Suppr超能文献

特非那定(思立安)是一种强效且具有选择性的组胺H1受体拮抗剂,作用于哮喘气道。

Terfenadine (Seldane) is a potent and selective histamine H1 receptor antagonist in asthmatic airways.

作者信息

Rafferty P, Holgate S T

出版信息

Am Rev Respir Dis. 1987 Jan;135(1):181-4. doi: 10.1164/arrd.1987.135.1.181.

Abstract

Terfenadine (Seldane) is a new, highly potent H1 histamine receptor antagonist that in clinically effective doses is free of side effects. Because the low potency and specificity of many H1 receptor antagonists have made it difficult to define the precise role of histamine as a bronchoconstrictor mediator in asthma we have used terfenadine to define the degree and selectivity of H1 blockade that can be achieved in asthmatic airways. In a double-blind study, 9 asthmatic patients received placebo or terfenadine 60, 120, and 180 mg on separate days followed 3 h later by bronchial provocation with increasing concentrations of either histamine or methacholine. Terfenadine at 60, 120, and 180 mg produced significant bronchodilation with increases in FEV1 above baseline of 9.0, 9.5, and 10%, respectively (p less than 0.05, p less than 0.01, p less than 0.01). All 3 doses of terfenadine displaced the histamine-FEV1 concentration response curves in a parallel fashion to the right in all subjects. When the degree of protection against histamine is expressed as a concentration ratio, terfenadine 60, 120, and 180 mg displaced the response curves by factors of 14.8 +/- 4.6, 22.9 +/- 6.7, and 34.3 +/- 8.4. In contrast to its effect on histamine-induced bronchoconstriction, terfenadine failed to protect the airways against the constrictor effect of inhaled methacholine. Thus, terfenadine is a much more potent and selective H1 receptor antagonist in asthmatic airways than previously available antihistamines and should provide a powerful tool to define the contribution of histamine as a bronchoconstrictor mediator in asthma.

摘要

特非那定(赛特赞)是一种新型、高效的H1组胺受体拮抗剂,临床有效剂量时无副作用。由于许多H1受体拮抗剂效力低且特异性不强,难以明确组胺作为哮喘中支气管收缩介质的确切作用,我们使用特非那定来确定在哮喘气道中可实现的H1受体阻断程度和选择性。在一项双盲研究中,9名哮喘患者在不同日期分别接受安慰剂或60、120和180毫克特非那定,3小时后用浓度递增的组胺或乙酰甲胆碱进行支气管激发试验。60、120和180毫克特非那定都产生了显著的支气管扩张,第一秒用力呼气量(FEV1)分别比基线增加了9.0%、9.5%和10%(p<0.05,p<0.01,p<0.01)。所有3个剂量的特非那定都使所有受试者的组胺-FEV1浓度反应曲线以平行方式向右移动。当以浓度比表示对组胺的保护程度时,60、120和180毫克特非那定使反应曲线移动的系数分别为14.8±4.6、22.9±6.7和34.3±8.4。与它对组胺诱导的支气管收缩的作用相反,特非那定未能保护气道免受吸入乙酰甲胆碱的收缩作用。因此,在哮喘气道中,特非那定是一种比以前可用的抗组胺药更有效、更具选择性的H1受体拮抗剂,应该能为确定组胺作为哮喘中支气管收缩介质的作用提供有力工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验