Frey H H, Dengjel C
Eur J Pharmacol. 1976 Dec;40(2):345-8. doi: 10.1016/0014-2999(76)90072-8.
In cats, anesthetized with chloralose, vagotomized and relaxed by infusion of sexamethonium, bronchoconstrictor reactions were induced by the i.v. injection of arachidonic acid (50 to 200 mug/kg). These reactions could be completely suppressed by the following drugs: indomethacin (ED50 0.16 mg/kg), flufenamic acid (1.8 mg/kg), acetylsalicylic acid (2.4 mg/kg) and phenylbutazone (4.7 mg/kg), but paracetamol was only partly effective even in doses up to 50 mg/kg. The results show that rather small doses of most weak analgesics can effectively inhibit prostaglandin biosynthesis in the bronchi and make it likely that this inhibition is involved in the drug-induced bronchoconstrictor reactions, which have been observed clinically.
在使用水合氯醛麻醉、切断迷走神经并通过注入氯琥珀胆碱使其松弛的猫中,静脉注射花生四烯酸(50至200微克/千克)可诱发支气管收缩反应。以下药物可完全抑制这些反应:吲哚美辛(半数有效量0.16毫克/千克)、氟芬那酸(1.8毫克/千克)、乙酰水杨酸(2.4毫克/千克)和保泰松(4.7毫克/千克),但对乙酰氨基酚即使剂量高达50毫克/千克也只是部分有效。结果表明,大多数弱镇痛药的相当小剂量就能有效抑制支气管中的前列腺素生物合成,并使得这种抑制作用可能与临床上观察到的药物诱发的支气管收缩反应有关。