Anti-inflammatory and anti-oxidant activities of olmesartan medoxomil ameliorate experimental colitis in rats
Autor: | Mariane G. Tadros, Amani E. Khalifa, Marwa M. Nagib, Moushira I. ELSayed |
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Rok vydání: | 2013 |
Předmět: |
Male
medicine.medical_specialty Angiotensin receptor Anti-Inflammatory Agents Administration Oral Tetrazoles Pharmacology Toxicology Inflammatory bowel disease Antioxidants Proinflammatory cytokine Sulfasalazine Internal medicine medicine Animals Rats Wistar Colitis Olmesartan Medoxomil Dose-Response Relationship Drug Chemistry Dextran Sulfate Imidazoles medicine.disease Angiotensin II Ulcerative colitis Rats Disease Models Animal Endocrinology Colitis Ulcerative Olmesartan medicine.drug |
Zdroj: | Toxicology and Applied Pharmacology. 271:106-113 |
ISSN: | 0041-008X |
DOI: | 10.1016/j.taap.2013.04.026 |
Popis: | Ulcerative colitis (UC) is a chronic inflammatory bowel disease (IBD) driven through altered immune responses with production of proinflammatory cytokines. Many therapies are used, but side effects and loss of response limit long-term effectiveness. New therapeutic strategies are thus needed for patients who don't respond to current treatments. Recently, there is suggested involvement of the proinflammatory hormone angiotensin II in inflammatory bowel disease. The aim of this study was to investigate the possible role of olmesartan medoxomil (OLM-M), an angiotensin II receptor blocker in ameliorating ulcerative colitis. Colitis was induced in male Wistar rats by administration of 5% dextran sodium sulphate (DSS) in drinking water for 5days. OLM-M (1, 3 and 10mg/kg) was administered orally during 21days prior to the induction of colitis, and for 5days after. Sulfasalazine (500mg/kg) was used as reference drug. All animals were tested for changes in colon length, disease activity index (DAI) and microscopic damage. Colon tissue concentration/activity of tumor necrosis alpha (TNF-α), myeloperoxidase (MPO), prostaglandin E2 (PGE2), reduced glutathione (GSH) and malondialdehyde (MDA) were assessed. Results showed that the OLM-M dose-dependently ameliorated the colonic histopathological and biochemical injuries, an effect that is comparable or even better than that of the standard sulfasalazine. These results suggest that olmesartan medoxomil may be effective in the treatment of UC through its anti-inflammatory and antioxidant effects. |
Databáze: | OpenAIRE |
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