Chemistry:Urolithin

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Short description: Group of chemical compounds
Chemical structure of urolithin A.

Urolithins are microflora metabolites of dietary ellagic acid derivatives, such as ellagitannins.[1] They are produced in the gut, and found in the urine in the form of urolithin B glucuronide after absorption of ellagitannins-containing foods, such as pomegranate.[2] During intestinal metabolism by bacteria, ellagitannins and punicalagins are converted to urolithins, which have unknown biological activity in vivo.

Ellagitannins exhibit low bioavailability and are transformed in the gut to ellagic acid and its microbiota metabolites. Urolithins are found in plasma mostly as glucuronides at low concentrations.[3] Urolithins production is dependent on the gut microbiome enterotype. Individuals producing urolithins show a much higher abundance of the Clostridium leptum group of Firmicutes phylum than Bacteroides or Prevotella.[4]

Known molecules

  • Urolithin A (3,8-Dihydroxyurolithin)
  • Urolithin A glucuronide
  • Urolithin B (3-Hydroxyurolithin)
  • urolithin B glucuronide
  • Urolithin D (3,4,8,9-Tetrahydroxyurolithin)

catabolic intermediates:

  • Urolithin M-5
  • Urolithin M-6
  • Urolithin M-7
  • Urolithin C (3,8,9-Trihydroxy urolithin)
  • Urolithin E (2,3,8,10-Tetrahydroxy urolithin)

See also

  • Pomegranate ellagitannins

References

  1. Larrosa, M; González-Sarrías, A; García-Conesa, MT; Tomás-Barberán, FA; Espín, JC (2006). "Urolithins, ellagic acid-derived metabolites produced by human colonic microflora, exhibit estrogenic and antiestrogenic activities". Journal of Agricultural and Food Chemistry 54 (5): 1611–1620. doi:10.1021/jf0527403. PMID 16506809. 
  2. "Urolithins, intestinal microbial metabolites of Pomegranate ellagitannins, exhibit potent antioxidant activity in a cell-based assay". J Agric Food Chem 57 (21): 10181–6. 11 November 2009. doi:10.1021/jf9025794. PMID 19824638. 
  3. Giménez-Bastida, Juan A.; González-Sarrías, Antonio; Larrosa, Mar; Tomás-Barberán, Francisco; Espín, Juan C.; García-Conesa, María-Teresa (2012). "Ellagitannin metabolites, urolithin a glucuronide and its aglycone urolithin A, ameliorate TNF-α-induced inflammation and associated molecular markers in human aortic endothelial cells". Molecular Nutrition & Food Research 56 (5): 784–796. doi:10.1002/mnfr.201100677. PMID 22648625. 
  4. García-Villalba, Rocío; Beltrán, David; Espín, Juan Carlos; Selma, María Victoria; Tomás-Barberán, Francisco A. (2013). "Time Course Production of Urolithins from Ellagic Acid by Human Gut Microbiota". Journal of Agricultural and Food Chemistry 61 (37): 8797–8806. doi:10.1021/jf402498b. PMID 23984796.