Oral administration of sodium butyrate attenuates inflammation and mucosal lesion in experimental acute ulcerative colitis
Autor: | Talita Mayra Resende Ferreira, Ana Maria Caetano Faria, Ana Cristina Gomes-Santos, Érica Leandro Marciano Vieira, Nathalia Ribeiro Mota Beltrao, Alda J. Leonel, Thaís F. Costa, Maria do Carmo Gouveia Peluzio, Alexandre P. Sad, Denise Carmona Cara, Jacqueline I. Alvarez-Leite |
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Rok vydání: | 2010 |
Předmět: |
Male
medicine.medical_specialty Endocrinology Diabetes and Metabolism Clinical Biochemistry Administration Oral Butyrate Biochemistry Gastroenterology chemistry.chemical_compound Mice Intestinal mucosa Oral administration Internal medicine medicine Animals Intestinal Mucosa Molecular Biology Mice Inbred BALB C Nutrition and Dietetics business.industry Sodium butyrate Eosinophil medicine.disease Ulcerative colitis Small intestine Interleukin-10 Butyrates medicine.anatomical_structure chemistry Immunology Acute Disease Colitis Ulcerative Lymph business |
Zdroj: | The Journal of nutritional biochemistry. 23(5) |
ISSN: | 1873-4847 |
Popis: | Butyrate is a four-carbon short-chain fatty acid that improves colonic trophism. Although several studies have shown the benefits of butyrate enemas in ulcerative colitis (UC), studies using the oral route are rare in the literature. In the present study, we evaluated the effect of butyrate intake in the immune response associated to UC. For that, mice were fed control or butyrate (0.5% sodium butyrate) diets for 14 days. Acute UC was induced by dextran sulphate sodium (DSS, 2.5%), replacing drinking water. The results showed that, in UC animals, oral butyrate significantly improved trophism and reduced leukocyte (eosinophil and neutrophil) infiltration in the colon mucosa and improved the inflammatory profile (activated macrophage, B and T lymphocytes) in cecal lymph nodes. In the small intestine, although mucosa histology was similar among groups, DSS treatment reduced duodenal transforming growth factor-β, increased interleukin-10 concentrations and increased memory T lymphocytes and dendritic cells in Peyer's patches. Butyrate supplementation was able to revert these alterations. When cecal butyrate concentration was analyzed in cecal content, it was still higher in the healthy animals receiving butyrate than in the UC+butyrate and control groups. In conclusion, our results show that oral administration of sodium butyrate improves mucosa lesion and attenuates the inflammatory profile of intestinal mucosa, local draining lymph nodes and Peyer's patches of DSS-induced UC. Our results also highlight the potential use of butyrate supplements as adjuvant in UC treatment. |
Databáze: | OpenAIRE |
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