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特非那定和氟比洛芬对特应性哮喘患者变应原激发后早发和迟发性支气管收缩的抑制作用。

The inhibitory effect of terfenadine and flurbiprofen on early and late-phase bronchoconstriction following allergen challenge in atopic asthma.

作者信息

Hamid M, Rafferty P, Holgate S T

机构信息

Immunopharmacology Group, Southampton General Hospital, U.K.

出版信息

Clin Exp Allergy. 1990 May;20(3):261-7. doi: 10.1111/j.1365-2222.1990.tb02681.x.

Abstract

We have studied the effect of cyclo-oxygenase inhibition and H1-receptor antagonism on the early and late bronchoconstrictor responses to inhaled allergen in mild atopic asthmatics. In the first phase of the study histamine inhalation challenge tests were performed in seven mild, atopic asthmatics 2 h after treatment with placebo or flurbiprofen (50, 100 or 150 mg). Flurbiprofen in these single doses had no effect on histamine reactivity. Ten atopic asthmatics participated in the second phase of the study in which the time course of the bronchoconstrictor response to inhalation of allergen was observed on four separate occasions after treatment with (a) placebo, (b) flurbiprofen, 150 mg, (c) terfenadine 180 mg, and (d) the combination of flurbiprofen and terfenadine. On each occasion subjects inhaled a concentration of allergen (Dermatagaphoides pteronyssinus, grass pollen) that had previously been shown to produce a 30% fall in FEV1 (PC30 allergen). The mean maximum fall in FEV1 during the early reaction was 33.2 +/- 3.3% from the post-saline baseline value following placebo and this was reduced to 27.5 +/- 5.3% after flurbiprofen (n.s.), 20.3 +/- 3.2% after terfenadine (P less than 0.05), and 23.1 +/- 2.3 after the treatment combination (P less than 0.05). Seven subjects developed late asthmatic reactions (LAR) after placebo and in these subjects the mean maximum fall in PEFR during the LAR was reduced from 22.6 +/- 3.1% after placebo to 16.7 +/- 3.2% after flurbiprofen (P less than 0.05), 15.2 +/- 2.3% after terfenadine (P less than 0.05) and 11.5 +/- 3.1% after the treatment combination (P less than 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了环氧化酶抑制和H1受体拮抗作用对轻度特应性哮喘患者吸入变应原后早期和晚期支气管收缩反应的影响。在研究的第一阶段,对7名轻度特应性哮喘患者在给予安慰剂或氟比洛芬(50、100或150毫克)治疗2小时后进行组胺吸入激发试验。这些单剂量的氟比洛芬对组胺反应性没有影响。10名特应性哮喘患者参与了研究的第二阶段,在分别接受以下治疗后观察四次吸入变应原后支气管收缩反应的时间过程:(a)安慰剂,(b)150毫克氟比洛芬,(c)180毫克特非那定,(d)氟比洛芬和特非那定联合用药。每次受试者吸入一定浓度的变应原(屋尘螨、草花粉),该浓度先前已被证明可使第一秒用力呼气容积(FEV1)下降30%(PC30变应原)。安慰剂治疗后早期反应期间FEV1的平均最大下降幅度为盐水激发后基线值的33.2±3.3%,氟比洛芬治疗后降至27.5±5.3%(无统计学意义),特非那定治疗后为20.3±3.2%(P<0.05),联合治疗后为23.1±2.3%(P<0.05)。7名受试者在接受安慰剂治疗后出现了迟发性哮喘反应(LAR),在这些受试者中,LAR期间呼气峰值流速(PEFR)的平均最大下降幅度从安慰剂治疗后的22.6±3.1%降至氟比洛芬治疗后的16.7±3.2%(P<0.05),特非那定治疗后为15.2±2. .3%(P<0.05),联合治疗后为11.5±3.1%(P<0.01)。(摘要截断于250字)

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