Britton J R, Hanley S P, Tattersfield A E
J Allergy Clin Immunol. 1987 May;79(5):811-6. doi: 10.1016/0091-6749(87)90214-4.
We have compared the effects of the leukotriene (LT) D4 antagonist L-649,923 and placebo on the airway response to antigen challenge in eight men with mild asthma known to have both an early and late response to inhaled antigen. Subjects ingested 1000 mg of L-649,923 or placebo in a randomized, double-blind protocol and, two hours later, inhaled the dose of antigen known to induce a 20% fall in FEV1. Pulmonary function (specific conductance, FEV1, peak expiratory flow rate, and maximal flow at 25% of vital capacity) was measured at intervals before and up to 9 hours after antigen. FEV1 fell in one subject after L-649,923 ingestion. L-649,923 in the other seven subjects caused no change in baseline pulmonary function, a small reduction in the early response to antigen for FEV1, peak expiratory flow rate, and maximal flow at 25% of vital capacity but not for specific airway conductance (six subjects only) and no effect on the late response. The mean maximum fall in FEV1 in the early response was 1.35 L after L-649,923 ingestion and 1.78 after placebo ingestion. This relatively small degree of protection by L-649,923 suggests either that L-649,923 is not a sufficiently potent antagonist to diminish the effect of endogenous LTD4 in vivo or that LTD4 does not play a major role in the airway response to antigen challenge.
我们比较了白三烯(LT)D4拮抗剂L-649,923和安慰剂对8名已知对吸入抗原具有早期和晚期反应的轻度哮喘男性气道对抗原激发反应的影响。受试者按照随机、双盲方案摄入1000 mg的L-649,923或安慰剂,两小时后,吸入已知可导致第一秒用力呼气容积(FEV1)下降20%的抗原剂量。在抗原激发前及激发后长达9小时的时间段内,每隔一段时间测量肺功能(比气道传导率、FEV1、呼气峰值流速以及肺活量25%时的最大流速)。摄入L-649,923后,有一名受试者的FEV1下降。在其他七名受试者中,L-649,923对基线肺功能无影响,对FEV1、呼气峰值流速以及肺活量25%时的最大流速的早期抗原反应有小幅降低,但对比气道传导率无影响(仅六名受试者),对晚期反应也无影响。摄入L-649,923后,早期反应中FEV1的平均最大下降值为1.35 L,摄入安慰剂后为1.78 L。L-649,923这种相对较小程度的保护作用表明,要么是L-649,923作为拮抗剂的效力不足以在体内减弱内源性白三烯D4(LTD4)的作用,要么是LTD4在气道对抗原激发的反应中不发挥主要作用。