Population nutrikinetics of green tea extract

PLoS One. 2018 Feb 21;13(2):e0193074. doi: 10.1371/journal.pone.0193074. eCollection 2018.

Abstract

Green tea polyphenols may contribute to the prevention of cancer and other diseases. To learn more about the pharmacokinetics and interindividual variation of green tea polyphenols after oral intake in humans we performed a population nutrikinetic study of standardized green tea extract. 84 healthy participants took green tea extract capsules standardized to 150 mg epigallocatechin-gallate (EGCG) twice a day for 5 days. On day 5 catechin plasma concentrations were analyzed using non-compartmental and population pharmacokinetic methods. A strong between-subject variability in catechin pharmacokinetics was found with maximum plasma concentrations varying more than 6-fold. The AUCs of EGCG, EGC and ECG were 877.9 (360.8-1576.5), 35.1 (8.0-87.4), and 183.6 (55.5-364.6) h*μg/L respectively, and the elimination half lives were 2.6 (1.8-3.8), 3.9 (0.9-10.7) and 1.8 (0.8-2.9) h, respectively. Genetic polymorphisms in genes of the drug transporters MRP2 and OATP1B1 could at least partly explain the high variability in pharmacokinetic parameters. The observed variability in catechin plasma levels might contribute to interindividual variation in benefical and adverse effects of green tea polyphenols. Our data could help to gain a better understanding of the causes of variability of green tea effects and to improve the design of studies on the effects of green tea polyphenols in different health conditions.

Trial registration: ClinicalTrials.gov: NCT01360320.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Catechin / analogs & derivatives*
  • Catechin / chemistry
  • Catechin / pharmacokinetics
  • Catechin / pharmacology
  • Female
  • Humans
  • Male
  • Multidrug Resistance-Associated Protein 2
  • Multidrug Resistance-Associated Proteins / genetics*
  • Multidrug Resistance-Associated Proteins / metabolism
  • Organic Anion Transporters / genetics*
  • Organic Anion Transporters / metabolism
  • Pharmacogenomic Testing*
  • Plant Extracts* / chemistry
  • Plant Extracts* / pharmacokinetics
  • Plant Extracts* / pharmacology
  • Polymorphism, Genetic*
  • Polyphenols* / chemistry
  • Polyphenols* / pharmacokinetics
  • Polyphenols* / pharmacology
  • Tea / chemistry*

Substances

  • ABCC2 protein, human
  • Multidrug Resistance-Associated Protein 2
  • Multidrug Resistance-Associated Proteins
  • Organic Anion Transporters
  • Plant Extracts
  • Polyphenols
  • SLCO1A2 protein, human
  • Tea
  • Catechin
  • epigallocatechin gallate

Associated data

  • ClinicalTrials.gov/NCT01360320

Grants and funding

This pharmacokinetic study was conducted within the Miracle study supported by the German Cancer Aid, Grand No.109133. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.