Wang C G, Du T, Xu L J, Martin J G
Meakins-Christie Laboratories, McGill University, Montreal, Quebec, Canada.
Am Rev Respir Dis. 1993 Aug;148(2):413-7. doi: 10.1164/ajrccm/148.2.413.
The purpose of the study was to investigate whether allergen-induced hyperresponsiveness to methacholine and an increase in airway smooth muscle (ASM) in Brown Norway (BN) rats could be mediated by LTD4, an important mediator of allergic airway responses. Male BN rats, 8 to 12 wk of age, were sensitized with ovalbumin (OA). Rats were exposed 2 wk later to aerosols of saline (n = 6), OA (n = 8), or OA after pretreatment with the LTD4 antagonist MK-571 (2 mg/kg intraperitoneally, n = 9), on six occasions at 5-day intervals. Airway responsiveness to methacholine (the concentration required to double pulmonary resistance, EC200 RL) was measured immediately before the first aerosol exposure and 2 days after the last exposure. ASM was quantitated by morphometry, and areas were standardized for size using the epithelial basement membrane length (BM). Following OA challenges EC200 RL decreased from 6.5 to 3.1 mg/ml (p < 0.05) but did not change significantly after saline or OA exposures in MK-571-pretreated animals. ASM/BM2 in the large airways was significantly greater, 3.41 +/- 0.19 x 10(-3), after OA compared with 2.35 +/- 0.22 x 10(-3) for saline exposures (p < 0.01). The ASM/BM2 after OA exposures but with MK-571 pretreatment (2.75 +/- 0.25 x 10(-3)) was intermediate in value. The results indicate that both the increase in airway responsiveness and the increase in ASM following repeated antigen exposures appear to be mediated predominantly by LTD4.
本研究的目的是调查变应原诱导的对乙酰甲胆碱的高反应性以及棕色挪威(BN)大鼠气道平滑肌(ASM)的增加是否可由白三烯D4(LTD4)介导,LTD4是过敏性气道反应的一种重要介质。8至12周龄的雄性BN大鼠用卵清蛋白(OA)致敏。2周后,大鼠每隔5天接受6次盐水气雾剂(n = 6)、OA气雾剂(n = 8)或LTD4拮抗剂MK-571预处理(腹腔注射2 mg/kg,n = 9)后的OA气雾剂暴露。在第一次气雾剂暴露前和最后一次暴露后2天测量气道对乙酰甲胆碱的反应性(使肺阻力加倍所需的浓度,EC200 RL)。通过形态计量法定量ASM,并使用上皮基底膜长度(BM)对面积进行大小标准化。在OA激发后,EC200 RL从6.5降至3.1 mg/ml(p < 0.05),但在MK-571预处理的动物中,盐水或OA暴露后无显著变化。与盐水暴露时的2.35 +/- 0.22 x 10(-3)相比,OA后大气道中的ASM/BM2显著更高,为3.41 +/- 0.19 x 10(-3)(p < 0.01)。OA暴露但经MK-571预处理后的ASM/BM2(为2.75 +/- 0.25 x 10(-3))处于中间值。结果表明,反复抗原暴露后气道反应性的增加和ASM的增加似乎主要由LTD4介导。