McMillan R M
AstraZeneca, Mereside, Alderley Park, Macclesfield, SK, 10 4TG, UK.
Paediatr Respir Rev. 2001 Sep;2(3):238-44. doi: 10.1053/prrv.2001.0146.
Arachidonic acid metabolism via 5-lipoxygenase gives rise to a group of biologically active lipids known as leukotrienes: leukotriene B(4), which is a potent activator of leukocyte chemotaxis, and cysteinyl leukotrienes (leukotriene C(4), D(4)and E(4)) which account for the spasmogenic activity previously described as slow-reacting substance of anaphylaxis. The biological actions of leukotrienes and the observations that leukotrienes are synthesised in the lung following antigen provocation and are elevated in asthma, stimulated considerable activity in the pharmaceutical industry to find drugs that modulate the synthesis or actions of leukotrienes. Three cysteinyl leukotriene antagonists (zafirlukast [Accolate], montelukast [Singulair] and pranlukast) and one 5-lipoxygenase inhibitor (zileuton) have received regulatory approval for the treatment of asthma. The clinical data obtained from using these drugs are generally consistent and complimentary. As a class the leukotriene modulators produce a rapid improvement in lung function after the first oral dose. Lung function improvements are maintained on chronic administration and are associated with reductions in a variety of asthma symptom scores. All of the available data are consistent with the hypothesis that all the leukotriene modulators exert their clinical benefit primarily through interference with cysteinyl leukotrienes. There are no compelling clinical data for an additional contribution by leukotriene B(4)in human asthma. In other respiratory conditions such as COPD, which are characterised by pronounced neutrophil infiltration, it may be that the chemotactic properties of leukotriene B(4)are more important and therefore evaluation of 5-lipoxygenase inhibitors in this condition is warranted. The introduction of the leukotriene modulators into clinical practice is the culmination of over 60 years of research since the initial discovery of the slow-reacting substances. The leukotriene modulators, and in particular the cysteinyl leukotriene antagonists, provide respiratory physicians with an oral therapeutic option and have set an efficacy standard which new oral anti-inflammatory approaches will have to beat.
花生四烯酸通过5-脂氧合酶代谢产生一组被称为白三烯的生物活性脂质:白三烯B4,它是白细胞趋化性的有效激活剂;以及半胱氨酰白三烯(白三烯C4、D4和E4),它们导致了先前被描述为过敏反应慢反应物质的致痉挛活性。白三烯的生物学作用以及白三烯在抗原激发后在肺部合成且在哮喘中升高的观察结果,激发了制药行业的大量研究活动,以寻找调节白三烯合成或作用的药物。三种半胱氨酰白三烯拮抗剂(扎鲁司特[安可来]、孟鲁司特[顺尔宁]和普仑司特)以及一种5-脂氧合酶抑制剂(齐留通)已获得治疗哮喘的监管批准。使用这些药物获得的临床数据总体上是一致且互补的。作为一类药物,白三烯调节剂在首次口服给药后能迅速改善肺功能。长期给药可维持肺功能改善,并伴有多种哮喘症状评分的降低。所有现有数据都与以下假设一致,即所有白三烯调节剂主要通过干扰半胱氨酰白三烯发挥临床益处。在人类哮喘中,没有令人信服的临床数据表明白三烯B4有额外作用。在其他以明显中性粒细胞浸润为特征的呼吸道疾病如慢性阻塞性肺疾病中,白三烯B4的趋化特性可能更重要,因此有必要在此类疾病中评估5-脂氧合酶抑制剂。自最初发现慢反应物质以来,经过60多年的研究,白三烯调节剂才引入临床实践。白三烯调节剂,尤其是半胱氨酰白三烯拮抗剂,为呼吸内科医生提供了一种口服治疗选择,并设定了新的口服抗炎方法必须超越的疗效标准。