H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats

Hydrogen sulfide (H 2 S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful...

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Veröffentlicht in:Inflammopharmacology 2018-04, Vol.26 (2), p.479-489
Hauptverfasser: Kupai, Krisztina, Almási, Nikoletta, Kósa, Magdolna, Nemcsók, János, Murlasits, Zsolt, Török, Szilvia, Al-awar, Amin, Baráth, Zoltán, Pósa, Anikó, Varga, Csaba
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Sprache:eng
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Zusammenfassung:Hydrogen sulfide (H 2 S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful stimuli, were found to regulate intestinal inflammation in experimental animal models of colitis. We aimed to investigate the protective effects of H 2 S against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats, and whether HO enzyme system is involved in the H 2 S-induced colonic cytoprotection. Male Wistar rats were treated with TNBS to induce colitis, and H 2 S donor (Lawesson’s reagent) was prepared two times/day at different concentrations, and delivered per os (from day 1 to day 3). Our results suggest that daily treatment (2 times/day) with H 2 S donor, could significantly decrease the extent of colonic inflammation compared to vehicle treatment, and the most effective daily dose of H 2 S donor against inflammation was 18.75 µM/kg/day. Per os administration of H 2 S donor increased the colonic HO enzyme activity; on the contrary, the protective effect of H 2 S was abolished by the co-treatment with HO inhibitor. Our findings suggest that H 2 S confers colonoprotection, probably by modulation of anti-inflammatory parameters and HO enzyme activity.
ISSN:0925-4692
1568-5608
DOI:10.1007/s10787-017-0382-8