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Mediators Inflamm ; 2014: 393217, 2014.
Article in English | MEDLINE | ID: mdl-24891765

ABSTRACT

BACKGROUND: Aeromonas hydrophila is an opportunistic bacterial pathogen that is associated with a number of human diseases. Hesperidin (HES) has been reported to exert antioxidant and anti-inflammatory activities. OBJECTIVES: The aim of this study was to investigate the potential effect of HES treatment on inflammatory response induced by A. hydrophila infection in murine. METHODS: A. hydrophila-infected mice were treated with HES at 250 mg/kg b.wt./week for 4 consecutive weeks. Phagocytosis, reactive oxygen species production, CD4(+)/CD8(+) T cell ratio, and CD14 expression on intestinal infiltrating monocytes were evaluated. The expression of E-selectin and intercellular adhesion molecule 1 on stimulated HUVECs and RAW macrophage was evaluated. RESULTS: Percentage of CD4(+) T cells in the intestinal tissues of infected treated mice was highly significantly increased; however, phagocytic index, ROS production, CD8(+) T cells percentage, and CD14 expression on monocytes were significantly reduced. On the other hand, HES significantly inhibited A-LPS- and A-ECP-induced E-selectin and ICAM-1 expression on HUVECs and ICAM-1 expression on RAW macrophage. CONCLUSION: Present data indicated that HES has a potential role in the suppression of inflammatory response induced by A. hydrophila toxins through downmodulation of ROS production and CD14 and adhesion molecules expression, as well as increase of CD4(+)/CD8(+) cell ratio.


Subject(s)
Aeromonas hydrophila , CD4-CD8 Ratio , Gram-Negative Bacterial Infections/blood , Gram-Negative Bacterial Infections/immunology , Hesperidin/pharmacology , Inflammation/immunology , Animals , Body Weight , CD4-Positive T-Lymphocytes/cytology , CD8-Positive T-Lymphocytes/cytology , Cell Separation , Flow Cytometry , Human Umbilical Vein Endothelial Cells , Humans , Lipopolysaccharide Receptors/metabolism , Lipopolysaccharides/chemistry , Macrophages/metabolism , Male , Mice , Organ Size , Phagocytosis , Reactive Oxygen Species/metabolism
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