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豚鼠免疫复合物诱导支气管收缩的药理学特征

Pharmacologic characterization of immune complex induced bronchoconstriction in guinea pigs.

作者信息

Mielens Z E, Ferguson E W, Ferrari R A

出版信息

Agents Actions. 1981 Dec;11(6-7):673-8. doi: 10.1007/BF01978788.

Abstract

Intravenous injections of soluble immune complexes to anesthetized guinea pigs resulted in bronchoconstriction that was inhibited by FPL 55712, indomethacin, oxarbazole, soybean trypsin inhibitor, and cobra venom factor. Immune complex induced bronchoconstriction was not inhibited by atropine, imidazole, mepyramine, ketotifen, methysergide, and the anti-anaphylactic compound DPP (Diethyl [2-(4-pyridyl)-4-pyrimidinyl]aminoethylene malonate). Immune complex induced bronchoconstriction in guinea pigs appears to involve activation of complement and formation of anaphylatoxins. In addition, products of cyclo-oxygenase metabolism of arachidonic acid and kinins may be involved.

摘要

向麻醉的豚鼠静脉注射可溶性免疫复合物会导致支气管收缩,FPL 55712、吲哚美辛、奥沙唑、大豆胰蛋白酶抑制剂和眼镜蛇毒因子可抑制这种收缩。免疫复合物诱导的支气管收缩不受阿托品、咪唑、美吡拉敏、酮替芬、甲基麦角新碱和抗过敏化合物DPP(丙二酸二乙酯[2-(4-吡啶基)-4-嘧啶基]氨基乙烯酯)的抑制。免疫复合物诱导豚鼠支气管收缩似乎涉及补体激活和过敏毒素的形成。此外,花生四烯酸的环氧化酶代谢产物和激肽可能也参与其中。

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