Aryl Hydrocarbon Receptor Activation in Chronic Kidney Disease: Role of Uremic Toxins

Nephron. 2017;137(1):1-7. doi: 10.1159/000476074. Epub 2017 May 11.

Abstract

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor involved in the expression of xenobiotic-metabolizing enzymes, inflammatory cytokines and adhesion molecules. Uremic toxins such as indoxyl sulfate and indole acetic acid are derived from tryptophan fermentation by gut microbiota; they accumulate in patients with chronic kidney disease (CKD) on haemodialysis and have recently emerged as potent ligands of AhR. Therefore, AhR can serve as a mediator in inflammation and cardiovascular diseases in these patients. This review discusses current data that support a link between AhR activation and uremic toxins from gut microbiota in CKD.

Keywords: Aryl hydrocarbon receptor; Chronic kidney disease; Inflammation; Uremic toxins.

Publication types

  • Review

MeSH terms

  • Animals
  • Cardiovascular Diseases / etiology
  • Glucuronates / metabolism
  • Humans
  • Indican / metabolism
  • Indoleacetic Acids / metabolism
  • Indoles / metabolism
  • Models, Biological
  • Receptors, Aryl Hydrocarbon / metabolism*
  • Renal Insufficiency, Chronic / metabolism*
  • Toxins, Biological / metabolism*
  • Tryptophan / metabolism
  • Uremia / metabolism

Substances

  • Glucuronates
  • Indoleacetic Acids
  • Indoles
  • Receptors, Aryl Hydrocarbon
  • Toxins, Biological
  • indoxyl glucuronide
  • indoleacetic acid
  • Tryptophan
  • Indican