Literature DB >> 15575933

Differential effects of fluticasone and montelukast on allergen-induced asthma.

M Palmqvist1, C Bruce, M Sjöstrand, P Arvidsson, J Lötvall.   

Abstract

Early asthmatic responses (EAR) and late asthmatic responses (LAR) to allergen are induced by the local release of a series of bronchoconstrictor mediators, including leukotrienes and histamine. Both anti-leukotrienes and other anti-asthma drugs, such as inhaled glucocorticoids, have been shown to reduce both EAR and LAR. The aim of the present study was to directly compare the effects of regular treatment with an oral anti-leukotriene, montelukast (Mont; 10 mg once daily, for 8 days), and an inhaled glucocorticoid [fluticasone propionate (FP) 250 microg twice daily for 8 days] on the EAR and LAR to an inhaled allergen challenge. Patients with a documented EAR and LAR at a screening visit were randomized to these treatments, or placebo, in a double-blind, double-dummy, crossover fashion. Allergen challenge at a dose causing both an EAR and LAR was given on the eighth day of treatment. The maximum fall in FEV1 during the EAR was 17.8% during placebo treatment, 8.3% during Mont and 16.3% during FP (P <0.05 for Mont vs placebo). The maximum fall during the EAR was 13.8% during placebo treatment, 11.8% during Mont and 2% during FP treatment (P <0.05 for FP vs placebo and FP vs Mont). PC20 methacholine was significantly higher 24 h after allergen challenge during FP-treatment compared with Mont (P <0.05). Both montelukast and fluticasone reduced the relative amount of sputum eosinophils after allergen compared with placebo treatment. This study shows that anti-leukotrienes are effective to attenuate the EAR, whereas inhaled glucocorticoids are more effective than anti-leukotrienes in attenuating the EARs and improves bronchial hyperresponsiveness to a greater extent. In conclusion, inhaled glucocorticoids have overall greater efficacy than oral anti-leukotrienes to attenuate allergen-induced airway responses in mild asthmatic patients.

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Year:  2005        PMID: 15575933     DOI: 10.1111/j.1398-9995.2005.00633.x

Source DB:  PubMed          Journal:  Allergy        ISSN: 0105-4538            Impact factor:   13.146


  8 in total

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2.  Cysteinyl leukotriene antagonism inhibits bronchoconstriction in response to hypertonic saline inhalation in asthma.

Authors:  Shamsah Kazani; Jonathan Sadeh; Sreedhar Bunga; Michael E Wechsler; Elliot Israel
Journal:  Respir Med       Date:  2010-12-18       Impact factor: 3.415

3.  The inhaled phosphodiesterase 4 inhibitor GSK256066 reduces allergen challenge responses in asthma.

Authors:  Dave Singh; Frank Petavy; Alex J Macdonald; Aili L Lazaar; Brian J O'Connor
Journal:  Respir Res       Date:  2010-03-01

4.  Allergen-induced airway inflammation and its therapeutic intervention.

Authors:  Paul M O'Byrne
Journal:  Allergy Asthma Immunol Res       Date:  2009-09-25       Impact factor: 5.764

5.  Comparing the effects of two inhaled glucocorticoids on allergen-induced bronchoconstriction and markers of systemic effects, a randomised cross-over double-blind study.

Authors:  Jan Lötvall; Mona Palmqvist; Peter Arvidsson
Journal:  Clin Transl Allergy       Date:  2011-10-31       Impact factor: 5.871

6.  LPS exacerbates functional and inflammatory responses to ovalbumin and decreases sensitivity to inhaled fluticasone propionate in a guinea pig model of asthma.

Authors:  A P P Lowe; R S Thomas; A T Nials; E J Kidd; K J Broadley; W R Ford
Journal:  Br J Pharmacol       Date:  2015-03-24       Impact factor: 8.739

7.  The effect of the novel phosphodiesterase-4 inhibitor MEM 1414 on the allergen induced responses in mild asthma.

Authors:  Brian R Leaker; Dave Singh; Ferhana Y Ali; Peter J Barnes; Brian O'Connor
Journal:  BMC Pulm Med       Date:  2014-10-28       Impact factor: 3.317

8.  Route of Administration Affects Corticosteroid Sensitivity of a Combined Ovalbumin and Lipopolysaccharide Model of Asthma Exacerbation in Guinea Pigs.

Authors:  Alexander P P Lowe; Rhian S Thomas; Anthony T Nials; Emma J Kidd; Kenneth J Broadley; William R Ford
Journal:  J Pharmacol Exp Ther       Date:  2017-06-02       Impact factor: 4.030

  8 in total

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