Yamamoto A, Shikada K, Tanaka S
Shiraoka Research Station of Biological Science, Nissan Chemical Ind. Ltd., Saitama, Japan.
Prostaglandins. 1990 Dec;40(6):615-25. doi: 10.1016/0090-6980(90)90006-h.
We compared the effects of the leukotriene (LT) D4 receptor antagonist FPL55712 and some lipoxygenase inhibitors on contractions of isolated guinea-pig trachea induced by antigen (ovalbumin, OA) and calcium ionophore A23187 in the presence of the cyclooxygenase inhibitor indomethacin (5 microM), and by arachidonic acid (AA), melittin and LTD4. FPL55712 (0.1 and 1 microM) inhibited contractions induced by AA (100 microM) and the phospholipase A2 activator melittin (3 micrograms/ml), while the lipoxygenase inhibitor nordihydroguaiaretic acid (NDGA, 10 microM) was a more effective inhibitor of the melittin response than the AA response. FPL55712 inhibited contractions induced by OA (100 micrograms/ml) more than by A23187 (1 microgram/ml), and these inhibitory effects of FPL55712 were much less in the presence of l-serine-borate complex (45 mM), an inhibitor of LTC4 conversion to LTD4. NDGA (10 microM) had no significant effect on the OA response, whereas the lipoxygenase inhibitors 1-phenyl-3-pyrazolidone (phenidone, 10 microM) and 5,8,11,14-eicosatetraynoic acid (ETYA, 10 microM) clearly inhibited it. In contrast, NDGA and phenidone inhibited the A23187 response, but ETYA had no effect on it. FPL55712, phenidone and ETYA, but not NDGA, had a large inhibitory effect on LTD4-induced contractions, but these inhibitors had no effect on histamine-induced contractions. These results suggest that in the guinea-pig trachea inhibitors of LTD4-induced contractions decrease antigen-induced contractions, whereas lipoxygenase inhibitors reduce the contraction to A23187.
我们比较了白三烯(LT)D4受体拮抗剂FPL55712和一些脂氧合酶抑制剂,在环氧化酶抑制剂吲哚美辛(5微摩尔)存在的情况下,对由抗原(卵清蛋白,OA)和钙离子载体A23187诱导的豚鼠离体气管收缩的影响,以及对由花生四烯酸(AA)、蜂毒肽和白三烯D4(LTD4)诱导的收缩的影响。FPL55712(0.1和1微摩尔)抑制了由AA(100微摩尔)和磷脂酶A2激活剂蜂毒肽(3微克/毫升)诱导的收缩,而脂氧合酶抑制剂去甲二氢愈创木酸(NDGA,10微摩尔)对蜂毒肽反应的抑制作用比对AA反应更有效。FPL55712对由OA(100微克/毫升)诱导的收缩的抑制作用比对A23187(1微克/毫升)诱导的收缩更明显,并且在LTC4转化为LTD4的抑制剂L-丝氨酸-硼酸盐复合物(45毫摩尔)存在的情况下,FPL55712的这些抑制作用要小得多。NDGA(10微摩尔)对OA反应没有显著影响,而脂氧合酶抑制剂1-苯基-3-吡唑烷酮(非那宗,10微摩尔)和5,8,11,14-二十碳四烯酸(ETYA,10微摩尔)明显抑制了该反应。相反,NDGA和非那宗抑制了A23187反应,但ETYA对其没有影响。FPL55712、非那宗和ETYA对LTD4诱导的收缩有很大的抑制作用,但NDGA没有,并且这些抑制剂对组胺诱导的收缩没有影响。这些结果表明,在豚鼠气管中,LTD4诱导收缩的抑制剂可减少抗原诱导的收缩,而脂氧合酶抑制剂可降低对A23187的收缩反应。