Abstract

The short chain fatty acids (SCFA) are the best nutrients for the colonocytes. Glucose is poorly used as a fuel but may be transformed into SCFA by colonic bacteria. The aim of this study was to investigate the effect of SCFA or glucose on experimental colitis. Colitis was induced in 30 Wistar rats by colonic instillation of 4% acetic acid. Five days later they were randomized to receive twice a day colonic lavage containing saline (controls, N = 10), 10% hypertonic glucose (N = 10) or SCFA (N = 10) until day 8 when they were killed. At autopsy, the colon was removed and weighed and the mucosa was evaluated macro- and microscopically and stripped out for DNA assay. Data are reported as mean +/- SD or median [range] as appropriate. All animals lost weight but there was no difference between groups. Colon weight was significantly lower in the SCFA group (3.8 +/- 0.5 g) than in the control (5.3 +/- 2.1 g) and glucose (5.2 +/- 1.3 g) groups (P<0.05). Macroscopically, the severity of inflammation was less in SCFA (grade 2 [1-5]) than in control (grade 9 [4-10]) and glucose-treated (grade 9 [2-10]) animals (P<0.01). Microscopically, ulceration of the mucosa was more severe in the glucose and control groups than in the SCFA group. The DNA content of the mucosa of SCFA-treated animals (8.2 [5.0-20.2] mg/g of tissue) was higher than in glucose-treated (5.1 [4.2-8.5] mg/g of tissue; P<0.01) and control (6.2 [4.5-8.9] mg/g of tissue; P<0.05) animals. We conclude that SCFA may enhance mucosal re-epithelialization in experimental colitis, whereas hypertonic glucose is of no benefit.

Highlights

  • The treatment of non-complicated ulcerative colitis is aimed at reducing the inflammatory reaction and healing the colonic epithelium

  • One animal from the hypertonic glucose group died on the 6th day after induction of colitis

  • The weight of the colon was significantly lower in the short chain fatty acids (SCFA) group (3.8 ± 0.5 g) than in both the control (5.3 ± 2.1 g) and glucose (5.2 ± 1.3 g) groups (P

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Summary

Introduction

The treatment of non-complicated ulcerative colitis is aimed at reducing the inflammatory reaction and healing the colonic epithelium. Corticosteroids, 5-aminosalicylic acid compounds and immunosuppressants are the drugs most frequently used [1]. In patients with ulcerative colitis, the fecal concentration of short chain fatty acids (SCFA) seems to be diminished and apparently the oxidation of these nutrients is impaired by the colonic mucosa cells [2,3]. SCFA are the best nutrients for the colonocytes and provide up to 70% of the energy supply to the mucosa [3]. Propionate and acetate, the most important SCFA, have a direct trophic action on the colonic mucosa.

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