The gut microbiota metabolite capsiate promotes Gpx4 expression by activating TRPV1 to inhibit intestinal ischemia reperfusion-induced ferroptosis

Gut Microbes. 2021 Jan-Dec;13(1):1-21. doi: 10.1080/19490976.2021.1902719.

Abstract

Ferroptosis, a new type of cell death has been found to aggravate intestinal ischemia/reperfusion (I/R) injury. However, little is known about the changes of gut microbiota and metabolites in intestinal I/R and the role of gut microbiota metabolites on ferroptosis-induced intestinal I/R injury. This study aimed to establish a mouse intestinal I/R model and ileum organoid hypoxia/reoxygenation (H/R) model to explore the changes of the gut microbiota and metabolites during intestinal I/R and protective ability of capsiate (CAT) against ferroptosis-dependent intestinal I/R injury. Intestinal I/R induced disturbance of gut microbiota and significant changes in metabolites. We found that CAT is a metabolite of the gut microbiota and that CAT levels in the preoperative stool of patients undergoing cardiopulmonary bypass were negatively correlated with intestinal I/R injury. Furthermore, CAT reduced ferroptosis-dependent intestinal I/R injury in vivo and in vitro. However, the protective effects of CAT against ferroptosis-dependent intestinal I/R injury were abolished by RSL3, an inhibitor of glutathione peroxidase 4 (Gpx4), which is a negative regulator of ferroptosis. We also found that the ability of CAT to promote Gpx4 expression and inhibit ferroptosis-dependent intestinal I/R injury was abrogated by JNJ-17203212, an antagonist of transient receptor potential cation channel subfamily V member 1 (TRPV1). This study suggests that the gut microbiota metabolite CAT enhances Gpx4 expression and inhibits ferroptosis by activating TRPV1 in intestinal I/R injury, providing a potential avenue for the management of intestinal I/R injury.

Keywords: Gpx4; Intestinal ischemia/reperfusion injury; TRPV1; capsiate; ferroptosis; metabolites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminopyridines / pharmacology
  • Animals
  • Capsaicin / analogs & derivatives*
  • Capsaicin / metabolism
  • Carbolines / pharmacology
  • Cecum / microbiology
  • DNA, Bacterial
  • Disease Models, Animal
  • Feces / chemistry
  • Ferroptosis*
  • Gastrointestinal Microbiome*
  • Gene Expression Regulation
  • Host Microbial Interactions
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phospholipid Hydroperoxide Glutathione Peroxidase / antagonists & inhibitors
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism*
  • Piperazines / pharmacology
  • RNA, Ribosomal, 16S
  • Reperfusion Injury / drug therapy
  • Reperfusion Injury / metabolism*
  • TRPV Cation Channels / antagonists & inhibitors
  • TRPV Cation Channels / metabolism*

Substances

  • 4-(3-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid (5-trifluoromethylpyridin-2-yl)amide
  • Aminopyridines
  • Carbolines
  • DNA, Bacterial
  • Piperazines
  • RNA, Ribosomal, 16S
  • RSL3 compound
  • TRPV Cation Channels
  • TRPV1 protein, mouse
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • capsiate
  • Capsaicin

Grants and funding

This work was supported by grants from National Natural Science Foundation, Beijing, China (81671955 to Kexuan Liu, 82902010 to Jingjuan Hu), Key Program of National Natural Science Foundation, Beijing, China (81730058 to Kexuan Liu); National Natural Science Foundation of China [82902010]; National Natural Science Foundation of China [81730058]; National Natural Science Foundation of China [81671955].