Literature DB >> 7831623

Effect of acetazolamide and amiloride against sodium metabisulphite-induced bronchoconstriction in mild asthma.

B J O'Connor1, C T Yeo, Y M Chen-Worsdell, P J Barnes, K F Chung.   

Abstract

BACKGROUND: Inhaled frusemide but not bumetanide, another loop diuretic, reduces bronchial responsiveness to sodium metabisulphite (MBS). To investigate whether the effect of frusemide could be mediated through mechanisms other than Na+/K+/Cl- cotransporter inhibition, the effects of amiloride--an inhibitor of sodium channels in the airway epithelium--and of acetazolamide--a specific inhibitor of carbonic anhydrase--against MBS challenge were studied.
METHODS: In two separate randomised double blind placebo controlled studies, 10 subjects with mild asthma attended on four separate occasions to inhale 7.5 mg amiloride or matched placebo, and 500 mg acetazolamide or placebo, immediately before MBS challenge. The concentration of MBS required to cause a 20% fall in baseline FEV1 (PC20) was measured.
RESULTS: Amiloride and acetazolamide had no effect on baseline FEV1. Amiloride had no effect against MBS challenge, but acetazolamide increased -log PC20 from a mean (SE) of 0.75 (0.09) to 0.98 (0.06) representing a 0.77 (0.24) doubling dose increase.
CONCLUSIONS: These results suggest that carbonic anhydrase activity in the airways, but not sodium flux, modulates bronchial responsiveness to MBS challenge. The action of frusemide is not likely to involve inhibition of carbonic anhydrase activity.

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Year:  1994        PMID: 7831623      PMCID: PMC475268          DOI: 10.1136/thx.49.11.1096

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  16 in total

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5.  Immunocytochemical localization of carbonic anhydrase in myelinated fibers in peripheral nerves of rat and mouse.

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9.  Furosemide acutely decreases airways resistance in chronic bronchopulmonary dysplasia.

Authors:  L C Kao; D Warburton; C W Sargent; A C Platzker; T G Keens
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Authors:  K F Chung; G Dent; P J Barnes
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