Effects of long-acting and short-acting beta-agonists on methacholine dose-response curves in asthmatics

Regular use of short-acting beta-agonists may decrease control of asthma and increase airway responsiveness to bronchoconstrictor stimuli. The aim of this study was to determine the effects of regular treatment with the long-acting beta-agonist, salmeterol, on the methacholine dose-response curve (DRC) in mild-to-moderate asthmatics. Changes in methacholine airway responsiveness were measured in 14 stable adult asthmatics, randomized in a double-blind, three-way cross-over design to receive salmeterol 50 micrograms, salbutamol 200 micrograms or placebo, each twice daily for 4 days. Two baseline methacholine DRC, were performed, one without premedication and one following a single dose of 200 micrograms salbutamol. Following 4 days of regular treatment, methacholine DRC to plateau were carried out commencing 15 min after the final dose of trial medication. There were no significant differences in mean baseline forced expiratory volume in one second (FEV1) between treatments. Four days treatment with salmeterol and salbutamol shifted the DRC to the right, but salmeterol provided less protection than salbutamol. The point of inflection of the curve from baseline moved 1.9 and 3.2 doubling doses, respectively, compared to placebo (p < or = 0.001), and the provocative concentration of methacholine required to produce a 20% fall in FEV1 (PC20) increased 1.6 and 3.1 doubling doses, respectively (p < or = 0.001). The slope of the DRC was increased slightly by both beta-agonists compared to placebo (log slope 3.11, 3.06 and 2.77 for salmeterol, salbutamol and placebo, respectively). This effect of regular salmeterol on slope was more marked in subjects with lower baseline FEV1. Maximal response plateaus did not differ between the three treatments. These results suggest that regular use either of short- or long-acting beta-agonists could increase the risk of a more precipitous asthma episode associated with "breakthrough" bronchoconstrictor responses, particularly in those with more severe initial airflow obstruction, if subjects are exposed to a sufficiently potent stimulus.

This article has been cited by other articles:

				M. A. Giembycz and R. Newton Beyond the dogma: novel {beta}2-adrenoceptor signalling in the airways. Eur. Respir. J., June 1, 2006; 27(6): 1286 - 1306. [Abstract] [Full Text] [PDF]

				L. Prieto, V. Gutierrez, V. Torres, S. Uixera, and J. Marin Effect of Salmeterol on Seasonal Changes in Airway Responsiveness and Exhaled Nitric Oxide in Pollen-Sensitive Asthmatic Subjects* Chest, September 1, 2002; 122(3): 798 - 805. [Abstract] [Full Text] [PDF]

				D. Giannini, A. Di Franco, E. Bacci, F. L. Dente, M. L. Bartoli, B. Vagaggini, and P. Paggiaro Tolerance to the Protective Effect of Salmeterol on Allergen Challenge Can Be Partially Restored by the Withdrawal of Salmeterol Regular Treatment Chest, June 1, 2001; 119(6): 1671 - 1675. [Abstract] [Full Text] [PDF]

				W. J. CALHOUN, K. L. HINTON, and J. J. KRATZENBERG The Effect of Salmeterol on Markers of Airway Inflammation Following Segmental Allergen Challenge Am. J. Respir. Crit. Care Med., March 15, 2001; 163(4): 881 - 886. [Abstract] [Full Text]

				D. Giannini, A. Di Franco, E. Bacci, F. L. Dente, M. Taccola, B. Vagaggini, and P. Paggiaro The Protective Effect of Salbutamol Inhaled Using Different Devices on Methacholine Bronchoconstriction Chest, May 1, 2000; 117(5): 1319 - 1323. [Abstract] [Full Text] [PDF]

				J. A. NIGHTINGALE, D. F. ROGERS, and P. J. BARNES Differential Effect of Formoterol on Adenosine Monophosphate and Histamine Reactivity in Asthma Am. J. Respir. Crit. Care Med., June 1, 1999; 159(6): 1786 - 1790. [Abstract] [Full Text]

				D. Taylor, M. Jensen, S. Aikman, J. Harris, P. Barnes, and B. O'Connor Comparison of salmeterol and albuterol-induced bronchoprotection against adenosine monophosphate and histamine in mild asthma Am. J. Respir. Crit. Care Med., December 1, 1997; 156(6): 1731 - 1737. [Abstract] [Full Text]