Dale Philippa R, Cernecka Hana, Schmidt Martina, Dowling Mark R, Charlton Steven J, Pieper Michael P, Michel Martin C
Department of Pharmacology, Cambridge University, Cambridge, UK.
University of Groningen, Department of Molecular Pharmacology, Groningen, The Netherlands; University of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD, GRIAC, Groningen, The Netherlands.
Curr Opin Pharmacol. 2014 Jun;16(100):31-42. doi: 10.1016/j.coph.2014.03.003. Epub 2014 Mar 27.
Muscarinic receptor antagonists and β-adrenoceptor agonists are used in the treatment of obstructive airway disease and overactive bladder syndrome. Here we review the pharmacological rationale for their combination. Muscarinic receptors and β-adrenoceptors are physiological antagonists for smooth muscle tone in airways and bladder. Muscarinic agonism may attenuate β-adrenoceptor-mediated relaxation more than other contractile stimuli. Chronic treatment with one drug class may regulate expression of the target receptor but also that of the opposing receptor. Prejunctional β2-adrenoceptors can enhance neuronal acetylcholine release. Moreover, at least in the airways, muscarinic receptors and β-adrenoceptors are expressed in different locations, indicating that only a combined modulation of both systems may cause dilatation along the entire bronchial tree. While all of these factors contribute to a rationale for a combination of muscarinic receptor antagonists and β-adrenoceptor agonists, the full value of such combination as compared to monotherapy can only be determined in clinical studies.
毒蕈碱受体拮抗剂和β-肾上腺素能受体激动剂用于治疗阻塞性气道疾病和膀胱过度活动症。在此,我们综述它们联合使用的药理学原理。毒蕈碱受体和β-肾上腺素能受体是气道和膀胱平滑肌张力的生理性拮抗剂。与其他收缩刺激相比,毒蕈碱激动作用可能更能减弱β-肾上腺素能受体介导的舒张作用。长期使用一类药物治疗可能会调节靶受体的表达,但也会调节其拮抗受体的表达。突触前β2-肾上腺素能受体可增强神经元乙酰胆碱释放。此外,至少在气道中,毒蕈碱受体和β-肾上腺素能受体在不同位置表达,这表明只有对这两个系统进行联合调节才可能使整个支气管树扩张。虽然所有这些因素都为毒蕈碱受体拮抗剂和β-肾上腺素能受体激动剂联合使用提供了理论依据,但与单一疗法相比,这种联合疗法的全部价值只能在临床研究中确定。