Insulin alleviates murine colitis through microbiome alterations and bile acid metabolism

• Published in: Journal of translational medicine 2023-07, Vol.21 (1), p.498-498, Article 498
• Main Authors: He, Shuying, Li, Jiating, Yao, Zirong, Gao, Zixian, Jiang, Yonghong, Chen, Xueqing, Peng, Liang
• Format: Article
• Language: English
• Subjects: Acids; Animal models; Antibodies; Bile acid metabolism; Colitis; Colon; Complications and side effects; Diagnosis; Digestive system; Drinking water; Ethanol; Fecal microflora; Feces; Gastrointestinal tract; Genes; Glucose; Gut microbiota; Health aspects; Inflammation; Inflammatory bowel disease; Inflammatory bowel diseases; Insulin; Intestinal microflora; Intestine; Laboratory animals; Lithocholic acid; Macrophage; Macrophages; Metabolomics; Microbiomes; Microbiota; rRNA 16S; Transplantation; Transplants & implants
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-023-04214-3

Insulin has been reported to exhibit anti-inflammatory activities in the context of bowel inflammation. However, the role of the interaction between insulin and the microbiota in gut health is unclear. Our goal was to investigate the mechanism of action of insulin in bowel inflammation and the relationship between insulin and the gut microbiota. We used acute and chronic murine models of inflammatory bowel disease (IBD) to evaluate whether insulin influences the progression of colitis. Colonic tissues, the host metabolome and the gut microbiome were analyzed to investigate the relationship among insulin treatment, the microbiome, and disease. Experiments involving antibiotic (Abx) treatment and fecal microbiota transplantation (FMT) confirmed the association among the gut microbiota, insulin and IBD. In a series of experiments, we further defined the mechanisms underlying the anti-inflammatory effects of insulin. We found that low-dose insulin treatment alleviated intestinal inflammation but did not cause death. These effects were dependent on the gut microbiota, as confirmed by experiments involving Abx treatment and FMT. Using untargeted metabolomic profiling and 16S rRNA sequencing, we discovered that the level of the secondary bile acid lithocholic acid (LCA) was notably increased and the LCA levels were significantly associated with the abundance of Blautia, Enterorhadus and Rumi-NK4A214_group. Furthermore, LCA exerted anti-inflammatory effects by activating a G-protein-coupled bile acid receptor (TGR5), which inhibited the polarization of classically activated (M1) macrophages. Together, these data suggest that insulin alters the gut microbiota and affects LCA production, ultimately delaying the progression of IBD.