Nicosia S
Institute of Pharmacological Sciences, Milan, Italy.
Monaldi Arch Chest Dis. 1999 Jun;54(3):242-6.
Leukotrienes (LTs) are among the most important mediators of asthma; cysteine-containing LTs (cysteinyl-LTs, i.e. LTC4, LTD4 and LTE4) are very potent bronchoconstrictors and participate in the inflammatory component of asthma by inducing mucus hypersecretion, plasma extravasation, mucosal oedema and eosinophil recruitment. Therefore, compounds able to inhibit either the formation or the action of LTs are potential antiasthma drugs and, at present, the cysteinyl-LT receptor antagonists (LTRAs) appear to be the most promising. The receptors for cysteinyl-LTs, termed CysLT receptors, are heterogeneous; at least two different classes have so far been recognized, named CysLT1 (blocked by the so-called classical antagonists, such as FPL 55712, ICI 198,615, ICI 204,219, SK&F 104353, MK-476 and others) and CysLT2 (insensitive to the classical antagonists, but sensitive to BAY u9773). The authors' results indicate that even more receptor subclasses might exist in human airways, which discriminate between LTC4 and LTD4, both asthma mediators. Among the many LTRAs, zafirlukast (Accolate, ICI 204,219), montelukast (Singulair, MK-476) and pranlukast (Onon, ONO-1078) are available for clinical use. All the LTRAs are able to inhibit LTD4-induced bronchoconstriction in humans, albeit with different potencies. With respect to antigen challenge, all of them inhibit the early phase of response, whereas only the most recently developed and potent ones are effective in the late phase. LTRAs are effective in asthma triggered by exercise, cold or aspirin. Furthermore, although they are not bronchodilators per se, they increase basal forced expiratory volume in one second in patients with mild-to-moderate asthma, indicating that, in these individuals, constant cysteinyl-LT release contributes to maintaining increased bronchial tone. Finally, the effect of LTRAs is additive to that of beta-agonists and is potentiated by antihistamine compounds. In conclusion, the available results clearly indicate that leukotrienes play an important role in asthma and that cysteinyl leukotriene receptor antagonists are very promising antiasthma drugs.
白三烯(LTs)是哮喘最重要的介质之一;含半胱氨酸的白三烯(半胱氨酰白三烯,即LTC4、LTD4和LTE4)是非常强效的支气管收缩剂,通过诱导黏液分泌过多、血浆渗出、黏膜水肿和嗜酸性粒细胞募集参与哮喘的炎症成分。因此,能够抑制白三烯形成或作用的化合物是潜在的抗哮喘药物,目前,半胱氨酰白三烯受体拮抗剂(LTRAs)似乎最有前景。半胱氨酰白三烯的受体,称为半胱氨酰白三烯受体,是异质性的;到目前为止至少已识别出两种不同类型,命名为CysLT1(被所谓的经典拮抗剂阻断,如FPL 55712、ICI 198,615、ICI 204,219、SK&F 104353、MK-476等)和CysLT2(对经典拮抗剂不敏感,但对BAY u9773敏感)。作者的结果表明,人类气道中可能存在更多的受体亚类,它们能够区分LTC4和LTD4这两种哮喘介质。在众多的LTRAs中,扎鲁司特(Accolate,ICI 204,219)、孟鲁司特(顺尔宁,MK-476)和普仑司特(Onon,ONO-1078)可用于临床。所有的LTRAs都能够抑制人类中LTD4诱导的支气管收缩,尽管效力不同。对于抗原激发,它们都能抑制反应的早期阶段,而只有最新开发且效力最强的LTRAs在晚期阶段有效。LTRAs对运动、寒冷或阿司匹林引发的哮喘有效。此外,尽管它们本身不是支气管扩张剂,但它们能增加轻至中度哮喘患者的基础一秒用力呼气量,这表明在这些个体中,持续的半胱氨酰白三烯释放有助于维持支气管张力增加。最后,LTRAs的作用与β-激动剂的作用相加,并被抗组胺化合物增强。总之,现有结果清楚地表明白三烯在哮喘中起重要作用,并且半胱氨酰白三烯受体拮抗剂是非常有前景的抗哮喘药物。