{"title":"脑干阿片肽能神经元调节小鼠的咳嗽反射","authors":"Haicheng Lu, Guoqing Chen, Miao Zhao, Huating Gu, Wenxuan Zheng, Xiating Li, Meizhu Huang, Dandan Geng, Minhui Yu, Xuyan Guan, Li Zhang, Huimeng Song, Yaning Li, Menghua Wu, Fan Zhang, Dapeng Li, Qingfeng Wu, Congping Shang, Zhiyong Xie, Peng Cao","doi":"10.1016/j.xinn.2024.100721","DOIUrl":null,"url":null,"abstract":"<p><p>Cough is a vital defensive reflex for expelling harmful substances from the airway. The sensory afferents for the cough reflex have been intensively studied. However, the brain mechanisms underlying the cough reflex remain poorly understood. Here, we developed a paradigm to quantitatively measure cough-like reflexes in mice. Using this paradigm, we found that <i>prodynorphin</i>-expressing (<i>Pdyn</i>+) neurons in the nucleus of the solitary tract (NTS) are critical for capsaicin-induced cough-like reflexes. These neurons receive cough-related neural signals from <i>Trpv1</i>+ vagal sensory neurons. The activation of <i>Pdyn</i>+ NTS neurons triggered respiratory responses resembling cough-like reflexes. Among the divergent projections of <i>Pdyn</i>+ NTS neurons, a glutamatergic pathway projecting to the caudal ventral respiratory group (cVRG), the canonical cough center, was necessary and sufficient for capsaicin-induced cough-like reflexes. These results reveal that <i>Pdyn</i>+ NTS neurons, as a key neuronal population at the entry point of the vagus nerve to the brainstem, initiate cough-like reflexes in mice.</p>","PeriodicalId":36121,"journal":{"name":"The Innovation","volume":"5 6","pages":"100721"},"PeriodicalIF":33.2000,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11551472/pdf/","citationCount":"0","resultStr":"{\"title\":\"Brainstem opioid peptidergic neurons regulate cough reflexes in mice.\",\"authors\":\"Haicheng Lu, Guoqing Chen, Miao Zhao, Huating Gu, Wenxuan Zheng, Xiating Li, Meizhu Huang, Dandan Geng, Minhui Yu, Xuyan Guan, Li Zhang, Huimeng Song, Yaning Li, Menghua Wu, Fan Zhang, Dapeng Li, Qingfeng Wu, Congping Shang, Zhiyong Xie, Peng Cao\",\"doi\":\"10.1016/j.xinn.2024.100721\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cough is a vital defensive reflex for expelling harmful substances from the airway. The sensory afferents for the cough reflex have been intensively studied. However, the brain mechanisms underlying the cough reflex remain poorly understood. Here, we developed a paradigm to quantitatively measure cough-like reflexes in mice. Using this paradigm, we found that <i>prodynorphin</i>-expressing (<i>Pdyn</i>+) neurons in the nucleus of the solitary tract (NTS) are critical for capsaicin-induced cough-like reflexes. These neurons receive cough-related neural signals from <i>Trpv1</i>+ vagal sensory neurons. The activation of <i>Pdyn</i>+ NTS neurons triggered respiratory responses resembling cough-like reflexes. Among the divergent projections of <i>Pdyn</i>+ NTS neurons, a glutamatergic pathway projecting to the caudal ventral respiratory group (cVRG), the canonical cough center, was necessary and sufficient for capsaicin-induced cough-like reflexes. These results reveal that <i>Pdyn</i>+ NTS neurons, as a key neuronal population at the entry point of the vagus nerve to the brainstem, initiate cough-like reflexes in mice.</p>\",\"PeriodicalId\":36121,\"journal\":{\"name\":\"The Innovation\",\"volume\":\"5 6\",\"pages\":\"100721\"},\"PeriodicalIF\":33.2000,\"publicationDate\":\"2024-10-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11551472/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Innovation\",\"FirstCategoryId\":\"95\",\"ListUrlMain\":\"https://doi.org/10.1016/j.xinn.2024.100721\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/4 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Innovation","FirstCategoryId":"95","ListUrlMain":"https://doi.org/10.1016/j.xinn.2024.100721","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/4 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Brainstem opioid peptidergic neurons regulate cough reflexes in mice.
Cough is a vital defensive reflex for expelling harmful substances from the airway. The sensory afferents for the cough reflex have been intensively studied. However, the brain mechanisms underlying the cough reflex remain poorly understood. Here, we developed a paradigm to quantitatively measure cough-like reflexes in mice. Using this paradigm, we found that prodynorphin-expressing (Pdyn+) neurons in the nucleus of the solitary tract (NTS) are critical for capsaicin-induced cough-like reflexes. These neurons receive cough-related neural signals from Trpv1+ vagal sensory neurons. The activation of Pdyn+ NTS neurons triggered respiratory responses resembling cough-like reflexes. Among the divergent projections of Pdyn+ NTS neurons, a glutamatergic pathway projecting to the caudal ventral respiratory group (cVRG), the canonical cough center, was necessary and sufficient for capsaicin-induced cough-like reflexes. These results reveal that Pdyn+ NTS neurons, as a key neuronal population at the entry point of the vagus nerve to the brainstem, initiate cough-like reflexes in mice.
期刊介绍:
The Innovation is an interdisciplinary journal that aims to promote scientific application. It publishes cutting-edge research and high-quality reviews in various scientific disciplines, including physics, chemistry, materials, nanotechnology, biology, translational medicine, geoscience, and engineering. The journal adheres to the peer review and publishing standards of Cell Press journals.
The Innovation is committed to serving scientists and the public. It aims to publish significant advances promptly and provides a transparent exchange platform. The journal also strives to efficiently promote the translation from scientific discovery to technological achievements and rapidly disseminate scientific findings worldwide.
Indexed in the following databases, The Innovation has visibility in Scopus, Directory of Open Access Journals (DOAJ), Web of Science, Emerging Sources Citation Index (ESCI), PubMed Central, Compendex (previously Ei index), INSPEC, and CABI A&I.