathophysiology of obstructive sleep apnea (OSA). Chronic intermittent hypoxia (CIH), a major pathogenic factor of OSA, contributes to the risk for developing neurodegenerative disorders in OSA patients. Using anterograde tracer, channelrhodopsin-2, we mapped axonal projections from noradrenergic A7 and SubCoeruleus neurons to hypoglossal nucleus in DBH-cre mice and assessed the effect of CIH on these projections. We found that CIH significantly reduced the number of axonal projections from SubCoeruleus neurons to both dorsal (by 68%) and to ventral (by73%) subregions of the hypoglossal motor nucleus compared to sham-treated animals. The animals’ body weight was also negatively affected by CIH. Both effects, the decrease in axonal projections and body weight, were more pronounced in male than female mice, which was likely caused by less sensitivity of female mice to CIH as compared to males. The A7 neurons appeared to have limited projections to the hypoglossal nucleus. Our findings suggest that CIH-induced reduction of noradrenergic innervation of hypoglossal motoneurons may exacerbate progression of OSA, especially in men.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 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