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Citation
Tags
HERO ID
7699840
Reference Type
Journal Article
Title
The intestinal anti-inflammatory effect of dersalazine sodium is related to a down-regulation in IL-17 production in experimental models of rodent colitis
Author(s)
Camuesco, D; Rodríguez-Cabezas, ME; Garrido-Mesa, N; Cueto-Sola, M; Bailón, E; Comalada, M; Arribas, B; Merlos, M; Balsa, D; Zarzuelo, A; Janer, G; Xaus, J; Román, J; Gálvez, J
Year
2012
Is Peer Reviewed?
Yes
Journal
British Journal of Pharmacology
ISSN:
0007-1188
EISSN:
1476-5381
Publisher
WILEY-BLACKWELL
Location
MALDEN
Volume
165
Issue
3
Page Numbers
729-740
Language
English
PMID
21790535
DOI
10.1111/j.1476-5381.2011.01598.x
Web of Science Id
WOS:000298953100016
Abstract
BACKGROUND AND PURPOSE:
Dersalazine sodium (DS) is a new chemical entity formed by combining, through an azo bond, a potent platelet activating factor (PAF) antagonist (UR-12715) with 5-aminosalicylic acid (5-ASA). DS has been demonstrated to have anti-inflammatory effects on trinitrobenzene sulphonic acid (TNBS)-induced colitis in rats and recently in UC patients in phase II PoC. There is Increasing evidence that Th17 cells have an important role in the pathogenesis of inflammatory bowel disease (IBD). The aim of this study was to further characterize the anti-inflammatory effects of DS.
EXPERIMENTAL APPROACH:
Effect of DS (10 or 30 mg·kg(-1) b.i.d.) on TNBS-induced colitis in rats was studied after 2 and 7 days with special focus on inflammatory mediators. Additionally, its anti-inflammatory properties were analysed in two different models of dextran sodium sulphate (DSS)-induced colitis, BALB/c and C57BL/6 mice, the latter being dependent on IL-17.
KEY RESULTS:
DS, when administered for 7 days, showed intestinal anti-inflammatory effects in TNBS-induced colitis; these effects were observed both macroscopically and through the profile of inflammatory mediators (TNF, IL-1β, IL-6 and IL-17). Although the 2 day treatment with DS did not induce intestinal anti-inflammatory effects, it was sufficient to reduce the enhanced IL-17 expression. DS showed beneficial effects on DSS-induced colitis in C57BL/6 mice and reduced colonic pro-inflammatory cytokines IL-1β, IL-6 and IL-17. In contrast, it did not exert intestinal anti-inflammatory effects on DSS-induced colitis in BALB/c mice.
CONCLUSIONS AND IMPLICATIONS:
DS exerts intestinal anti-inflammatory activity in different rodent models of colitis through down-regulation of IL-17 expression.
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