Lagente V, Boichot E, Carre C, Guinot P, Mencia-Huerta J M, Braquet P
Institut Henri Beaufour, Les Ulis, France.
Clin Exp Allergy. 1993 Dec;23(12):1002-10. doi: 10.1111/j.1365-2222.1993.tb00291.x.
The involvement of platelet activating factor (PAF) in antigen-induced bronchial hyperresponsiveness was investigated by the use of the PAF antagonists BN 52021 and BN 50730, in a guinea-pig model where sensitization and challenge were performed by aerosol. Male Hartley guinea-pigs were sensitized by two aerosol exposures at 48 hr intervals to a 0.9% NaCl solution (saline) containing 2 mg/ml ovalbumin for 30 min. Fifteen to 20 days later, guinea-pigs were challenged by exposure to five successive aerosols of increasing concentrations of ovalbumin (OA) or respectively, 10 microg/ml, 100 microg/ml, 1 mg/ml, 5 mg/ml and 10 mg/ml for 15 min each, or saline alone. Three to four hr and 18-24 hr after the aerosol challenge the guinea-pigs were prepared for recording of bronchopulmonary response and aerosol administrations were then generated with an ultrasonic nebulizer. The bronchopulmonary responses induced by successive 1-min aerosol bursts of acetylcholine (ACh) was assessed. As compared with saline-challenged guinea-pigs, an enhanced bronchopulmonary response to aerosol administration of cumulative doses of ACh was observed, 3-4 hr and 18-24 hr post-ovalbumin challenge. When the sensitized guinea-pigs were pretreated 1 hr before ovalbumin exposure with BN 52021 or BN 50730 (25 mg/kg, per os), a significant inhibition of the increase in the bronchopulmonary response to ACh was observed, both at 3-4 hr and 18-24 hr. Furthermore, when guinea-pigs were treated 3-4 hr after the ovalbumin exposure with BN 52021 or BN 50730, a significant inhibition of the hyperresponsiveness to ACh was recorded at 18-24 hr. A marked accumulation of eosinophils in the peribronchial regions was observed on histological preparations of lung specimens collected 4 hr or 24 hr after ovalbumin exposure. Pretreatment of the guinea-pigs by BN 50730 or BN 52021 did not modify the eosinophil accumulation in the peribronchial area. No significant difference in the number of eosinophils collected in the bronchoalveolar lavage fluid is observed, 24 hr post-ovalbumin challenge, under the pretreatment with BN 52021 or BN 50730. Pretreatment of guinea-pigs by BN 50730 or BN 52021 significantly reduced the PAF-induced (100 microg/ml) increase in eosinophil number in the peribronchial area. By contrast, they did not inhibit the eosinophilia induced by aerosol administration of LTB4 (5 microg/ml). These results suggest that the bronchial hyperresponsiveness observed in this study is associated with eosinophil accumulation in the lung. The potent inhibition of the bronchial hyperresponsiveness by the two unrelated antagonists of PAF suggests that the lipid mediator is involved in its triggering and duration, but not in the eosinophil infiltration.
通过使用血小板活化因子(PAF)拮抗剂BN 52021和BN 50730,在豚鼠模型中研究PAF在抗原诱导的支气管高反应性中的作用,该模型通过气溶胶进行致敏和激发。雄性Hartley豚鼠每隔48小时通过气溶胶暴露于含有2 mg/ml卵清蛋白的0.9%氯化钠溶液(生理盐水)中30分钟,进行两次致敏。15至20天后,豚鼠分别暴露于浓度递增的五次连续卵清蛋白(OA)气溶胶中,即10μg/ml、100μg/ml、1mg/ml、5mg/ml和10mg/ml,每次15分钟,或仅暴露于生理盐水。在气溶胶激发后3至4小时和18至24小时,将豚鼠准备好记录支气管肺反应,然后用超声雾化器产生气溶胶给药。评估连续1分钟乙酰胆碱(ACh)气溶胶脉冲诱导的支气管肺反应。与生理盐水激发的豚鼠相比,在卵清蛋白激发后3至4小时和18至24小时,观察到对累积剂量ACh气溶胶给药的支气管肺反应增强。当致敏豚鼠在卵清蛋白暴露前1小时用BN 52021或BN 50730(25mg/kg,口服)预处理时,在3至4小时和18至24小时均观察到对ACh支气管肺反应增加的显著抑制。此外,当豚鼠在卵清蛋白暴露后3至4小时用BN 52021或BN 50730治疗时,在18至24小时记录到对ACh高反应性的显著抑制。在卵清蛋白暴露后4小时或24小时收集的肺标本组织学切片上,观察到支气管周围区域嗜酸性粒细胞明显聚集。用BN 50730或BN 52021对豚鼠进行预处理并未改变支气管周围区域嗜酸性粒细胞的聚集。在卵清蛋白激发后24小时,用BN 52021或BN 50730预处理后,支气管肺泡灌洗液中收集的嗜酸性粒细胞数量没有显著差异。用BN 50730或BN 52021对豚鼠进行预处理显著降低了PAF诱导的(100μg/ml)支气管周围区域嗜酸性粒细胞数量的增加。相比之下,它们并未抑制气溶胶给予白三烯B4(LTB4,5μg/ml)诱导的嗜酸性粒细胞增多。这些结果表明,本研究中观察到的支气管高反应性与肺中嗜酸性粒细胞聚集有关。两种不相关的PAF拮抗剂对支气管高反应性的有效抑制表明,这种脂质介质参与了其触发和持续过程,但不参与嗜酸性粒细胞浸润。