Negro J M, Miralles J C, Ortiz J L, Funes E, García A
Allergology Section, H.U. Virgen de la Arrixaca, El Palmar, Murcia, Spain.
Allergol Immunopathol (Madr). 1997 Mar-Apr;25(2):104-12.
Cysteinyl leukotrienes are important mediators of asthma, and inhibition of their effects may represent a potential breakthrough in the therapy of allergic rhinitis and asthma. Strategies for inhibition of cysteinyl leukotriene receptors and inhibition of 5-lipoxygenase activity. The leukotrienes antagonists, with particular reference to asthma and allergic rhinitis, is reviewed in this paper. In studies in asthmatic patients, these compounds can inhibit bronchoconstriction in response to exercise, aspirin and allergen. Results from clinical studies using receptor antagonists, such as LY-171883, SK&F-104353, ICI-204219, ONO-1078, MK-751, MK-0679, demonstrate beneficial effects, with improvement in symptoms and forced expiratory volume in one second (FEV1), and a reduction in the use of beta 2-adrenergic relief medication. NZ-107 was studied for its effect on airway inflammation caused by intratracheal injection of LTB4 or IL-5, or by inhalation of PAF, and by cell activation. Analysis of the BAL fluid revealed that both induced eosinophilia and neutrophilia were suppressed. Surprisingly, although PAF and superoxide generation were inhibited in macrophages and eosinophils, NZ-107 had no effect on neutrophil activation. U-75302 was studied in guinea pigs and inhibited LTB4 induced chemotaxis of eosinophils in vitro and antigen-induced lung eosinophilia in vivo. Further studies are needed to clarify the exact mechanism by which these compounds provide beneficial effects.
半胱氨酰白三烯是哮喘的重要介质,抑制其作用可能代表着变应性鼻炎和哮喘治疗方面的潜在突破。抑制半胱氨酰白三烯受体和抑制5-脂氧合酶活性的策略。本文综述了白三烯拮抗剂,特别是针对哮喘和变应性鼻炎的相关内容。在哮喘患者的研究中,这些化合物可抑制运动、阿司匹林和变应原引起的支气管收缩。使用受体拮抗剂(如LY-171883、SK&F-104353、ICI-204219、ONO-1078、MK-751、MK-0679)的临床研究结果显示出有益效果,症状得到改善,一秒用力呼气量(FEV1)增加,β2-肾上腺素能缓解药物的使用减少。研究了NZ-107对气管内注射LTB4或IL-5、吸入PAF以及细胞活化所引起的气道炎症的影响。对支气管肺泡灌洗(BAL)液的分析表明,诱导的嗜酸性粒细胞增多和中性粒细胞增多均受到抑制。令人惊讶的是,尽管PAF和超氧化物生成在巨噬细胞和嗜酸性粒细胞中受到抑制,但NZ-107对中性粒细胞活化没有影响。在豚鼠中研究了U-75302,它在体外抑制LTB4诱导的嗜酸性粒细胞趋化作用,在体内抑制抗原诱导的肺嗜酸性粒细胞增多。需要进一步研究以阐明这些化合物产生有益效果的确切机制。