Eicosanoids modulate hyperpnea-induced late phase airway obstruction and hyperreactivity in dogs

被引:7
作者
Davis, MS
McCulloch, S
Myers, T
Freed, AN
机构
[1] Oklahoma State Univ, Dept Physiol Sci, Stillwater, OK 74078 USA
[2] Johns Hopkins Med Inst, Sch Hyg & Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
来源
RESPIRATION PHYSIOLOGY | 2002年 / 129卷 / 03期
关键词
airways; obstruction; hyperpnea-induced; disease; asthma; hyperreactivity; mammals; dogs; mediators; eicosanoids; histamine; pharmacological agents; cyclooxygenase inhibitors; prmacological agents; lipoxygenase inhibitors; ventilation; hyperpnea-induced late phase airway obstruction;
D O I
10.1016/S0034-5687(01)00317-6
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A canine model of exercise-induced asthma was used to test the hypothesis that the development of a late phase response to hyperventilation depends on the acute production of pro-inflammatory mediators. Peripheral airway resistance, reactivity to hypocapnia and aerosol histamine, and bronchoalveolar lavage fluid (BALF) cell and eicosanoid content were measured in dogs similar to5 h after dry air challenge (DAC). DAC resulted in late phase obstruction, hyperreactivity to histamine, and neutrophilic inflammation. Both cyclooxygenase and lipoxygenase inhibitors administered in separate experiments attenuated the late phase airway obstruction and hyperreactivity to histamine. Neither drug affected the late phase inflammation nor the concentrations of eicosanoids in the BALF obtained 5 h after DAC. This study confirms that hyperventilation of peripheral airways with unconditioned air causes late phase neutrophilia, airway obstruction, and hyperreactivity. The late phase changes in airway mechanics are related to the hyperventilation-induced release of both prostaglandins and leukotrienes, and appear to be independent of the late phase infiltration of inflammatory cells. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:357 / 365
页数:9
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