Abstract
Introduction: Asthma and chronic obstructive pulmonary disease (COPD) are inflammatory disorders that have an increasing prevalence and associated morbidity and mortality. βÎ2-adrenoceptor agonists (βÎ2-agonists) act by stimulating the βÎ2-adrenoceptor present on airway smooth muscle and other cells in the airway, resulting in bronchodilatation. βÎ2-agonists are among the most commonly used drugs in the world and remain pivotal in the treatment of symptoms in patients with asthma and COPD. Salbutamol is a chiral drug with (R)-and (S)-isomers. Almost all βÎ2-agonists that are used at present are racemic mixtures of (R)-and (S)-salbutamol. Areas covered: In this review the authors show that (R)-salbutamol alone (generically known as levosalbutamol) provides beneficial βÎ2-agonist effects at a cellular level and in experimental models of airways disease. In addition the authors demonstrate that (S)-salbutamol opposes the desirable effects of (R)-salbutamol and can actually cause features of asthma and COPD in vitro and in experimental asthma. Expert opinion: Despite this strong body of experimental evidence, (R)-salbutamol has not shown consistent superiority over (S)-or racemic salbutamol in human asthma or COPD.
Original language | English |
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Pages (from-to) | 1133-1141 |
Number of pages | 9 |
Journal | Expert Opinion on Pharmacotherapy |
Volume | 12 |
Issue number | 7 |
DOIs | |
Publication status | Published - 1 Apr 2011 |
Keywords
- (R)-salbutamol
- (S)-salbutamol
- asthma
- b2-agonist
- chronic obstructive pulmonary disease (COPD)
- levosalbutamol