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本文引用的文献

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Cough and expiration reflexes elicited by inhaled irritant gases are intensified in ovalbumin-sensitized mice.吸入刺激性气体引发的咳嗽和呼气反射在卵清蛋白致敏的小鼠中会增强。
Am J Physiol Regul Integr Comp Physiol. 2017 May 1;312(5):R718-R726. doi: 10.1152/ajpregu.00444.2016. Epub 2017 Feb 22.
2
Biomarkers in asthmatic patients: Has their time come to direct treatment?哮喘患者的生物标志物:它们是否已经到了直接用于治疗的阶段?
J Allergy Clin Immunol. 2016 May;137(5):1317-24. doi: 10.1016/j.jaci.2016.03.009.
3
Approach to chronic cough: the neuropathic basis for cough hypersensitivity syndrome.慢性咳嗽的处理方法:咳嗽高敏综合征的神经病理性基础。
J Thorac Dis. 2014 Oct;6(Suppl 7):S699-707. doi: 10.3978/j.issn.2072-1439.2014.08.41.
4
Anatomy and neurophysiology of cough: CHEST Guideline and Expert Panel report.咳嗽的解剖学与神经生理学:CHEST指南与专家小组报告
Chest. 2014 Dec;146(6):1633-1648. doi: 10.1378/chest.14-1481.
5
Expert opinion on the cough hypersensitivity syndrome in respiratory medicine.呼吸医学中咳嗽高敏综合征的专家意见。
Eur Respir J. 2014 Nov;44(5):1132-48. doi: 10.1183/09031936.00218613. Epub 2014 Aug 19.
6
Sensory nerves in lung and airways.肺部和气道的感觉神经。
Compr Physiol. 2014 Jan;4(1):287-324. doi: 10.1002/cphy.c130020.
7
Models and mechanisms of hyperalgesia and allodynia.痛觉过敏和异常性疼痛的模型与机制。
Physiol Rev. 2009 Apr;89(2):707-58. doi: 10.1152/physrev.00025.2008.
8
Mechanisms of eosinophil major basic protein-induced hyperexcitability of vagal pulmonary chemosensitive neurons.嗜酸性粒细胞主要碱性蛋白诱导迷走神经肺化学敏感神经元兴奋性增高的机制
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9
Cough sensors. V. Pharmacological modulation of cough sensors.咳嗽感受器。五、咳嗽感受器的药理学调节。
Handb Exp Pharmacol. 2009(187):99-127. doi: 10.1007/978-3-540-79842-2_6.
10
Immunohistochemical co-localization of transient receptor potential vanilloid (TRPV)1 and sensory neuropeptides in the guinea-pig respiratory system.豚鼠呼吸系统中瞬时受体电位香草酸亚型1(TRPV1)与感觉神经肽的免疫组织化学共定位
Neuroscience. 2006 Sep 1;141(3):1533-43. doi: 10.1016/j.neuroscience.2006.04.073. Epub 2006 Jun 12.

吸入性变应原引起的咳嗽反应可被清醒小鼠中的嗜酸性粒细胞主要碱性蛋白增强。

Cough responses to inhaled irritants are enhanced by eosinophil major basic protein in awake mice.

机构信息

Department of Physiology, University of Kentucky , Lexington, Kentucky.

Department of Dermatology, University of Utah , Salt Lake City, Utah.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2019 Jul 1;317(1):R93-R97. doi: 10.1152/ajpregu.00081.2019. Epub 2019 Apr 17.

DOI:10.1152/ajpregu.00081.2019
PMID:30995073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6692762/
Abstract

A distinct association between airway eosinophilia and chronic cough is well documented. Eosinophil granule-derived cationic proteins, such as major basic protein (MBP), have been shown to activate and enhance the excitability of bronchopulmonary C-fiber sensory nerves, which may then lead to an increase in cough sensitivity. This study was carried out to determine whether cough responses to inhaled irritant gases were altered by delivery of MBP into the airways. An awake mouse moved freely in a recording chamber that was ventilated with a constant flow of air or irritant gas mixture. Cough responses to separate inhalation challenges of sulfur dioxide (SO; 300 and 600 ppm) and ammonia (NH; 0.1 and 0.2%), each for 5-min duration, were measured daily for 3 days before and for up to 8 days after MBP (10-20 µg) instillation into the trachea. During control, inhalations of SO and NH consistently elicited cough responses in a dose-dependent manner. After MBP treatment, cough responses to both SO and NH increased significantly and progressively and reached peaks 2-3 days after the treatment before returning to control level in 3-7 days. In sharp contrast, cough responses to these irritant gases were not affected by the treatment with the vehicle of MBP. These results suggest that the MBP-induced lingering elevation of cough responsiveness may be a contributing factor in the pathogenesis of chronic cough associated with eosinophilic infiltration of the airways.

摘要

气道嗜酸性粒细胞与慢性咳嗽之间存在明显的关联。已经证实,嗜酸性粒细胞颗粒衍生的阳离子蛋白,如主要碱性蛋白(MBP),可以激活和增强支气管肺 C 纤维感觉神经的兴奋性,这可能导致咳嗽敏感性增加。这项研究旨在确定 MBP 递送至气道是否会改变对吸入刺激性气体的咳嗽反应。一只清醒的老鼠在一个记录室中自由移动,该记录室通过恒定流量的空气或刺激性气体混合物进行通气。在 MBP(10-20µg)滴注到气管之前和之后的 3 天内,每天测量对二氧化硫(SO;300 和 600 ppm)和氨(NH;0.1 和 0.2%)的单独吸入挑战的咳嗽反应,每次持续 5 分钟。在对照条件下,SO 和 NH 的吸入一致地以剂量依赖的方式引起咳嗽反应。在 MBP 治疗后,对 SO 和 NH 的咳嗽反应均显著且逐渐增加,并在治疗后 2-3 天达到峰值,然后在 3-7 天内恢复至对照水平。相比之下,这些刺激性气体的咳嗽反应不受 MBP 载体处理的影响。这些结果表明,MBP 诱导的持续性咳嗽反应升高可能是与气道嗜酸性粒细胞浸润相关的慢性咳嗽发病机制的一个因素。