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组胺在变应原和腺苷诱导的支气管收缩中的作用。

The role of histamine in allergen and adenosine-induced bronchoconstriction.

作者信息

Rafferty P, Beasley R, Southgate P, Holgate S

出版信息

Int Arch Allergy Appl Immunol. 1987;82(3-4):292-4. doi: 10.1159/000234210.

Abstract

We have investigated the role of histamine in allergen and adenosine-5'-monophosphate (AMP)-induced bronchoconstriction in asthmatic subjects by performing inhalation challenge tests with histamine, AMP and allergen after treatment with placebo or the potent H1 histamine receptor antagonist, terfenadine. Single concentrations of each agonist which had previously been shown to produce a 30% fall in FEV1 were used. After placebo, AMP and histamine both produced rapid bronchoconstriction reaching a maximum within 5 min and returning to within 10% of baseline after 25 min. Terfenadine inhibited this reaction to histamine completely and to AMP by 86%. The response to allergen was slower in onset and was sustained over 45 min and was inhibited 50% by terfenadine. We interpret these results as reflecting the contribution of histamine to the various airway challenges, both histamine and newly generated mediators comprise the response to allergen, whereas AMP selectively enhances mast cell degranulation without affecting the production of arachidonic acid derived mediators.

摘要

我们通过在给予安慰剂或强效H1组胺受体拮抗剂特非那定治疗后,用组胺、腺苷-5'-单磷酸(AMP)和变应原进行吸入激发试验,研究了组胺在哮喘患者变应原和AMP诱导的支气管收缩中的作用。使用了先前已证明可使第一秒用力呼气容积(FEV1)下降30%的每种激动剂的单一浓度。给予安慰剂后,AMP和组胺均引起快速支气管收缩,在5分钟内达到最大值,并在25分钟后恢复至基线的10%以内。特非那定完全抑制了对组胺的这种反应,并使对AMP的反应抑制了86%。对变应原的反应起效较慢,持续45分钟,特非那定使其抑制50%。我们将这些结果解释为反映了组胺对各种气道激发的作用,组胺和新产生的介质均参与对变应原的反应,而AMP选择性增强肥大细胞脱颗粒,而不影响花生四烯酸衍生介质的产生。

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