Asthma and COPD: A Focus on β-Agonists - Past, Present and Future.
Autor: | Baker JG; Department of Respiratory Medicine, Queen's Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, UK. Jillian.Baker@nottingham.ac.uk.; Cell Signalling, Medical School, Queen's Medical Centre, University of Nottingham, Nottingham, UK. Jillian.Baker@nottingham.ac.uk., Shaw DE; Nottingham NIHR Respiratory Biomedical Research Centre, University of Nottingham, Nottingham, UK. |
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Jazyk: | angličtina |
Zdroj: | Handbook of experimental pharmacology [Handb Exp Pharmacol] 2024; Vol. 285, pp. 369-451. |
DOI: | 10.1007/164_2023_679 |
Abstrakt: | Asthma has been recognised as a respiratory disorder for millennia and the focus of targeted drug development for the last 120 years. Asthma is one of the most common chronic non-communicable diseases worldwide. Chronic obstructive pulmonary disease (COPD), a leading cause of morbidity and mortality worldwide, is caused by exposure to tobacco smoke and other noxious particles and exerts a substantial economic and social burden. This chapter reviews the development of the treatments of asthma and COPD particularly focussing on the β-agonists, from the isolation of adrenaline, through the development of generations of short- and long-acting β-agonists. It reviews asthma death epidemics, considers the intrinsic efficacy of clinical compounds, and charts the improvement in selectivity and duration of action that has led to our current medications. Important β2-agonist compounds no longer used are considered, including some with additional properties, and how the different pharmacological properties of current β2-agonists underpin their different places in treatment guidelines. Finally, it concludes with a look forward to future developments that could improve the β-agonists still further, including extending their availability to areas of the world with less readily accessible healthcare. (© 2023. The Author(s), under exclusive license to Springer Nature Switzerland AG.) |
Databáze: | MEDLINE |
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