Mielens Z E, Magro A
Methods Find Exp Clin Pharmacol. 1982;4(2):111-7.
Investigational compounds active in anti-allergic/anti-asthmatic screens in rodents in vivo (IgE-mediated passive cutaneous anaphylaxis in rats, IgE-mediated anaphylactic bronchoconstriction in guinea pigs, and histamine-, or acetylcholine-induced bronchoconstriction in guinea pigs) were examined for their effects against IgE-mediated histamine release from human basophiles. Fifty-seven% (19/33) of investigational compounds active against passive cutaneous anaphylaxis in rats and 40% (12/30) of compounds active against anaphylactic bronchoconstriction in guinea pigs were active also against histamine release from human basophiles. Twenty-eight percent (8/29) and 38% (6/15) of compounds active agonist histamine- and acetylcholine-bronchoconstriction in guinea pigs, respectively, were active also against histamine release from human basophiles. The lack of consistent activity of investigational compounds in the in vivo IgE-mediated anaphylactic screens suggests that diverse inhibitory mechanisms are involved. Anaphylactic histamine release from human basophiles may serve as an adjunct in the determination of the activity profiles of new antiallergic agents. It is of limited value in the search for new bronchodilators.
对在啮齿动物体内抗过敏/抗哮喘筛选试验(大鼠体内IgE介导的被动皮肤过敏反应、豚鼠体内IgE介导的过敏性支气管收缩以及豚鼠体内组胺或乙酰胆碱诱导的支气管收缩)中有活性的研究性化合物,检测其对人嗜碱性粒细胞IgE介导的组胺释放的影响。对大鼠被动皮肤过敏反应有活性的研究性化合物中,57%(19/33)以及对豚鼠过敏性支气管收缩有活性的化合物中,40%(12/30)对人嗜碱性粒细胞组胺释放也有活性。分别对豚鼠组胺和乙酰胆碱诱导的支气管收缩有活性的化合物中,28%(8/29)和38%(6/15)对人嗜碱性粒细胞组胺释放也有活性。研究性化合物在体内IgE介导的过敏筛选试验中缺乏一致的活性,这表明涉及多种抑制机制。人嗜碱性粒细胞过敏性组胺释放可作为确定新型抗过敏药物活性谱的辅助手段。在寻找新型支气管扩张剂方面价值有限。