Open AccessEffects of inhaled furosemide on platelet‐activating factor challenge in mild asthma
Author(s) -
Echazarreta A.l,
Gómez F.p,
Ribas J,
Achaval M,
Barberà J.a,
Roca J,
Chung K.f,
RodriguezRoisin R
Publication year - 1999
Publication title -
european respiratory journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.021
H-Index - 241
eISSN - 1399-3003
pISSN - 0903-1936
DOI - 10.1034/j.1399-3003.1999.14c22.x
Subject(s) - platelet activating factor , asthma , furosemide , medicine , leukotriene , bronchoconstriction , respiratory system , proinflammatory cytokine , placebo , inhalation , anesthesia , platelet , platelet activation , leukotriene b4 , mediator , leukotriene d4 , pharmacology , immunology , inflammation , pathology , alternative medicine
Furosemide (Fur) may have an anti‐inflammatory effect on airways in patients with asthma although its intrinsic mechanism remains elusive. Platelet‐activating factor (PAF) is a potent proinflammatory mediator that induces systemic and respiratory effects in normal control subjects and asthmatics. The aim of this study was to assess whether pretreatment with nebulized Fur (40 mg) was able to modulate PAF‐induced systemic and respiratory effects in asthma. Eleven patients were studied (mean± sem 22±0.8 yrs) with mild asthma (forced expiratory volume in one second, 95±4%) in a randomized, double‐blind, placebo‐controlled, cross‐over fashion, one week apart. PAF challenge (18 µg) was carried out 15 min after administration of Fur or placebo. Peripheral blood neutrophils, respiratory system resistance, and arterial blood gases were measured at baseline, and 5, 15 and 45 min after PAF; urinary cysteinyl leukotriene E 4 (uLTE 4 ) was also measured, at baseline and 120 min after PAF challenge. Although Fur did not alter PAF‐induced systemic and respiratory effects, it did partially inhibit (63%; p<0.04) the increments of uLTE 4 levels shown after PAF inhalation. It is concluded that furosemide is not effective in protecting against platelet‐activating factor challenge in patients with asthma despite its potential inhibition of leukotriene synthesis. These findings reinforce the view that the pulmonary effects of platelet‐activating factor are mediated through different pathways. Eur Respir J 1999; 14: 616–621.