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A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity

Chronic cough is a common refractory symptom of various respiratory diseases. However, the neural mechanisms that modulate the cough sensitivity and mediate chronic cough remain elusive. Here, we report that GABAergic neurons in the lateral/ventrolateral periaqueductal gray (l/vlPAG) suppress cough...

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Detalles Bibliográficos
Autores principales: Chen, Zhe, Lin, Ming-Tong, Zhan, Chen, Zhong, Nan-Shan, Mu, Di, Lai, Ke-Fang, Liu, Mingzhe J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741493/
https://www.ncbi.nlm.nih.gov/pubmed/35028531
http://dx.doi.org/10.1016/j.isci.2021.103641
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author Chen, Zhe
Lin, Ming-Tong
Zhan, Chen
Zhong, Nan-Shan
Mu, Di
Lai, Ke-Fang
Liu, Mingzhe J.
author_facet Chen, Zhe
Lin, Ming-Tong
Zhan, Chen
Zhong, Nan-Shan
Mu, Di
Lai, Ke-Fang
Liu, Mingzhe J.
author_sort Chen, Zhe
collection PubMed
description Chronic cough is a common refractory symptom of various respiratory diseases. However, the neural mechanisms that modulate the cough sensitivity and mediate chronic cough remain elusive. Here, we report that GABAergic neurons in the lateral/ventrolateral periaqueductal gray (l/vlPAG) suppress cough processing via a descending pathway. We found that l/vlPAG neurons are activated by coughing-like behaviors and that tussive agent-evoked coughing-like behaviors are impaired after activation of l/vlPAG neurons. In addition, we showed that l/vlPAG neurons form inhibitory synapses with the nucleus of the solitary tract (NTS) neurons. The synaptic strength of these inhibitory projections is weaker in cough hypersensitivity model mice than in naïve mice. Important, activation of l/vlPAG GABAergic neurons projecting to the NTS decreases coughing-like behaviors. In contrast, suppressing these neurons enhances cough sensitivity. These results support the notion that l/vlPAG GABAergic neurons play important roles in cough hypersensitivity and chronic cough through disinhibition of cough processing at the medullary level.
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spelling pubmed-87414932022-01-12 A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity Chen, Zhe Lin, Ming-Tong Zhan, Chen Zhong, Nan-Shan Mu, Di Lai, Ke-Fang Liu, Mingzhe J. iScience Article Chronic cough is a common refractory symptom of various respiratory diseases. However, the neural mechanisms that modulate the cough sensitivity and mediate chronic cough remain elusive. Here, we report that GABAergic neurons in the lateral/ventrolateral periaqueductal gray (l/vlPAG) suppress cough processing via a descending pathway. We found that l/vlPAG neurons are activated by coughing-like behaviors and that tussive agent-evoked coughing-like behaviors are impaired after activation of l/vlPAG neurons. In addition, we showed that l/vlPAG neurons form inhibitory synapses with the nucleus of the solitary tract (NTS) neurons. The synaptic strength of these inhibitory projections is weaker in cough hypersensitivity model mice than in naïve mice. Important, activation of l/vlPAG GABAergic neurons projecting to the NTS decreases coughing-like behaviors. In contrast, suppressing these neurons enhances cough sensitivity. These results support the notion that l/vlPAG GABAergic neurons play important roles in cough hypersensitivity and chronic cough through disinhibition of cough processing at the medullary level. Elsevier 2021-12-16 /pmc/articles/PMC8741493/ /pubmed/35028531 http://dx.doi.org/10.1016/j.isci.2021.103641 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Chen, Zhe
Lin, Ming-Tong
Zhan, Chen
Zhong, Nan-Shan
Mu, Di
Lai, Ke-Fang
Liu, Mingzhe J.
A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title_full A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title_fullStr A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title_full_unstemmed A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title_short A descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
title_sort descending pathway emanating from the periaqueductal gray mediates the development of cough-like hypersensitivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741493/
https://www.ncbi.nlm.nih.gov/pubmed/35028531
http://dx.doi.org/10.1016/j.isci.2021.103641
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