Rasmussen J B, Eriksson L O, Andersson K E
Department of Pulmonary Medicine, University of Lund, Malmö General Hospital, Sweden.
Allergy. 1991 May;46(4):266-73. doi: 10.1111/j.1398-9995.1991.tb00584.x.
We examined the ability of the inhaled leukotriene D4 antagonist (L-648,051) to inhibit antigen-induced asthmatic responses. Twelve patients with stable exogenous asthma participated in two separate double-blind, placebo-controlled, cross-over trials. The ability of the antagonist to reverse or inhibit antigen-induced bronchoconstrictor response was examined; both the immediate and the late phases were studied. In the reversal study, patients inhaled 800 micrograms of L-648,051 during the immediate phase (15 min after antigen challenge) and again during in the late phase (7 h after antigen challenge). In the prevention study, the same dose (800 micrograms) of L-648,051 was inhaled before the expected immediate reaction (5 min before antigen challenge) as well as before the expected late reaction (2.5 h after antigen challenge). The LTD4 antagonist was not effective in reversing the airway response to inhaled antigen, as measured by airway resistance (Rt), forced expiratory volume in 1 s (FEV1) or forced vital capacity (FVC). When the antagonist was given prior to antigen challenge, a slight reduction in Rt was observed during the immediate phase, but not during the late phase. Some improvement in FEV1 and FVC during the immediate phase was also observed, but these changes did not reach statistical significance. These results suggest that LTD4 plays a role in the immediate phase of antigen-induced asthma.
我们研究了吸入性白三烯D4拮抗剂(L-648,051)抑制抗原诱导的哮喘反应的能力。12名稳定期外源性哮喘患者参与了两项独立的双盲、安慰剂对照、交叉试验。检测了该拮抗剂逆转或抑制抗原诱导的支气管收缩反应的能力;同时研究了速发相和迟发相。在逆转研究中,患者在速发相(抗原激发后15分钟)和迟发相(抗原激发后7小时)各吸入800微克L-648,051。在预防研究中,在预期的速发反应前(抗原激发前5分钟)以及预期的迟发反应前(抗原激发后2.5小时)吸入相同剂量(800微克)的L-648,051。以气道阻力(Rt)、第1秒用力呼气容积(FEV1)或用力肺活量(FVC)衡量,LTD4拮抗剂在逆转气道对吸入抗原的反应方面无效。当在抗原激发前给予该拮抗剂时,在速发相观察到Rt略有降低,但在迟发相未观察到。在速发相也观察到FEV1和FVC有一些改善,但这些变化未达到统计学显著性。这些结果表明LTD4在抗原诱导的哮喘速发相中起作用。