Journal
STEROIDS
Volume 95, Issue -, Pages 88-95Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.steroids.2014.12.016
Keywords
Corticosteroid; Isoxazoline; Ovalbumin; Nuclear translocation; PK profile; GILZ
Ask authors/readers for more resources
A novel glucocorticoids series of (GCs), 6 alpha,9 alpha-di-Fluoro 3-substituted C-16,17-isoxazolines was designed, synthesised and their structure activity relationship was evaluated with glucocorticoid receptor (GR) binding studies together with GR nuclear translocation cell-based assays. This strategy, coupled with in silica modelling analysis, allowed for the identification of Cpd #15, an isoxazoline showing a sub-nanomolar inhibitory potency (IC50 = 0.84 nM) against TNF alpha-evoked IL-8 release in primary human airways smooth muscle cells. In Raw264.7 mouse macrophages, Cpd #15 inhibited LPS-induced NO release with a potency (IC50 = 6 nM) > 10-fold higher with respect to Dexamethasone. Upon intratracheal (it.) administration, Cpd #15, at 0.1 mu mol/kg significantly inhibited and at 1 mu mol/kg fully counteracted eosinophilic infiltration in a model of allergen-induced pulmonary inflammation in rats. Moreover, Cpd #15 proved to be suitable for pulmonary topical administration given its sustained lung retention (t(1/2) = 6.5 h) and high pulmonary levels (>100-fold higher than plasma levels) upon intratracheal administration in rats. In summary, Cpd #15 displays a pharmacokinetic and pharmacodynamic profile suitable for topical treatment of conditions associated with pulmonary inflammation such as asthma and COPD. (C) 2015 Elsevier Inc. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available