Furosemide-Induced Bronchodilation in the Rat Bronchus: Evidence of a Role for Prostaglandins
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© Springer-Verlag New York Inc. 1997
Furosemide-Induced Bronchodilation in the Rat Bronchus: Evidence of a Role for Prostaglandins J. J. Almirall, C. S. Dolman, and D. H. Eidelman Meakins-Christie Laboratories, Montreal Chest Research Institute, Royal Victoria and Montreal General Hospitals, McGill University, Montreal, Quebec Canada H2X 2P2
Abstract. Pretreatment with inhaled fuorsemide has been shown to protect against bronchoconstrictive stimuli that indirectly activate airway smooth muscle. However, it is controversial as to whether furosemide acts directly on airway smooth muscle. To investigate this we studied the effect of furosemide on both methacholine (MCh)- and serotonin (5-HT)-induced bronchoconstriction in explanted rat airways. Lungs from 21 Sprague-Dawley rats (269 ± 15 g) were excised, inflated with agarose solution at 37°C (1% w/v, 48 ml/kg), embedded in 4% agarose, and refrigerated to gel the agarose. Lung slices (0.5–1.0 mm thick) were cultured overnight at 37°C. Explants were placed on a dissecting video microscope, and airway area was measured with an image analysis system. MCh or 5-HT was administered directly to explanted airways (final concentrations 3.8 × 10−6 M and 3.8 × 10−5 M, respectively). Five min later furosemide (3.7 × 10−5 M or 3.7 × 10−4 M) was added and airway area monitored 5, 10, 15, 30, and 60 min later. Results were expressed as a percentage of the maximal response. Significant bronchodilation was seen after 30 min in airways preconstricted with MCh and after 15 min in those preconstricted with 5-HT following 3.7 × 10−4 M furosemide (p < 0.05). 3.7 × 10−5 M furosemide caused bronchodilation only at 60 min in airways constricted with 5-HT. The effect was blocked by a 30-min incubation of explants with 10−6 M indomethacin. The furosemide-induced bronchodilation effect was not observed in airways strongly constricted with 3.8 × 10−5 M MCh. These findings indicate that in the rat at least, furosemide induces a weak bronchodilator effect present only at high doses, which seems to be dependent on the production of prostaglandins. This effect may be relevant to the observed therapeutic action of furosemide in asthmatics. Key words: Furosemide—Methacholine—Serotonin—Indomethacin—Rat airways
Offprint requests to: Dr. D. H. Eidelman, Meakins-Christie Laboratories, McGill University, 3626 St. Urbain St., Montreal, Quebec Canada H2X 2P2.
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Introduction Furosemide is a loop diuretic that has been shown to protect against bronchoconstrictive stimuli that indirectly activate airway smooth muscle. For example, furosemide has been shown to modulate airway responses to ultrasonically nebulized water [12, 19], exercise [2], hypertonic solutions [11, 20], cold air [7], and to inhaled allergens [1]. The exact mechanism of this protective effect is unknown and potentially multifactorial, involving actions on neural traffic, ionic transport, production of prostaglandins, or through a vasodilator effect [10]. On the other hand, it is controversial as to whether furosemid
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