Department of Pharmaceutical Sciences, Lloyd L. Gregory School of Pharmacy, Palm Beach Atlantic University, West Palm Beach, FL 33416, USA.
Department of Molecular Pharmacology, University of Groningen, 9713 AV Groningen, The Netherlands.
Cells. 2021 May 18;10(5):1237. doi: 10.3390/cells10051237.
Expression of bronchodilatory β-adrenoceptors and bronchoconstrictive muscarinic M-receptors alter with airway size. In COPD, (a combination of) β-agonists and muscarinic M-antagonists (anticholinergics) are used as bronchodilators. We studied whether differential receptor expression in large and small airways affects the response to β-agonists and anticholinergics in COPD. Bronchoprotection by indacaterol (β-agonist) and glycopyrrolate (anticholinergic) against methacholine- and EFS-induced constrictions of large and small airways was measured in guinea pig and human lung slices using video-assisted microscopy. In guinea pig lung slices, glycopyrrolate (1, 3 and 10 nM) concentration-dependently protected against methacholine- and EFS-induced constrictions, with no differences between large and small intrapulmonary airways. Indacaterol (0.01, 0.1, 1 and 10 μM) also provided concentration-dependent protection, which was greater in large airways against methacholine and in small airways against EFS. Indacaterol (10 μM) and glycopyrrolate (10 nM) normalized small airway hyperresponsiveness in COPD lung slices. Synergy of low indacaterol (10 nM) and glycopyrrolate (1 nM) concentrations was greater in LPS-challenged guinea pigs (COPD model) compared to saline-challenged controls. In conclusion, glycopyrrolate similarly protects large and small airways, whereas the protective effect of indacaterol in the small, but not the large, airways depends on the contractile stimulus used. Moreover, findings in a guinea pig model indicate that the synergistic bronchoprotective effect of indacaterol and glycopyrrolate is enhanced in COPD.
气道大小改变了支气管扩张β-肾上腺素能受体和支气管收缩性毒蕈碱 M 受体的表达。在 COPD 中,β-激动剂和毒蕈碱 M 拮抗剂(抗胆碱能药物)被用作支气管扩张剂。我们研究了大气道和小气道中差异表达的受体是否会影响 COPD 患者对β-激动剂和抗胆碱能药物的反应。使用视频辅助显微镜,在豚鼠和人肺切片中研究了吲达特罗(β-激动剂)和格隆溴铵(抗胆碱能药物)对乙酰甲胆碱和 EFS 诱导的大气道和小气道收缩的支气管保护作用。在豚鼠肺切片中,格隆溴铵(1、3 和 10 nM)浓度依赖性地保护乙酰甲胆碱和 EFS 诱导的收缩,大气道和小气道之间没有差异。吲达特罗(0.01、0.1、1 和 10 μM)也提供了浓度依赖性的保护,对乙酰甲胆碱的大气道和对 EFS 的小气道更大。吲达特罗(10 μM)和格隆溴铵(10 nM)使 COPD 肺切片的小气道高反应性正常化。在 LPS 挑战的豚鼠(COPD 模型)中,低浓度吲达特罗(10 nM)和格隆溴铵(1 nM)的协同作用大于盐水挑战的对照组。总之,格隆溴铵相似地保护大气道和小气道,而吲达特罗在小气道中的保护作用(但不是大气道)取决于所使用的收缩刺激。此外,豚鼠模型中的研究结果表明,吲达特罗和格隆溴铵的协同支气管保护作用在 COPD 中增强。