4.7 Article

Novel Regioselective Synthesis of Urolithin Glucuronides-Human Gut Microbiota Cometabolites of Ellagitannins and Ellagic Acid

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 70, Issue 19, Pages 5819-5828

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.2c00170

Keywords

ellagic acid; gut microbiota metabolites; urolithins; glucuronides; synthesis

Funding

  1. Taif University, Saudi Arabia [TURSP-HC2021/3]

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Urolithins are human gut microbiota metabolites produced from ellagic acid. They are better absorbed than ellagic acid and have biological activities that may be responsible for the health effects observed after consuming foods containing ellagitannins and ellagic acid. This study successfully synthesized urolithin glucuronide conjugates and characterized their properties.
Urolithins (dibenzo-pyran-[b,d]-6 one derivatives) are human gut microbiota metabolites produced from the natural food antioxidant ellagic acid. Urolithins are better absorbed than ellagic acid and demonstrate biological activities that suggest that they are responsible for the health effects observed after consuming ellagitannin-and ellagic acid-containing foods. Urolithins occur in the systemic circulation as glucuronide conjugates following phase II metabolism. These phase II conjugates are essential for testing the urolithin mechanisms of action in human cell line bioassays. Urolithin glucuronides are not commercially available, and their biosynthesis leads to mixtures of regional isomers. This study describes a novel and regioselective synthesis of urolithin A (3,8-dihydroxy urolithin) 3- and 8-glucuronides and isourolithin A (3,9-dihydroxy urolithin) 3-and 9-glucuronides. The metabolites were characterized using H-1 and C-13 NMR spectroscopy and UV spectrophotometry. The presence of these metabolites in human subjects belonging to different urolithin metabotypes was also investigated.

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