Abstract

Dietary fiber, with intake of soluble fibers in particular, has been reported to lower the risk for developing inflammatory bowel diseases (IBD). This is at least partly attributable to the fermentation of dietary fiber by the colonic microbiota to produce short chain fatty acids. Pectin, a widely consumed soluble fiber, is known to exert a protective effect in murine models of IBD, but the underlying mechanism remains elusive. Apart from having a prebiotic effect, it has been suggested that pectin direct influences host cells by modulating the inflammatory response in a manner dependent on its neutral sugar side chains. Here we examined the effect of the side chain content of pectin on the pathogenesis of experimental colitis in mice. Male C57BL/6 mice were fed a pectin-free diet, or a diet supplemented with characteristically high (5% orange pectin) or low (5% citrus pectin) side chain content for 10–14 days, and then administered 2,4,6-trinitrobenzene sulfonic acid or dextran sulfate sodium to induce colitis. We found that the clinical symptoms and tissue damage in the colon were ameliorated in mice that were pre-fed with orange pectin, but not in those pre-fed with citrus pectin. Although the population of CD4+Foxp+ regulatory T cells and CD4+RORγt+ inflammatory T cells in the colon were comparable between citrus and orange pectin-fed mice, colonic interleukin (IL)-1β and IL-6 levels in orange pectin-fed mice were significantly decreased. The fecal concentration of propionic acid in orange pectin-fed mice was slightly but significantly higher than that in control and citrus pectin-fed mice but the cecal concentration of propionic acid after the induction of TNBS colitis was comparable between orange and citrus pectin-fed mice. Furthermore, the protective effect of orange pectin against colitis was observed even in mice treated with antibiotics. IL-6 production from RAW264.7 cells stimulated with the toll-like receptor agonist Pam3CSK4 or lipopolysaccharide was suppressed by pre-treatment with orange pectin in vitro. Taken together, these results suggest that the side chains of pectin not only augment prebiotic effects but also directly regulate IL-6 production from intestinal host cells in a microbiota-independent fashion to attenuate colitis.

Highlights

  • Inflammatory bowel diseases (IBD) consisting mainly of ulcerative colitis and Crohn’s disease are idiopathic inflammatory disorders of the gastrointestinal tract

  • It has been previously reported that orange pectin contains 1.9 times more arabinose and 2.5 times more galactose compared with citrus pectin; the side chain lengths, average molecular weight, and degree of methyl esterification (DM) are comparable between the two [28]

  • Control mice that were fed a pectinfree diet lost more than 10% body weight and decreased their food intake by approximately 3 g on day 2 following trinitrobenzoic sulfonic acid (TNBS) challenge (Figures 1B,C)

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Summary

Introduction

Inflammatory bowel diseases (IBD) consisting mainly of ulcerative colitis and Crohn’s disease are idiopathic inflammatory disorders of the gastrointestinal tract. A high-fiber diet including soluble fibers in particular has been reported to protect against the development of IBD [7, 8], and a prospective cohort study has suggested that high, longterm intake of dietary fiber lowers the risk of Crohn’s disease by 40% [9]. This protective effect against IBD is thought to be at least partly attributable to the fermentation of dietary fiber by the colonic microbiota, which produce short chain fatty acids (SCFAs) including acetic acid, propionic acid, and butyric acid. The microbiota-independent pathway by which pectin exerts its anti-inflammatory effect is poorly understood

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