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Gelatin tannate reduces the proinflammatory effects of lipopolysaccharide in human intestinal epithelial cells.
- Source :
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Clinical and experimental gastroenterology [Clin Exp Gastroenterol] 2012; Vol. 5, pp. 61-7. Date of Electronic Publication: 2012 May 08. - Publication Year :
- 2012
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Abstract
- Background: Gelatin tannate is a mixture of tannic acid and gelatin. Tannic acid has astringent properties, due to its capacity to form protein-macromolecular complexes, as well as antibacterial and antioxidant properties. However, little is known about its anti-inflammatory properties.<br />Purpose: To evaluate the anti-inflammatory activity of gelatin tannate by quantifying the suppression of key molecules produced during inflammatory events in lipopolysaccharide (LPS)-stimulated human intestinal cells.<br />Methods: Intercellular adhesion molecule-1 (ICAM-1) expression was determined by Western blot analysis; interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α) concentrations were measured by enzyme-linked immunosorbent assays in Caco-2 cells 24 hours after treatment with LPS (1 μg/mL) in presence of different concentrations of gelatin tannate.<br />Results: ICAM-1 is induced on a wide variety of cells by inflammatory stimuli such as LPS. Our results have shown gelatin tannate as a potent inhibitor of ICAM-1 expression in LPS-stimulated Caco-2 cells. IL-8 and TNF-α are important inflammatory mediators, recruiting neutrophils and T-lymphocytes. Together with LPS, adding gelatin tannate at different concentrations induced a dose-dependent inhibition of IL-8 and TNF-α released by Caco-2 cells.<br />Conclusion: These results suggest that gelatin tannate exerts anti-inflammatory effects by inhibiting the specific cytokines and adhesion molecules involved in several inflammatory disorders.
Details
- Language :
- English
- ISSN :
- 1178-7023
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Clinical and experimental gastroenterology
- Publication Type :
- Academic Journal
- Accession number :
- 22629114
- Full Text :
- https://doi.org/10.2147/CEG.S28792