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Allergen-induced increase in bronchial responsiveness to histamine: relationship to the late asthmatic response and change in airway caliber.变应原诱导的支气管对组胺反应性增加:与迟发性哮喘反应及气道管径变化的关系。
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Platelet-activating factor: a possible mediator of the dual response to allergen?
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Urinary N tau-methylhistamine during early and late allergen-induced bronchial-obstructive reactions.变应原诱导的早期和晚期支气管阻塞反应期间的尿N-甲基组胺
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Bronchoalveolar eosinophilia during allergen-induced late asthmatic reactions.变应原诱导的迟发型哮喘反应期间的支气管肺泡嗜酸性粒细胞增多
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Prediction of airway responsiveness to allergen from skin sensitivity to allergen and airway responsiveness to histamine.根据对变应原的皮肤敏感性和对组胺的气道反应性预测气道对变应原的反应性。
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Pharmacological actions of WEB 2086, a new specific antagonist of platelet activating factor.血小板活化因子新型特异性拮抗剂WEB 2086的药理作用
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Platelet-activating factor as a mediator of allergic disease.
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Mechanism of platelet activating factor-induced bronchoconstriction in humans.血小板活化因子诱导人类支气管收缩的机制。
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血小板活化因子拮抗剂WEB 2086对变应原诱导的哮喘反应的影响。

Effect of a platelet activating factor antagonist, WEB 2086, on allergen induced asthmatic responses.

作者信息

Freitag A, Watson R M, Matsos G, Eastwood C, O'Byrne P M

机构信息

Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Thorax. 1993 Jun;48(6):594-8. doi: 10.1136/thx.48.6.594.

DOI:10.1136/thx.48.6.594
PMID:8346486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC464572/
Abstract

BACKGROUND

Platelet activating factor (PAF) has been implicated in the pathogenesis of airway hyperresponsiveness in asthma. The purpose of this study was to evaluate the effects of a selective PAF antagonist (WEB 2086), given in doses known to antagonise the effects of inhaled PAF in human subjects, on allergen induced early and late asthmatic responses and on airway hyperresponsiveness.

METHODS

Eight atopic, mildly asthmatic subjects were studied during a screening period and two treatment periods. During the screening period subjects inhaled an allergen to which they were known to be sensitised and the response was measured as the fall in the forced expired volume in one second (FEV1) to show the presence of early (0-1 h) and late (3-7 h) asthmatic responses. On another day the subjects inhaled allergen diluent. During the treatment periods subjects inhaled allergen after one week's pretreatment with WEB 2086 (100 mg three times a day) or placebo administered in a randomised, double blind, crossover fashion. Histamine airway responsiveness was measured 24 hours before and 24 hours after allergen and the results were expressed as the provocative concentration causing a 20% fall in FEV1 (PC20).

RESULTS

The maximal early asthmatic response after allergen with placebo treatment was 18.4% (SE 4.4%) and with WEB 2086 18.9% (4.4%). The maximal late response with placebo treatment was 21.7% (5.3%) and with WEB 2086 21.2% (3.0%). The log difference (before and after allergen) in histamine PC20 was 0.35 (0.06) after placebo treatment and 0.30 (0.1) after WEB 2086.

CONCLUSIONS

These results indicate that one week of treatment with an orally administered PAF antagonist (WEB 2086) does not attenuate allergen induced early or late responses or airway hyperresponsiveness.

摘要

背景

血小板活化因子(PAF)与哮喘气道高反应性的发病机制有关。本研究的目的是评估一种选择性PAF拮抗剂(WEB 2086)对变应原诱导的哮喘早期和晚期反应以及气道高反应性的影响,其给药剂量已知可拮抗吸入PAF对人体的作用。

方法

对8名特应性轻度哮喘患者在筛查期和两个治疗期进行研究。在筛查期,患者吸入已知对其致敏的变应原,并以一秒用力呼气容积(FEV1)下降来衡量反应,以显示早期(0 - 1小时)和晚期(3 - 7小时)哮喘反应的存在。在另一天,患者吸入变应原稀释剂。在治疗期,患者在接受一周的WEB 2086(100毫克,每日三次)或安慰剂预处理后,以随机、双盲、交叉方式吸入变应原。在变应原前后24小时测量组胺气道反应性,结果以引起FEV1下降20%的激发浓度(PC20)表示。

结果

安慰剂治疗后变应原激发后的最大早期哮喘反应为18.4%(标准误4.4%),WEB 2086治疗后为18.9%(4.4%)。安慰剂治疗后的最大晚期反应为21.7%(5.3%),WEB 2086治疗后为21.2%(3.0%)。安慰剂治疗后组胺PC20(变应原前后)的对数差值为0.35(0.06),WEB 2086治疗后为0.30(0.1)。

结论

这些结果表明,口服PAF拮抗剂(WEB 2086)治疗一周并不能减轻变应原诱导的早期或晚期反应或气道高反应性。