Indoxyl sulfate explained

Indoxyl sulfate, also known as 3-indoxylsulfate and 3-indoxylsulfuric acid, is a metabolite of dietary that acts as a cardiotoxin and uremic toxin. High concentrations of indoxyl sulfate in blood plasma are known to be associated with the development and progression of chronic kidney disease and vascular disease in humans.[1] [2] As a uremic toxin, it stimulates glomerular sclerosis and renal interstitial fibrosis.

Biosynthesis

Indoxyl sulfate is a metabolite of dietary that is synthesized through the following metabolic pathway:

indoleindoxyl → indoxyl sulfate

Indole is produced from in the human intestine via tryptophanase-expressing gastrointestinal bacteria. Indoxyl is produced from indole via enzyme-mediated hydroxylation in the liver; in vitro experiments with rat and human liver microsomes suggest that the CYP450 enzyme CYP2E1 hydroxylates indole into indoxyl.[3] Subsequently, indoxyl is converted into indoxyl sulfate by sulfotransferase enzymes in the liver; based upon in vitro experiments with recombinant human sulfotransferases, SULT1A1 appears to be the primary sulfotransferase enzyme involved in the conversion of indoxyl into indoxyl sulfate.[4]

Clinical significance

Occasionally in urinary tract infections, bacteria produce indoxyl phosphatase which splits indoxyl sulfate forming indigo and indirubin creating dramatic purple urine.[5] Indoxyl sulfate is also a product of indole metabolism, which is produced from tryptophan by intestinal flora, such as Escherichia coli.[6]

Notes and References

  1. Encyclopedia: Indoxyl sulfate . Human Metabolome Database – Version 4.0 . 15 November 2017 . 23 October 2017 .
  2. Encyclopedia: Indoxyl sulfate . PubChem Compound . United States National Library of Medicine – National Center for Biotechnology Information . 15 November 2017 . 11 November 2017.
  3. Banoglu E, Jha GG, King RS . Hepatic microsomal metabolism of indole to indoxyl, a precursor of indoxyl sulfate . European Journal of Drug Metabolism and Pharmacokinetics . 26 . 4 . 235–40 . 2001 . 11808865 . 2254176 . 10.1007/bf03226377.
  4. Banoglu E, King RS . Sulfation of indoxyl by human and rat aryl (phenol) sulfotransferases to form indoxyl sulfate . European Journal of Drug Metabolism and Pharmacokinetics . 27 . 2 . 135–40 . 2002 . 12064372 . 2254172 . 10.1007/bf03190428.
  5. Tan . CK . Wu YP . Wu HY . Lai CC . Purple urine bag syndrome . Canadian Medical Association Journal . 179 . 5 . 491 . August 2008 . 18725621 . 10.1503/cmaj.071604 . 2518199 .
  6. Evenepoel . P . Meijers . BK . Bammens . BR . Verbeke . K . Uremic toxins originating from colonic microbial metabolism. . Kidney International Supplements . December 2009 . 76 . 114 . S12-9 . 10.1038/ki.2009.402 . 19946322. free .