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SK&F 104353,一种选择性白三烯受体拮抗剂,可抑制食蟹猴中白三烯D4和抗原诱导的支气管收缩。

SK&F 104353, a selective leukotriene receptor antagonist, inhibits leukotriene D4- and antigen-induced bronchoconstriction in cynomolgus monkeys.

作者信息

Osborn R R, Hay D W, Wasserman M A, Torphy T J

机构信息

Department of Pharmacology, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406-0939.

出版信息

Pulm Pharmacol. 1992 Sep;5(3):153-7. doi: 10.1016/0952-0600(92)90035-f.

Abstract

The ability of SK&F 104353 to prevent and reverse leukotriene (LT) D4- and antigen (Ag)-induced bronchoconstriction was examined in anesthetized, spontaneously breathing cynomolgus monkeys. Aerosol administration of LTD4 (10 micrograms/ml; 20 breaths) produced a sustained increase in pulmonary resistance and decrease in dynamic lung compliance. Aerosolized SK&F 104353 (150 breaths, 0.3 or 4.4 mg/ml) administered 15 min prior to LTD4 challenge antagonized these changes in a dose-dependent manner. When given intravenously 6 min after LTD4, SK&F 104353 (5 mg/kg) rapidly and completely reversed the ongoing bronchoconstriction. In mepyramine-pretreated (2 mg/kg i.v.) monkeys sensitive to aerosolized Ascaris suum Ag, intravenously administered SK&F 104353 (5 mg/kg) substantially reversed, but did not abolish, Ag-induced bronchoconstriction when administered 12 min after the Ag challenge. In contrast, SK&F 104353 (5 mg/kg i.v.) did not reverse Ag-induced bronchoconstriction in animals that had not been pretreated with mepyramine. Similar results were obtained when SK&F 104353 (20 mg/kg i.v.) was administered (as a pretreatment) 5 min prior to Ag under these conditions. Thus, SK&F 104353 reduced Ag-induced bronchoconstriction in mepyramine-pretreated monkeys, but had little effect in the absence of mepyramine. The data suggest that LTs, in addition to histamine, play a role in allergic bronchoconstriction in cynomolgus monkeys.

摘要

在麻醉状态下自主呼吸的食蟹猴中,研究了SK&F 104353预防和逆转白三烯(LT)D4及抗原(Ag)诱导的支气管收缩的能力。雾化吸入LTD4(10微克/毫升;20次呼吸)可使肺阻力持续增加,动态肺顺应性降低。在LTD4激发前15分钟雾化吸入SK&F 104353(150次呼吸,0.3或4.4毫克/毫升),可剂量依赖性地拮抗这些变化。在LTD4给药6分钟后静脉注射SK&F 104353(5毫克/千克),可迅速且完全逆转正在进行的支气管收缩。在对雾化猪蛔虫抗原敏感且经美吡拉敏预处理(静脉注射2毫克/千克)的猴子中,静脉注射SK&F 104353(5毫克/千克),在抗原激发后12分钟给药,可显著逆转但不能消除抗原诱导的支气管收缩。相比之下,在未用美吡拉敏预处理的动物中,SK&F 104353(静脉注射5毫克/千克)不能逆转抗原诱导的支气管收缩。在这些条件下,当在抗原激发前5分钟静脉注射SK&F 104353(20毫克/千克)(作为预处理)时,也得到了类似结果。因此,SK&F 104353可减轻经美吡拉敏预处理的猴子中抗原诱导的支气管收缩,但在没有美吡拉敏时作用很小。数据表明,白三烯除组胺外,在食蟹猴的过敏性支气管收缩中起作用。

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