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Effect of aerosolized administration of KF19514, a phosphodiesterase 4 inhibitor, on bronchial hyperresponsiveness and airway inflammation induced by antigen inhalation in guinea‐pigs
Author(s) -
Shigeharu Myou,
Masaki Fujimura,
Kazuyoshi Kurashima,
Hideki Tachibana,
Toshiharu Hirose,
Shinji Nakao
Publication year - 2000
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1046/j.1365-2222.2000.00782.x
Subject(s) - bronchoconstriction , inhalation , methacholine , bronchoalveolar lavage , medicine , asthma , immunology , pharmacology , ovalbumin , antigen , bronchial hyperresponsiveness , airway , anesthesia , lung , respiratory disease
Background Although phosphodiesterase (PDE) 3 and 4 inhibitors have received much attention for the treatment of bronchial asthma, systemic adverse effects have also been reported. Objective The purpose of this study was to investigate the effect of inhaled olprinone, a newly developed PDE3 inhibitor, and KF19514, a PDE1 and 4 inhibitor, on antigen‐induced airway reactions in guinea‐pigs. Methods Fifteen minutes after inhalation of olprinone (0.1 or 1.0 mg/mL) and KF19514 (0.1 or 0.01 mg/mL), animals were given an antigen challenge. Bronchial hyper‐responsiveness and bronchoalveolar lavage fluid cell analysis were performed 24 h after the antigen challenge. Results Inhalation of olprinone and KF19514 caused a dose‐related inhibition of antigen‐induced bronchoconstriction. Antigen inhalation significantly increased bronchoconstrictor responses to methacholine, and airway accumulation of neutrophils and eosinophils, 24 h after the antigen challenge. These responses were dose‐dependently prevented by KF19514, but not by olprinone. Conclusion The results indicate that inhaled PDE inhibitors might be useful for treatment of bronchial asthma.