Structural identification of two metabolites of catechins and their kinetics in human urine and blood after tea ingestion
- PMID: 10725114
- DOI: 10.1021/tx9901837
Structural identification of two metabolites of catechins and their kinetics in human urine and blood after tea ingestion
Abstract
Tea is a popular beverage consumed worldwide. The metabolic fate of its major constituents, catechins, however, is not well-known. In this study, two catechin metabolites were detected in the urine and plasma of human volunteers after ingestion of green tea. These metabolites were identified by LC/ESI-MS and NMR as (-)-5-(3',4', 5'-trihydroxyphenyl)-gamma-valerolactone (M4) and (-)-5-(3', 4'-dihydroxyphenyl)-gamma-valerolactone (M6). The renal excretion of M4 and M6 had a 3 h lag time and peaked 7.5-13.5 h after ingestion of a single dose of green tea, while (-)-epigallocatechin (EGC) and (-)-epicatechin peaked at 2 h. M4 and M6 were two major tea metabolites with urinary cumulative excretions as high as 8-25 times the levels of EGC and (-)-epicatechin in some of our subjects, and accounted for 6-39% of the amounts of ingested EGC and (-)-epicatechin. Both the metabolites appeared to be produced by intestinal microorganisms, with EGC and (-)-epicatechin as the precursors of M4 and M6, respectively. Repeated ingestion of green tea produced a slight accumulative effect of the metabolites. They were also detected in the plasma, exhibiting kinetics similar to those of the urinary metabolites, and in the feces. Study on these metabolites may help us further understand the cancer chemopreventive actions and other beneficial effects of tea.
Similar articles
-
Identification and characterization of methylated and ring-fission metabolites of tea catechins formed in humans, mice, and rats.Chem Res Toxicol. 2002 Aug;15(8):1042-50. doi: 10.1021/tx010184a. Chem Res Toxicol. 2002. PMID: 12184788
-
Pharmacokinetics of tea catechins after ingestion of green tea and (-)-epigallocatechin-3-gallate by humans: formation of different metabolites and individual variability.Cancer Epidemiol Biomarkers Prev. 2002 Oct;11(10 Pt 1):1025-32. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 12376503
-
Analysis of urinary metabolites of tea catechins by liquid chromatography/electrospray ionization mass spectrometry.Chem Res Toxicol. 2001 Jun;14(6):702-7. doi: 10.1021/tx0002536. Chem Res Toxicol. 2001. PMID: 11409941
-
Absorption, metabolism, distribution and excretion of (-)-epicatechin: A review of recent findings.Mol Aspects Med. 2018 Jun;61:18-30. doi: 10.1016/j.mam.2017.11.002. Epub 2017 Nov 9. Mol Aspects Med. 2018. PMID: 29126853 Review.
-
Inhibitory Effects of Eight Green Tea Catechins on Cytochrome P450 1A2, 2C9, 2D6, and 3A4 Activities.J Pharm Pharm Sci. 2016 Apr-Jun;19(2):188-97. doi: 10.18433/J3MS5C. J Pharm Pharm Sci. 2016. PMID: 27518169 Review.
Cited by
-
Flavanols and anthocyanins in cardiovascular health: a review of current evidence.Int J Mol Sci. 2010 Apr 13;11(4):1679-703. doi: 10.3390/ijms11041679. Int J Mol Sci. 2010. PMID: 20480037 Free PMC article. Review.
-
Effect of 2-month controlled green tea intervention on lipoprotein cholesterol, glucose, and hormone levels in healthy postmenopausal women.Cancer Prev Res (Phila). 2012 Mar;5(3):393-402. doi: 10.1158/1940-6207.CAPR-11-0407. Epub 2012 Jan 13. Cancer Prev Res (Phila). 2012. PMID: 22246619 Free PMC article. Clinical Trial.
-
Potential Therapeutic Targets of Epigallocatechin Gallate (EGCG), the Most Abundant Catechin in Green Tea, and Its Role in the Therapy of Various Types of Cancer.Molecules. 2020 Jul 9;25(14):3146. doi: 10.3390/molecules25143146. Molecules. 2020. PMID: 32660101 Free PMC article. Review.
-
Immunomodulatory Effects of Green Tea Catechins and Their Ring Fission Metabolites in a Tumor Microenvironment Perspective.Molecules. 2024 Sep 26;29(19):4575. doi: 10.3390/molecules29194575. Molecules. 2024. PMID: 39407505 Free PMC article. Review.
-
Wine polyphenols: potential agents in neuroprotection.Oxid Med Cell Longev. 2012;2012:805762. doi: 10.1155/2012/805762. Epub 2012 Jul 5. Oxid Med Cell Longev. 2012. PMID: 22829964 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources