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咳嗽、哮喘和半胱氨酰白三烯。

Cough, asthma, and cysteinyl-leukotrienes.

机构信息

Dept of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

出版信息

Pulm Pharmacol Ther. 2013 Oct;26(5):514-9. doi: 10.1016/j.pupt.2013.06.003. Epub 2013 Jun 15.

Abstract

Asthma is a chronic inflammatory disease of the lower airways, involving various cells such as eosinophils, and cytokines and mediators. Cyteinyl-leukotrienes (cys-LTs) are one of the chemical mediators that play major pathophysiological roles in asthma. They are produced by eosinophils and mast cells, and induce bronchoconstriction, mucous hypersecretion, microvascular leakage, eosinophil chemotaxis and airway remodeling. Anti-leukotrienes, including leukotriene receptor antagonists (LTRAs) which block cysLT1 receptors, exert both bronchodilatory and anti-inflammatory effects and are utilized as second- to third-line controller medication of persistent asthma. Cough is a major symptom of asthma, and cough variant asthma (CVA) is an asthma phenotype that solely presents with coughing. Sputum levels of cys-LTs are increased in patients with CVA. Antitussive effects of monotherapy with LTRAs in patients with CVA have been reported. We have recently demonstrated that 4 weeks' treatment with an LTRA montelukast exerted anti-inflammatory effect as proved by a decrease of sputum eosinophils, in addition to attenuation of cough VAS and capsaicin cough sensitivity, as reported previously. Spirometry, airway responsiveness, and impulse oscillation indices (respiratory resistance and reactance) were unchanged. These results suggested that the antitussive effect of montelukast in CVA might be attributable to its anti-inflammatory ability rather than bronchodilation. The treatment did not affect sputum levels of mediators (cys-LTs, LTB4, PGD2, PGE2, PGF2α, and TXB2). Since inhaled corticosteroid does not seem to affect cough sensitivity while attenuating cough in patients with CVA, LTRAs may involve different mechanism(s) from that of corticosteroid. LTRAs must theoretically be effective against cough of asthmatic subjects through its "anti-asthma" effects, while evidence supporting direct antitussive effects of cys-LTs on "cough receptors" is scarce. An important clinical question is that whether LTRAs involve non-specific antitussive effects. While a definite answer is not available yet, this possibility seems unlikely at the moment, although some secondary anti-inflammatory properties have been reported for montelukast. This issue needs to be clarified by future research to avoid overuse of this expensive class of medication.

摘要

哮喘是一种慢性气道炎症性疾病,涉及多种细胞,如嗜酸性粒细胞和细胞因子及介质。半胱氨酰白三烯(cysteinyl-leukotrienes,cys-LTs)是在哮喘中发挥主要病理生理作用的化学介质之一。它们由嗜酸性粒细胞和肥大细胞产生,可引起支气管收缩、黏液过度分泌、微血管渗漏、嗜酸性粒细胞趋化和气道重塑。抗白三烯药物,包括阻断 cysLT1 受体的白三烯受体拮抗剂(leukotriene receptor antagonists,LTRAs),具有支气管扩张和抗炎作用,可用作持续性哮喘的二线至三线控制药物。咳嗽是哮喘的主要症状,咳嗽变异性哮喘(cough variant asthma,CVA)是一种仅表现为咳嗽的哮喘表型。CVA 患者的 cys-LTs 水平升高。报道称,LTRA 单药治疗 CVA 具有镇咳作用。我们最近的研究表明,4 周的 LTRA 孟鲁司特治疗除了以前报道的咳嗽视觉模拟量表(VAS)和辣椒素咳嗽敏感性降低外,还具有抗炎作用,表现为痰中嗜酸性粒细胞减少。肺量计、气道反应性和脉冲振荡指数(呼吸阻力和电抗)没有变化。这些结果表明,孟鲁司特治疗 CVA 的镇咳作用可能归因于其抗炎能力而不是支气管扩张作用。该治疗方法不影响介质(cys-LTs、LTB4、PGD2、PGE2、PGF2α 和 TXB2)的痰液水平。由于吸入皮质类固醇似乎不会影响 CVA 患者的咳嗽敏感性,同时减轻咳嗽,LTRAs 可能与皮质类固醇的作用机制不同。LTRAs 理论上应该通过其“抗哮喘”作用对哮喘患者的咳嗽有效,而关于 cys-LTs 对“咳嗽受体”的直接镇咳作用的证据很少。一个重要的临床问题是 LTRAs 是否涉及非特异性镇咳作用。虽然目前还没有明确的答案,但这种可能性似乎不太可能,尽管已经报道了孟鲁司特的一些次要抗炎特性。这个问题需要通过未来的研究来澄清,以避免过度使用这种昂贵的药物类别。

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