Brune K, Peskar B A
Int J Tissue React. 1985;7(2):97-103.
Leukotriene and prostaglandin production by mouse peritoneal macrophages was investigated. It could be shown that the tumour promoter 12-O-tetradecanoylphorbol-13-acetate, despite initiating the release of prostaglandin E2, had little effect on the release of leukotriene C4-like immunoreactivity. The divalent cation ionophore A 23187 at concentrations between 10(-6) and 10(-8) mol/l initiated prostaglandin as well as leukotriene release. This prostaglandin and leukotriene release could be modulated by drugs. Non-steroidal anti-inflammatory drugs inhibited prostaglandin release but enhanced leukotriene production. The experimental compound BW 755C inhibited prostaglandin and leukotriene production, whereas the antithrombotic compound nafazatrom inhibited the production of leukotriene C4-like immunoreactivity but enhanced the prostaglandin E2 production. Nordihydroguaiaretic acid inhibited prostaglandin and leukotriene production. The results show that the metabolism of arachidonic acid in macrophages via the cyclooxygenase or the lipoxygenase pathway is dependent on the stimulus applied. Both pathways can be inhibited conjointly or selectively by drugs. The experimental system described may be used for assessing the potency of drugs to inhibit the lipoxygenase and the cyclooxygenase pathway of arachidonic acid metabolism.
对小鼠腹腔巨噬细胞中白三烯和前列腺素的生成进行了研究。结果表明,肿瘤促进剂12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯尽管能引发前列腺素E2的释放,但对白三烯C4样免疫反应性的释放影响很小。浓度在10(-6)至10(-8)摩尔/升之间的二价阳离子载体A 23187能引发前列腺素以及白三烯的释放。这种前列腺素和白三烯的释放可被药物调节。非甾体抗炎药抑制前列腺素的释放,但增强白三烯的生成。实验化合物BW 755C抑制前列腺素和白三烯的生成,而抗血栓化合物萘呋胺酯抑制白三烯C4样免疫反应性的生成,但增强前列腺素E2的生成。去甲二氢愈创木酸抑制前列腺素和白三烯的生成。结果表明,巨噬细胞中花生四烯酸通过环氧化酶或脂氧化酶途径的代谢取决于所施加的刺激。这两条途径都可被药物联合或选择性抑制。所描述的实验系统可用于评估药物抑制花生四烯酸代谢的脂氧化酶和环氧化酶途径的效力。