Inflammatory bowel disease (IBD) is a chronic intestinal
inflammation that is highly prevalent worldwide.
Interleukin (IL)-10 can effectively inhibit negative cascades such as the production of inflammatory mediators (
inducible nitric oxide synthase [iNOS],
cyclooxygenase-2), accumulation of inflammatory infiltrates (macrophages, eosinophils, neutrophils), toxicity (lower T cell subsets), and secretion of pro-inflammatory
cytokines (IL-1β, TNF-α) in tissues such as the spleen, mesenteric lymph nodes (MLN), Peyer's patch (PP), and colon. In this study, we investigated whether
chlorogenic acid (CHA) can regulate
inflammation in
IL-10 knockout (KO) mice used as an IBD animal model. CHA significantly increased the ratio of CD4+/CD8+, T cell subsets in PP, and MLN of
IL-10 KO mice. In addition, CHA also morphologically attenuated colon
inflammation in
IL-10 KO mice. We demonstrated that CHA significantly reduced the expression levels of iNOS, IL-1β, TNF-α, which were highly expressed in
IL-10 KO mice. Therefore, CHA may provide beneficial effects for improving IBD by decreasing
inflammations.