| Literature DB >> 27771081 |
Daline Fernandes de Souza Araújo1, Gerlane Coelho Bernardo Guerra2, Raimundo Fernandes de Araújo Júnior3, Aurigena Antunes de Araújo4, Paloma Oliveira Antonino de Assis5, Ariosvaldo Nunes de Medeiros6, Yasmim Regis Formiga de Sousa1, Maria Manuela Estevez Pintado7, Julio Gálvez8, Rita de Cássia Ramos do Egypto Queiroga5.
Abstract
Complementary or alternative medicine is of great interest for the treatment of inflammatory bowel disease, with the aim of ameliorating the side effects of the drugs commonly used or improving their efficacy. In this study, we evaluated the ability of goat whey to prevent intestinal inflammation in the experimental model of acetic acid-induced rats and compared it to sulfasalazine. Pretreatment with goat whey (1, 2, and 4g/kg) and sulfasalazine (250mg/kg) on colitic rats improved colonic inflammatory markers, including myeloperoxidase activity, leukotriene B4 levels, as well as the production of proinflammatory cytokines IL-1β and tumor necrosis factor-α. Furthermore, the administration of goat whey significantly reduced the colonic oxidative stress by reducing malondialdehyde levels and increased total glutathione content, a potent antioxidant peptide. The histological evaluation of the colonic specimens from colitic rats confirmed these beneficial effects, as goat whey preserved the colonic tissue, especially in those rats treated with the highest dose of goat whey or with sulfasalazine. The immunohistochemistry analysis of the colonic tissue evaluation also revealed a reduction in the expression of cyclooxygenase-2, inducible nitric oxide synthase, and matrix metalloproteinase-9, together with an increased expression of suppressor of cytokine signaling-1. These results suggest that goat whey exerted a preventive effect against the intestinal damage induced by acetic acid, showing a similar efficacy to that shown by sulfasalazine, therefore making it a potential treatment for human inflammatory bowel disease.Entities:
Keywords: cytokines; goat whey; immunohistochemical; intestinal inflammation; oxidative stress
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Year: 2016 PMID: 27771081 DOI: 10.3168/jds.2016-10930
Source DB: PubMed Journal: J Dairy Sci ISSN: 0022-0302 Impact factor: 4.034