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      Chrysin, a natural flavone, improves murine inflammatory bowel diseases.

      Biochemical and Biophysical Research Communications
      Animals, Colon, drug effects, metabolism, pathology, Dextran Sulfate, toxicity, Disease Models, Animal, Flavonoids, therapeutic use, I-kappa B Proteins, Inflammation Mediators, Inflammatory Bowel Diseases, chemically induced, drug therapy, Intestinal Mucosa, Mice, Mice, Inbred BALB C, Protein Transport, Weight Loss

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          Abstract

          Chrysin (5,7-dihydroxyflavone) is a natural flavone commonly found in many plants. It has previously been shown to be an anti-tumor agent. In this study, we investigated whether chrysin could alleviate the symptoms of dextran sodium sulfate (DSS)-induced colitis in mice and whether chrysin has an inhibitory effect on nuclear factor (NF)-kappaB activation in vitro. A significant blunting of weight loss and clinical signs was observed in DSS-exposed, chrysin-treated mice when compared to vehicle-treated mice. This was associated with a remarkable amelioration of the disruption of the colonic architecture, a significant reduction in colonic myeloperoxidase (MPO) activity, and a decrease in the production of inflammatory mediators such as nitric oxide (NO), prostaglandin (PG) E(2), and pro-inflammatory cytokines. In addition, chrysin inhibited tumor necrosis factor (TNF)-alpha-induced activation of NF-kappaB in IEC-6 cells. These findings suggest that chrysin exerts potentially clinically useful anti-inflammatory effects mediated through the suppression of NF-kappaB activation.

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