Trocklé G, Catau G, Kalt C, Jacque M
J Pharmacol. 1986 Apr-Jun;17(2):163-5.
The effects of selective inhibitions of both cyclo-oxygenase and lipoxygenase pathways were studied in the isolated, perfused and ventilated guinea-pig lungs. Leukotriene D4 (0.3 nmol) induced a significant bronchoconstriction. This effect was significantly inhibited by IPL 55712 (a SRS-A antagonist) and by Imidazole or Dazoxiben (specific thromboxane synthetase inhibitors), but aspirin and indomethacin were without significant effect on this broncho-constriction. Our results suggest that the principal component of leukotriene D4 induced bronchoconstriction in guinea-pig lungs is primary.
在离体、灌注和通气的豚鼠肺中研究了环氧化酶和脂氧合酶途径选择性抑制的作用。白三烯D4(0.3纳摩尔)引起显著的支气管收缩。IPL 55712(一种慢反应物质A拮抗剂)以及咪唑或达唑氧苯(特异性血栓素合成酶抑制剂)可显著抑制此作用,但阿司匹林和吲哚美辛对此支气管收缩无显著影响。我们的结果表明,白三烯D4诱导豚鼠肺支气管收缩的主要成分是原发性的。