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哮喘中β2肾上腺素能受体和毒蕈碱受体疗法的变化趋势

Changing face of β2-adrenergic and muscarinic receptor therapies in asthma.

作者信息

Wasilewski Nastasia V, Lougheed M Diane, Fisher John T

机构信息

Division of Respirology, Department of Medicine and Department of Biomedical & Molecular Sciences, Queen's University, Kingston, Ontario, Canada.

Division of Respirology, Department of Medicine and Department of Biomedical & Molecular Sciences, Queen's University, Kingston, Ontario, Canada.

出版信息

Curr Opin Pharmacol. 2014 Jun;16:148-56. doi: 10.1016/j.coph.2014.05.007. Epub 2014 Jun 9.

Abstract

Despite current available treatment options, a significant proportion of patients with asthma remain uncontrolled and asthma pharmacotherapy continues to evolve. β2-Adrenergic receptor agonists play a major role as bronchodilators in asthma therapy, although new perspectives reflect the potential for bias G-protein coupled receptor signaling pathways. Due to the success of muscarinic antagonists in chronic obstructive pulmonary disease, and the elucidation that muscarinic receptors play a role in airway remodeling, muscarinic receptors represent an attractive therapeutic target in asthma. Although short-acting muscarinic antagonists are currently limited to their use in acute asthma and as alternative bronchodilators in individuals who experience side effects with β2-agonists, recent clinical trials indicate that the long-acting muscarinic antagonist, tiotropium, deserves consideration as a potential therapeutic agent for select populations. The continued evolution of anticholinergic therapy in asthma will require appropriately designed studies to assess mechanisms, efficacy and safety in asthma.

摘要

尽管目前有多种治疗方案可供选择,但仍有相当一部分哮喘患者病情未得到控制,哮喘药物治疗也在不断发展。β2肾上腺素能受体激动剂作为支气管扩张剂在哮喘治疗中发挥着重要作用,尽管新的观点反映了其对G蛋白偶联受体信号通路可能存在的偏差。由于毒蕈碱拮抗剂在慢性阻塞性肺疾病治疗中取得了成功,且已明确毒蕈碱受体在气道重塑中发挥作用,因此毒蕈碱受体成为哮喘治疗中一个有吸引力的靶点。虽然短效毒蕈碱拮抗剂目前仅限于用于急性哮喘以及作为对β2激动剂有副作用的个体的替代支气管扩张剂,但最近的临床试验表明,长效毒蕈碱拮抗剂噻托溴铵值得作为特定人群的潜在治疗药物加以考虑。哮喘抗胆碱能治疗的持续发展将需要设计适当的研究来评估其在哮喘中的作用机制、疗效和安全性。

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