Division of Immunology and Allergy, Department of Chest Diseases, Erciyes University School of Medicine, Kayseri, Turkey.
J Aerosol Med Pulm Drug Deliv. 2023 Aug;36(4):189-209. doi: 10.1089/jamp.2022.0059. Epub 2023 Jul 11.
The journey of using anticholinergics in the treatment of asthma started with anticholinergic-containing plants such as Datura stramonium and Atropa belladonna, followed by ipratropium bromide and continued with tiotropium, glycopyrronium, and umeclidinium. Although antimuscarinics were used in the maintenance treatment of asthma over a century ago, after a long time (since 2014), it has been recommended to be used as an add-on long-acting antimuscarinic agent (LAMA) therapy in the maintenance treatment of asthma. The airway tone controlled by the vagus nerve is increased in asthma. Allergens, toxins, or viruses cause airway inflammation and inflammation-related epithelial damage, increased sensory nerve stimulation, ganglionic and postganglionic acetylcholine (ACh) release by inflammatory mediators, intensification of ACh signaling at M1 and M3 muscarinic ACh receptors (mAChRs), and dysfunction of M2 mAChR. Optimal anticholinergic drug for asthma should effectively block M3 and M1 receptors, but have minimal effect on M2 receptors. Tiotropium, umeclidinium, and glycopyrronium are anticholinergic agents with this feature. Tiotropium has been used in a separate inhaler as an add-on treatment to inhaled corticosteroid (ICS)/long-acting β2-agonist (LABA), and glycopyrronium and umeclidinium have been used in a single inhaler as a combination of ICS/LABA/LAMA in asthma in recent years. Guidelines recommend this regimen as an optimization step for patients with severe asthma before initiating any biologic or systemic corticosteroid therapy. In this review, the history of antimuscarinic agents, their effectiveness and safety in line with randomized controlled trials, and real-life studies in asthma treatment will be discussed according to the current data.
抗胆碱能药物在哮喘治疗中的应用历程始于含有抗胆碱能药物的植物,如曼陀罗和颠茄,随后是异丙托溴铵,接着是噻托溴铵、格隆溴铵和乌美溴铵。尽管抗毒蕈碱药物在一个多世纪前就被用于哮喘的维持治疗,但经过很长一段时间(自 2014 年以来),它才被推荐作为哮喘维持治疗的附加长效抗毒蕈碱药物(LAMA)治疗。迷走神经控制的气道张力在哮喘中增加。过敏原、毒素或病毒引起气道炎症和炎症相关的上皮损伤,增加感觉神经刺激,炎症介质引起的神经节和节后乙酰胆碱(ACh)释放,M1 和 M3 毒蕈碱 ACh 受体(mAChR)的 ACh 信号增强,以及 M2 mAChR 功能障碍。哮喘的最佳抗胆碱能药物应该能够有效阻断 M3 和 M1 受体,但对 M2 受体的影响最小。噻托溴铵、乌美溴铵和格隆溴铵具有这种特性。噻托溴铵已作为附加治疗药物与吸入皮质类固醇(ICS)/长效β2-激动剂(LABA)联合使用于单独的吸入器中,近年来,格隆溴铵和乌美溴铵已在单一吸入器中与 ICS/LABA/LAMA 联合用于哮喘治疗。指南建议,在开始任何生物制剂或全身皮质类固醇治疗之前,将这种方案作为重度哮喘患者的优化步骤。在本综述中,根据当前数据,将讨论抗毒蕈碱药物的历史、在随机对照试验中的有效性和安全性,以及在哮喘治疗中的真实世界研究。