Andersson P
Br J Pharmacol. 1982 Oct;77(2):301-7. doi: 10.1111/j.1476-5381.1982.tb09299.x.
1 The effects of pretreatment with various inhibitors of anaphylactic mediators on antigen-induced bronchoconstriction were studied in anaesthetized guinea-pigs, actively sensitized according to two different regimens (one producing IgE- and IgG-like antibodies and the other producing exclusively IgG antibodies).2 The phospholipase A(2)-inhibitors mepacrine and p-bromphenacylbromide caused a dose-dependent inhibition of the antigen-induced bronchoconstriction in guinea-pigs sensitized to produce both IgE and IgG antibodies. No effect was seen in those sensitized to produce only IgG antibodies.3 In both models indomethacin pretreatment led to an increased anaphylactic bronchoreactivity, whereas mepyramine and FPL 55712 reduced it.4 BW 755C significantly reduced antigen-induced bronchoconstriction in guinea-pigs sensitized to produce both IgE and IgG antibodies. In this model, the residual bronchoconstriction evident after combined pretreatment with indomethacin and mepyramine was prevented by additional pretreatment with mepacrine, FPL 55712 or budesonide.5 Arachidonic acid given intravenously caused a marked bronchoconstriction that was prevented by indomethacin but not by budesonide, FPL 55712 or p-bromphenacylbromide.6 Although the same pattern of anaphylactic mediators is released in the two models of anaphylactic bronchoconstriction, a different activation mechanism is indicated by the results obtained with phospholipase A(2) inhibitors.
在麻醉的豚鼠中研究了用各种过敏介质抑制剂预处理对抗原诱导的支气管收缩的影响,这些豚鼠根据两种不同方案进行主动致敏(一种产生IgE和IgG样抗体,另一种仅产生IgG抗体)。
磷脂酶A(2)抑制剂米帕林和对溴苯甲酰溴在对产生IgE和IgG抗体均致敏的豚鼠中引起抗原诱导的支气管收缩的剂量依赖性抑制。在仅对产生IgG抗体致敏的豚鼠中未观察到效果。
在两种模型中,吲哚美辛预处理均导致过敏支气管反应性增加,而美吡拉敏和FPL 55712则使其降低。
BW 755C显著降低了对产生IgE和IgG抗体均致敏的豚鼠中抗原诱导的支气管收缩。在该模型中,吲哚美辛和美吡拉敏联合预处理后明显的残余支气管收缩可通过米帕林、FPL 55712或布地奈德的额外预处理来预防。
静脉注射花生四烯酸引起明显的支气管收缩,吲哚美辛可预防,但布地奈德、FPL 55712或对溴苯甲酰溴不能预防。
尽管在两种过敏性支气管收缩模型中释放的过敏介质模式相同,但磷脂酶A(2)抑制剂的结果表明存在不同的激活机制。