Ashida Y, Matsumoto T, Kuriki H, Shiraishi M, Kato K, Terao S
Biology Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.
Prostaglandins. 1989 Jul;38(1):91-112. doi: 10.1016/0090-6980(89)90019-1.
The anti-asthmatic activity of AA-2414 [(+/-)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptano ic acid] has been studied in vivo and in vitro. Experimental allergic asthma was inhibited by orally administered AA-2414 in a dose-dependent manner. AA-2414, 0.08-1.25 mg/kg (p.o.), inhibited the bronchconstriction in guinea pigs induced by a prostaglandin endoperoxide analogue (U-46619), leukotriene D4 (LTD4), and platelet activating factor (PAF) with a long duration of action. The compound did not inhibit histamine-induced bronchoconstriction. AA-2414 reduced the induction of pulmonary inflation caused by LTD4 aerosol inhalation. AA-2414 competitively inhibited the contractile response to U-46619 in guinea pig tracheal and parenchymal strips and dog saphenous vein strips with pA2 values of 7.69, 8.29 and 6.79, respectively. Furthermore, the contractile responses of guinea pig tracheal strip to PGD2, 9 alpha, 11 beta-PGF2 and PGF2 alpha were inhibited with pA2 values of 7.20, 7.79 and 5.71, respectively. These results suggest that AA-2414, a quinone derivative, is a novel, potent and orally active antagonist of a variety of spasmogenic prostanoids.
已在体内和体外研究了AA - 2414[(±)-7 - (3,5,6 - 三甲基 - 1,4 - 苯醌 - 2 - 基)-7 - 苯基庚酸]的抗哮喘活性。口服给予AA - 2414可剂量依赖性地抑制实验性过敏性哮喘。0.08 - 1.25mg/kg(口服)的AA - 2414可抑制前列腺素内过氧化物类似物(U - 46619)、白三烯D4(LTD4)和血小板活化因子(PAF)诱导的豚鼠支气管收缩,且作用持续时间长。该化合物不抑制组胺诱导的支气管收缩。AA - 2414可减少LTD4气雾剂吸入引起的肺膨胀诱导。AA - 2414竞争性抑制豚鼠气管和实质条带以及犬隐静脉条带对U - 46619的收缩反应,其pA2值分别为7.69、8.29和6.79。此外,豚鼠气管条带对PGD2、9α,11β - PGF2和PGF2α的收缩反应也受到抑制,其pA2值分别为7.20、7.79和5.71。这些结果表明,醌衍生物AA - 2414是一种新型、强效且口服活性的多种致痉挛前列腺素拮抗剂。