Participation of the intestinal microbiota in the mechanism of beneficial effect of treatment with synbiotic Syngut on experimental colitis under stress conditions

摘要

gut-brain axis plays a central role in the regulation of stress related diseases such as irritable bowel syndrome (iBs) or inflammatory bowel disease (iBD). it is increasingly recognized that stress modulates gut microbiota community structure and activity and represents an important causal factor in dysbiosis. this study was designed to determine the effect of daily treatment with synbiotic (syngut) containing inulin, Lactobacillus acidophilus, Bifidobacterium lactis w51, Lactobacillus plantarum w21 and Lactococcus lactis applied i.g. at a dose of 50 mg/kg i.g. on the colonic damage and colonic mucosal blood flow in rats with experimentally induced tnBs-colitis that were additionally exposed or not to acute stress (episodes of cold restraint stress every other day before colitis induction). Control rats received daily treatment with vehicle (saline, i.g.) or mesalazine (50 mg/kg-d i.g.), the standard drug recommended in therapy of iBD. at the termination of tnBs colitis, the histologic evaluation of colonic mucosa, mucosal malonyldialdehyde (MDa) level and plasma concentrations of proinflammatory cytokines (tnf-α, iL-1β) and adipokine adiponectin were assessed. the samples of colonic mucosa not involving colonic lesions and surrounding the flared mucosa were excised for the determination of mrna expression for proinflammatory biomarkers tnf-α, iL-1β, iL-10 and Cox-2 as well as antioxidazing factors soD-1 and soD-2. finally, the gut microbial profiles were analyzed by 16s rrna sequencing at phylum, family and genus level. episodes of cold stress significantly aggravated the course of tnBs colitis, and significantly increased the release of proinflammatory cytokines as well as the significant increase in the MDa concentration has been observed as compared with non-stressed tnBs rats. these changes were followed by the significant fall in the CBf and plasma adiponectin levels and by the overexpression of mrna of proinflammatory biomarkers. synbiotic treatment with syngut significantly reduced the area of colonic lesions observed macroscopically and microscopically in rats with tnBs colitis with or without exposure to cold stress, significantly increased the CBf, normalized plasma adiponectin levels and significantly attenuated the release and colonic expression of proinflammatory cytokines and biomarkers. the analysis of the gut microbiota showed a significant reduction of microbial diversity (shannon index) in rats with tnBs colitis with or without exposure to stress. the therapy with syngut failed to significantly affect the alpha diversity. at the phylum level, the significant rise in Proteobacteria has been observed in stressed rats with tnBs colitis and this effects was attenuated by treatment with syngut. at family level, tnBs colitis alone or in combination with stress led to a significant decrease of sCfa producing bacterial taxa such as Ruminococaceae and Lachnospiraceae and syngut counteracted this effect. we conclude that: 1) cold stress exacerbates the gastrointestinal inflammation in experimental colitis; 2) the synbiotic therapy with syngut ameliorates the gut inflammation in rats with tnBs colitis combined with cold stress; 3) the beneficial effect of syngut is accompanied by increase of anti-inflammatory taxa such as Ruminococaceae and Lachnospiraceae, and 4) the modulation of gut microbiota with syngut alleviates stress- related intestinal inflammation suggesting a potential usefulness of synbiotic therapy in intestinal disorders accompanied by stress in patients with iBD.