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Am J Respir Cell Mol Biol. 2015 Dec;53(6):844-52. doi: 10.1165/rcmb.2015-0015OC.
2
Are children׳s asthmatic symptoms related to ambient temperature? A panel study in Australia.儿童的哮喘症状与环境温度有关吗?来自澳大利亚的一项面板研究。
Environ Res. 2014 Aug;133:239-45. doi: 10.1016/j.envres.2014.05.032. Epub 2014 Jun 28.
3
Breathing hot humid air induces airway irritation and cough in patients with allergic rhinitis.吸入热而潮湿的空气会引起变应性鼻炎患者的气道刺激和咳嗽。
Respir Physiol Neurobiol. 2014 Jul 1;198:13-9. doi: 10.1016/j.resp.2014.03.013. Epub 2014 Apr 4.
4
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.
5
Bronchoconstriction induced by increasing airway temperature in ovalbumin-sensitized rats: role of tachykinins.卵清蛋白致敏大鼠气道温度升高诱发的支气管收缩:速激肽的作用。
J Appl Physiol (1985). 2013 Sep 1;115(5):688-96. doi: 10.1152/japplphysiol.00491.2013. Epub 2013 Jul 11.
6
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Heat-related emergency hospitalizations for respiratory diseases in the Medicare population.医疗保险人群与呼吸道疾病相关的高温急诊住院情况。
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8
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9
Bronchoconstriction triggered by breathing hot humid air in patients with asthma: role of cholinergic reflex.哮喘患者吸入热湿空气引发的支气管收缩:胆碱能反射的作用。
Am J Respir Crit Care Med. 2012 Jun 1;185(11):1190-6. doi: 10.1164/rccm.201201-0088OC. Epub 2012 Apr 13.
10
Allergic asthmatics show divergent lipid mediator profiles from healthy controls both at baseline and following birch pollen provocation.变应性哮喘患者在基线和花粉激发后均表现出与健康对照组不同的脂质介质谱。
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卵清蛋白致敏大鼠气道温度升高诱导的迷走神经肺C纤维超敏反应。

Hypersensitivity of vagal pulmonary C-fibers induced by increasing airway temperature in ovalbumin-sensitized rats.

作者信息

Lin Yu-Jung, Lin Ruei-Lung, Khosravi Mehdi, Lee Lu-Yuan

机构信息

Departments of Physiology and.

Internal Medicine, University of Kentucky Medical Center, Lexington, Kentucky.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2015 Nov 15;309(10):R1285-91. doi: 10.1152/ajpregu.00298.2015. Epub 2015 Sep 2.

DOI:10.1152/ajpregu.00298.2015
PMID:26333786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4666940/
Abstract

Our recent study has shown that hyperventilation of humidified warm air (HWA) triggered cough and reflex bronchoconstriction in patients with mild asthma. We suggested that a sensitizing effect on bronchopulmonary C-fibers by increasing airway temperature was involved, but direct evidence was lacking. This study was carried out to test the hypothesis that HWA enhances the pulmonary C-fiber sensitivity in Brown-Norway rats sensitized with ovalbumin (Ova). In anesthetized rats, isocapnic hyperventilation of HWA for 3 min rapidly elevated airway temperature to a steady state of 41.7°C. Immediately after the HWA challenge, the baseline fiber activity (FA) of pulmonary C-fibers was markedly elevated in sensitized rats, but not in control rats. Furthermore, the response of pulmonary C-fibers to right atrial injection of capsaicin in sensitized rats was significantly higher than control rats before the HWA challenge, and the response to capsaicin was further amplified after HWA in sensitized rats (ΔFA = 4.51 ± 1.02 imp/s before, and 9.26 ± 1.74 imp/s after the HWA challenge). A similar pattern of the HWA-induced potentiation of the FA response to phenylbiguanide, another chemical stimulant of C-fibers, was also found in sensitized rats. These results clearly demonstrated that increasing airway temperature significantly elevated both the baseline activity and responses to chemical stimuli of pulmonary C-fibers in Ova-sensitized rats. In conclusion, this study supports the hypothesis that the increased excitability of these afferents may have contributed to the cough and reflex bronchoconstriction evoked by hyperventilation of HWA in patients with asthma.

摘要

我们最近的研究表明,对轻度哮喘患者进行温热湿化空气(HWA)过度通气会引发咳嗽和反射性支气管收缩。我们推测这涉及通过升高气道温度对支气管肺C纤维产生致敏作用,但缺乏直接证据。本研究旨在验证以下假设:HWA会增强用卵清蛋白(Ova)致敏的Brown-Norway大鼠的肺C纤维敏感性。在麻醉的大鼠中,对HWA进行等碳酸过度通气3分钟可使气道温度迅速升高至41.7°C的稳定状态。在HWA刺激后立即观察到,致敏大鼠肺C纤维的基线纤维活动(FA)显著升高,而对照大鼠则未出现此现象。此外,在HWA刺激前,致敏大鼠肺C纤维对右心房注射辣椒素的反应明显高于对照大鼠,且在致敏大鼠中,HWA刺激后对辣椒素的反应进一步增强(刺激前ΔFA = 4.51±1.02 imp/s,刺激后为9.26±1.74 imp/s)。在致敏大鼠中还发现了HWA诱导的对另一种C纤维化学刺激物苯乙双胍的FA反应增强的类似模式。这些结果清楚地表明,升高气道温度显著提高了Ova致敏大鼠肺C纤维的基线活动以及对化学刺激的反应。总之,本研究支持以下假设:这些传入神经兴奋性的增加可能导致了哮喘患者HWA过度通气诱发的咳嗽和反射性支气管收缩。