Rosiglitazone elicits in vitro relaxation in airways and precision cut lung slices from a mouse model of chronic allergic airways disease

Chantal Donovan, Simon R Bailey, Jenny Tran, Gertruud Haitsma, Zaridatul Aini Ibrahim, Simon R Foster, Mimi L K Tang, Simon G Royce, Jane E Bourke

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14 Citations (Scopus)

Abstract

Rosiglitazone (RGZ), a Peroxisome Proliferator Activated Receptor gamma (PPARgamma) ligand, is a novel dilator of small airways in mouse precision cut lung slices (PCLS). In this study, relaxation to RGZ and beta-adrenoceptor agonists were compared in trachea from naive mice and guinea pigs, and trachea and PCLS from a mouse model of chronic allergic airways disease (AAD). Airways were pre-contracted with methacholine before addition of PPARgamma ligands (RGZ, ciglitazone (CGZ) or 15-deoxy-PGJ2) or beta-adrenoceptor agonists (isoprenaline, salbutamol). Effects of T0070907 and GW9662 (PPARgamma antagonists) or epithelial removal on relaxation were assessed. Changes in force of trachea and lumen area in PCLS were measured using preparations from saline-challenged mice and mice sensitised (days 0, 14) and challenged with ovalbumin (3 times/week, 6 weeks). RGZ and CGZ elicited complete relaxation with greater efficacy than beta-adrenoceptor agonists in mouse airways but not guinea pig trachea, while 15-deoxy-PGJ2 did not mediate bronchodilation. Relaxation to RGZ was not prevented by T0070907 or GW9662, or by epithelial removal. RGZ-induced relaxation was preserved in trachea and increased in PCLS after ovalbumin-challenge. Although RGZ was less potent than beta-adrenoceptor agonists, its effects were additive with SALB and ISO, and only RGZ maintained potency and full efficacy in maximally contracted airways or after allergen challenge. Acute PPARgamma-independent, epithelial-independent airway relaxation to RGZ is resistant to functional antagonism and maintained in both trachea and PCLS from a model of chronic AAD. These novel efficacious actions of RGZ support its therapeutic potential in asthma when responsiveness to beta-adrenoceptor agonists is limited.
Original languageEnglish
Pages (from-to)1219 - 1228
Number of pages10
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume309
Issue number10
DOIs
Publication statusPublished - 2015

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