DSS-induced colitis activates the kynurenine pathway in serum and brain by affecting IDO-1 and gut microbiota

Front Immunol. 2023 Jan 26:13:1089200. doi: 10.3389/fimmu.2022.1089200. eCollection 2022.

Abstract

Accumulative studies suggest that inflammatory bowel disease (IBD) may cause multiple central nervous system (CNS) pathologies. Studies have found that indoleamine-2,3-dioxygenase (IDO, rate-limiting enzyme of the kynurenine (Kyn) pathway) deficient mice were protected from endotoxin induced cognitive impairment, and Kyn administration induced cognitive memory deficits in both control and IDO-deficient mice. However, there is no investigation of the brain Kyn pathway in IBD, thus we investigated whether dextran sulfate sodium (DSS)-induced colitis could cause dysregulation of Kyn pathway in brain, and also in serum. C57BL/6J mice were given drinking water with 2% DSS for 10 consecutive days to induce colitis. In serum, we found significant increase in Kyn and kynurenic acid (Kyna) level, which was regulated by IDO-1 and KAT2 (rate-limiting enzymes of Trp-Kyn-Kyna pathway). Similarly, by analyzing GEO datasets, higher IDO-1 levels in peripheral blood monocytes and colon of UC patients was found. Furthermore, the Kyn pathway was significantly upregulated in the cerebral cortex under the action of IDO-1 after DSS treatment, which ultimately induced the neurotoxic phenotype of astrocytes. To investigate whether gut microbiota is involved in IBD-induced Kyn pathway dysregulation, we performed intestinal flora 16S rRNA sequencing and found that DSS-induced colitis significantly altered the composition and diversity of the gut microbiota. Metabolic function analysis also showed that Tryptophan metabolism, NOD-like receptor signaling pathway and MAPK signaling pathway were significantly up-regulated in the 2% DSS group. A significant association between intestinal flora and Trp metabolism (both in serum and brain) was found by correlation analysis. Overall, this study revealed that DSS-induced colitis causes dysregulation of the Kyn pathway in serum and brain by affecting rate-limiting enzymes and intestinal flora.

Keywords: DSS-induced colitis; gut microbiota; indoleamine-2,3-dioxygenase (IDO); kynurenine pathway (KP); tryptophan metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism
  • Colitis* / metabolism
  • Gastrointestinal Microbiome*
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism
  • Inflammatory Bowel Diseases*
  • Kynurenine / metabolism
  • Mice
  • Mice, Inbred C57BL
  • RNA, Ribosomal, 16S
  • Tryptophan / metabolism
  • Tryptophan Oxygenase / metabolism

Substances

  • Kynurenine
  • Tryptophan
  • RNA, Ribosomal, 16S
  • Tryptophan Oxygenase
  • Indoleamine-Pyrrole 2,3,-Dioxygenase

Grants and funding

This study was supported by Grants from The National Natural Science Foundation of China (81771384 and 82171429 to Y-QS), Public Health Research Center at Jiangnan University (JUPH201801 to Y-QS), and National First-Class Discipline Program of Food Science and Technology (JUFSTR20180101 to Y-QS), Wuxi Municipal Health Commission (1286010241190480 to Y-QS).