Drazen J M, Austen K F, Lewis R A, Clark D A, Goto G, Marfat A, Corey E J
Proc Natl Acad Sci U S A. 1980 Jul;77(7):4354-8. doi: 10.1073/pnas.77.7.4354.
The pharmacologic activities of leukotrienes C-1 and D(LTC-1 and LTD), constituents of slow reacting substance of anaphylaxis (SRS-A), were evaluated in vitro on airway contractile tissues and in vivo on pulmonary mechanical function, mean systemic arterial pressure, and cutaneous microcirculation. In vitro both LTC-1 and LTD were potent and selective peripheral airway agonists, being more active than histamine; furthermore, LTD was active on peripheral airways at concentrations 1/100th those of LTC-1. The concentration-effect relationship for LTD and the profile of antagonism by FPL 55712 are consistent with the activity of this molecule at two separate peripheral airway receptors. In vivo, LTC-1 and LTD were nearly equally active in their effects on pulmonary mechanics, and the pattern of alterations was consistent with the predominant site of action being in the lung periphery. Furthermore, both agents had a direct systemic arterial hypotensive effect and were vasoactive on the cutaneous microcirculation. Thus, these compounds are likely to be major mediators of the pathologic alterations in immediate type hypersensitivity reactions in which peripheral airway constriction and hypotension are prominent features.
对过敏反应慢反应物质(SRS-A)的成分白三烯C-1和D(LTC-1和LTD)的药理活性进行了体外气道收缩组织评估以及体内肺机械功能、平均体动脉压和皮肤微循环评估。在体外,LTC-1和LTD都是强效且选择性的外周气道激动剂,比组胺更具活性;此外,LTD在外周气道上的活性浓度是LTC-1的1/100。LTD的浓度-效应关系以及FPL 55712的拮抗作用特征与该分子在两个不同外周气道受体上的活性一致。在体内,LTC-1和LTD对肺机械功能的影响几乎同样活跃,且改变模式与主要作用部位在肺外周一致。此外,两种药物都有直接的体动脉降压作用,并且对皮肤微循环有血管活性作用。因此,这些化合物可能是速发型超敏反应中病理改变的主要介质,其中外周气道收缩和低血压是突出特征。