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重复性抗原诱导的豚鼠离体肺条收缩是由白三烯介导的。

Repeatable antigen-induced contractions of isolated guinea pig lung strips are mediated by leukotriene.

作者信息

Robichaud L J, Webster K, Thueson D O

出版信息

Int Arch Allergy Appl Immunol. 1986;80(4):427-30. doi: 10.1159/000234093.

Abstract

Lung strips from actively sensitized guinea pigs were repeatedly contracted by antigen (ovalbumin, OA) challenge in the presence of the antihistamine (H1) mepyramine. At lower concentrations of OA, hourly challenges gave reproducible and consistent responses. High-concentration OA resulted in desensitization, with two to six contractions being very weak. The antigen concentration affected not only the force of contraction, but other parameters including the time to peak effect, the protraction of the peak effect, and the repeatability of the force and time to peak. Low concentrations of OA induced a response which peaked by 6-8 min and decreased by about 30% after 15 min, while high-concentration OA resulted in a contraction which peaked later and did not relax. These data suggest that different 'early' and 'late' mediators may be involved depending on the 'activation state' or the mechanisms that predominate in the contraction response as a result of the amount of stimulation by antigen. Leukotriene apparently mediates the peak and the 15-min contraction since both were inhibited completely by FPL-55712 (IC50 = 8 microM) or NDGA (IC50 = 5 microM). These repeated, leukotriene-mediated contractions of isolated lung may mimic the clinical situation (chronic exposure to low amounts of antigen) of allergic disease and may be used to study the modulation of lung responses and desensitization phenomena.

摘要

在抗组胺药(H1)美吡拉敏存在的情况下,用抗原(卵清蛋白,OA)反复刺激主动致敏豚鼠的肺条,可使其收缩。在较低浓度的OA刺激下,每小时一次的刺激能产生可重复且一致的反应。高浓度的OA会导致脱敏,两到六次收缩非常微弱。抗原浓度不仅影响收缩力,还影响其他参数,包括达到峰值效应的时间、峰值效应的持续时间以及收缩力和达到峰值时间的重复性。低浓度的OA诱导的反应在6 - 8分钟达到峰值,15分钟后下降约30%,而高浓度的OA导致的收缩达到峰值的时间较晚且不松弛。这些数据表明,根据抗原刺激量在收缩反应中占主导的“激活状态”或机制不同,可能涉及不同的“早期”和“晚期”介质。白三烯显然介导了峰值和15分钟时的收缩,因为两者都被FPL - 55712(IC50 = 8 microM)或去甲二氢愈创木酸(NDGA,IC50 = 5 microM)完全抑制。分离肺的这些由白三烯介导的反复收缩可能模拟了过敏性疾病的临床情况(长期暴露于少量抗原),可用于研究肺反应的调节和脱敏现象。

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