Alagha Khuder, Palot Alain, Sofalvi Tunde, Pahus Laurie, Gouitaa Marion, Tummino Celine, Martinez Stephanie, Charpin Denis, Bourdin Arnaud, Chanez Pascal
Respiratory Department, AP-HM, Inserm CNRS U 1067, UMR7333, Aix Marseille Université, Marseille, France.
Respiratory Department, Arnaud de Villeneuve Hospital, Montpellier, France.
Ther Adv Chronic Dis. 2014 Mar;5(2):85-98. doi: 10.1177/2040622313518227.
Acetylcholine (neuronal and non-neuronal origin) regulates bronchoconstriction, and mucus secretion. It has an inflammatory effect by inducing attraction, survival and cytokine release from inflammatory cells. Muscarinic receptors throughout the bronchial tree are mainly restricted to muscarinic M1, M2 and M3 receptors. Three long-acting muscarinic receptor antagonists (LAMAs) were approved for the treatment of chronic obstructive pulmonary disease (COPD) in Europe: once-daily tiotropium bromide; once-daily glycopyrronium bromide; and twice-daily aclidinium bromide. All have higher selectivity for M3 receptors than for M2 receptors, and dissociate more slowly from the M3 receptors than they do from the M2 receptors. Some LAMAs showed anti-inflammatory effects [inhibition of neutrophil chemotactic activity and migration of alveolar neutrophils, decrease of several cytokines in the bronchoalveolar lavage (BAL) including interleukin (IL)-6, tumor necrosis factor (TNF)-α and leukotriene (LT)B4] and antiremodeling effects (inhibition of mucus gland hypertrophy and decrease in MUC5AC-positive goblet cell number, decrease in MUC5AC overexpression). In the clinic, LAMAs showed a significant improvement of forced expiratory volume in 1 second (FEV1), quality of life, dyspnea and reduced the number of exacerbations in COPD and more recently in asthma. This review will focus on the three LAMAs approved in Europe in the treatment of chronic airway diseases.
乙酰胆碱(源于神经元和非神经元)可调节支气管收缩和黏液分泌。它通过诱导炎症细胞的趋化、存活及细胞因子释放而产生炎症效应。整个支气管树中的毒蕈碱受体主要局限于毒蕈碱M1、M2和M3受体。三种长效毒蕈碱受体拮抗剂(LAMA)在欧洲被批准用于治疗慢性阻塞性肺疾病(COPD):每日一次的噻托溴铵;每日一次的格隆溴铵;以及每日两次的阿地溴铵。所有这些药物对M3受体的选择性均高于对M2受体,且与M3受体的解离速度比对M2受体的解离速度更慢。一些LAMA显示出抗炎作用[抑制中性粒细胞趋化活性和肺泡中性粒细胞迁移,减少支气管肺泡灌洗(BAL)中的多种细胞因子,包括白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α和白三烯(LT)B4]和抗重塑作用(抑制黏液腺肥大并减少MUC5AC阳性杯状细胞数量,降低MUC5AC过表达)。在临床上,LAMA可显著改善1秒用力呼气量(FEV1)、生活质量、呼吸困难,并减少COPD以及最近哮喘的急性加重次数。本综述将聚焦于在欧洲被批准用于治疗慢性气道疾病的三种LAMA。