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白三烯受体拮抗剂MK-0679可阻断吸入赖氨酸阿司匹林对阿司匹林敏感哮喘患者诱发的气道阻塞。

The leukotriene-receptor antagonist MK-0679 blocks airway obstruction induced by inhaled lysine-aspirin in aspirin-sensitive asthmatics.

作者信息

Dahlén B, Kumlin M, Margolskee D J, Larsson C, Blomqvist H, Williams V C, Zetterström O, Dahlén S E

机构信息

Dept of Thoracic Medicine, Karolinska Hospital, Stockholm, Sweden.

出版信息

Eur Respir J. 1993 Jul;6(7):1018-26.

PMID:8396534
Abstract

Drugs which block the action or formation of the cysteinyl leukotrienes (LTC4, LTD4 and LTE4) inhibit asthmatic responses evoked by allergen, exercise and cold dry air. The purpose of this study was to determine whether the specific leukotriene-receptor antagonist MK-0679 could block the airway obstruction induced by aspirin (acetylsalicylic acid (ASA)) in aspirin-intolerant asthmatics. Eight asthmatics (mean age 45 yrs), with an average history of asthma and ASA-sensitivity of about 10 yrs duration, were subjected to bronchial provocation with lysine-ASA. Baseline ASA-sensitivity was first determined in an open prestudy session by inhalation of cumulative doses of lysine-ASA to establish the dose of ASA decreasing forced expiratory volume in one second (FEV1) by 20% (PD20). Rechallenge with lysine-ASA was performed on two different occasions, 1 h after oral administration of placebo, or 750 mg of MK-0679, under double-blind conditions, in a randomized, cross-over design. Leukotriene formation was estimated by the measurement of urinary LTE4. The lysine-ASA challenge was highly reproducible (geometric mean for group PD20 being identical for the open prestudy and the placebo session), and was associated with a post-challenge increase in urinary LTE4. In contrast, after MK-0679, there was a rightward shift in the dose response relationship for all eight subjects (median shift being 4.4 fold), with three of the subjects failing to produce a 20% decrease in FEV1 despite inhalation of the highest dose of lysine-ASA feasible to deliver.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

阻断半胱氨酰白三烯(LTC4、LTD4和LTE4)作用或形成的药物可抑制由过敏原、运动和冷干空气诱发的哮喘反应。本研究的目的是确定特异性白三烯受体拮抗剂MK-0679是否能阻断阿司匹林不耐受性哮喘患者由阿司匹林(乙酰水杨酸(ASA))诱发的气道阻塞。8名哮喘患者(平均年龄45岁),哮喘平均病史及ASA敏感性约为10年,接受赖氨酸-ASA支气管激发试验。在开放的预试验阶段,首先通过吸入累积剂量的赖氨酸-ASA来确定基线ASA敏感性,以确定使一秒用力呼气量(FEV1)降低20%的ASA剂量(PD20)。在双盲条件下,采用随机交叉设计,在口服安慰剂或750 mg MK-0679 1小时后,分两次不同时间用赖氨酸-ASA进行再次激发试验。通过测定尿LTE4来估计白三烯的形成。赖氨酸-ASA激发试验具有高度可重复性(开放预试验和安慰剂试验组的PD20几何平均值相同),且与激发试验后尿LTE4增加有关。相比之下,服用MK-0679后,所有8名受试者的剂量反应关系均向右移位(中位移位为4.4倍),其中3名受试者尽管吸入了可行的最高剂量赖氨酸-ASA,FEV1仍未降低20%。(摘要截短于250字)

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