Boot J R, Bond A, Thomas K H, O'Brien A, Gilmore J, Todd A
Eli Lilly & Co., Lilly Research Centre Ltd., Windlesham, Surrey, UK.
Eur J Pharmacol. 1993 Jan 26;231(1):83-9. doi: 10.1016/0014-2999(93)90687-d.
This study describes the evaluation of LY290324 as a leukotriene D4 (LTD4) receptor antagonist in guinea-pigs. In vitro, LY290324 was a potent and persistent antagonist of the contractile responses to LTD4 and LTE4 with pA2 values of 9.1 +/- 0.2 and 8.9 +/- 0.17 respectively. The antagonism appeared competitive and selective for LTD4/E4, as LY290324 (10(-6) M) had no effects on contraction elicited by LTC4, prostaglandin F2 alpha (PGF2 alpha), histamine and acetylcholine. In vivo the compound was highly effective in a dose-dependent manner by the intravenous, oral and inhaled routes in preventing LTD4-induced bronchospasm. Administered i.v. LY290324 prevented the development (ED50 = 3.4 micrograms/kg) of an LTD4-induced bronchospasm and readily reversed an established bronchospasm, but failed to prevent the bronchospasm to either histamine or platelet activating factor (PAF). Oral studies demonstrated efficacy for at least 12 h. Administered orally 6 h previously, LY290324 reduced LTC4, LTD4 and LTE4-induced bronchospasm with ED50s of 0.3, 0.28 and 0.37 mg/kg respectively. Relatively low inhaled levels (2 micrograms/kg) also significantly reduced (72.5%, P < 0.001) LTD4-induced bronchospasm. Finally the compound administered orally was effective in reducing antigen-induced bronchospasm in immunologically sensitised animals.
本研究描述了LY290324作为豚鼠白三烯D4(LTD4)受体拮抗剂的评估情况。在体外,LY290324是对LTD4和LTE4收缩反应的强效且持久的拮抗剂,其pA2值分别为9.1±0.2和8.9±0.17。这种拮抗作用对LTD4/E4表现出竞争性和选择性,因为LY290324(10⁻⁶ M)对LTC4、前列腺素F2α(PGF2α)、组胺和乙酰胆碱引起的收缩无影响。在体内,该化合物通过静脉、口服和吸入途径以剂量依赖方式高度有效地预防LTD4诱导的支气管痉挛。静脉注射LY290324可预防LTD4诱导的支气管痉挛的发生(ED50 = 3.4微克/千克),并能迅速逆转已形成的支气管痉挛,但不能预防组胺或血小板活化因子(PAF)引起的支气管痉挛。口服研究表明其疗效至少持续12小时。提前6小时口服LY290324可减轻LTC4、LTD4和LTE4诱导的支气管痉挛,其ED50分别为0.3、0.28和0.37毫克/千克。相对较低的吸入水平(2微克/千克)也能显著减轻(72.5%,P < 0.001)LTD4诱导的支气管痉挛。最后,口服该化合物可有效减轻免疫致敏动物中抗原诱导的支气管痉挛。