Ney U M
Br J Pharmacol. 1983 Aug;79(4):1003-9. doi: 10.1111/j.1476-5381.1983.tb10548.x.
In anaesthetized, spontaneously breathing guinea-pigs, enhanced bronchoconstrictor responses (increases RL) to histamine were measured following intravenous injection of practolol, (+/-)-propranolol, (+)- and (-)-propranolol. Propranolol enhanced not only histamine- but 5-hydroxytryptamine (5-HT)-induced bronchoconstrictions and its effects lasted up to 2 h. This increased airway sensitivity was not due to beta-adrenoceptor blockade because: (a) similar effects were produced by racemic propranolol and its two isomers (+)- and (-)-propranolol and (b) whilst equal doses of (+/-)- and (+)-propranolol produced the same potentiation of histamine bronchoconstriction, only (+/-)-propranolol also caused a measurable beta-adrenoceptor blockade in the airways. The enhanced histamine- and 5-HT-induced bronchoconstrictions were antagonized by the leukotriene antagonist FPL 55712 and by the lipoxygenase/cyclo-oxygenase inhibitor BW755c. The results demonstrate that endogenously released leukotrienes can produce not only a direct bronchospasm but may enhance the effects of other bronchoconstrictor agents. The relevance of this leukotriene-mediated hyperreactivity to the non-specific airway hyperreactivity seen in asthmatics is discussed.
在麻醉状态下自主呼吸的豚鼠中,静脉注射心得宁、(±)-普萘洛尔、(+)-和(-)-普萘洛尔后,测量了对组胺增强的支气管收缩反应(气道阻力增加)。普萘洛尔不仅增强了组胺诱导的支气管收缩,还增强了5-羟色胺(5-HT)诱导的支气管收缩,其作用持续长达2小时。气道敏感性的增加并非由于β-肾上腺素受体阻断,原因如下:(a)消旋普萘洛尔及其两种异构体(+)-和(-)-普萘洛尔产生了相似的作用;(b)虽然等量的(±)-和(+)-普萘洛尔对组胺支气管收缩产生相同的增强作用,但只有(±)-普萘洛尔在气道中也引起了可测量的β-肾上腺素受体阻断。白三烯拮抗剂FPL 55712和脂氧合酶/环氧化酶抑制剂BW755c可拮抗组胺和5-HT诱导的支气管收缩增强。结果表明,内源性释放的白三烯不仅可导致直接的支气管痉挛,还可能增强其他支气管收缩剂的作用。本文讨论了这种白三烯介导的高反应性与哮喘患者中所见的非特异性气道高反应性的相关性。