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Steady-State pharmacokinetics and tolerability of trans-resveratrol 2000 mg twice daily with food, quercetin and alcohol (ethanol) in healthy human subjects

Charles la Porte, Nha Voduc, Guijun Zhang, Isabelle Seguin, Danielle Tardiff, Neera Singhal, D William Cameron
Clinical pharmacokinetics 2010 49(7):449

Bibliography

PubMed
PMID 20528005
Funding
Funding was not specified in the indexed record or the disclosure metadata available for this entry.
Competing interests
A competing-interest declaration was not available in the indexed record or the disclosure metadata used for this entry.

Study snapshot

DesignOpen-label within-subject steady-state pharmacokinetic study
ModelHuman intervention research
Sample8 healthy adults
InterventionTrans-resveratrol 2,000 mg twice daily under food, alcohol, and quercetin 500 mg twice-daily conditions
DurationTwo-period repeated-dose study
EndpointsExposure and pharmacokinetics

What the study showed, in plain terms

Published in 2010, this source examined safety, interactions and special populations. Design: Open-label within-subject steady-state pharmacokinetic study. Sample/model: 8 healthy adults. The exposure or intervention was Trans-resveratrol 2,000 mg twice daily under food, alcohol, and quercetin 500 mg twice-daily conditions. Follow-up or treatment period: Two-period repeated-dose study.

Quercetin did not increase resveratrol exposure; a high-fat breakfast reduced it. Diarrhea was frequent during the high-dose resveratrol study.

Small resveratrol-centered experiment. Adverse effects cannot be assigned to quercetin alone, and this does not establish a general synergy between the compounds.

Continue with Quercetin Data Center

For topic-level interpretation, read Quercetin and Resveratrol Together: Evidence and Practical Choices. This is a related guide; the citation panel separately identifies articles that directly cite this paper.

Key findings

  • Quercetin did not increase resveratrol exposure; a high-fat breakfast reduced it.
  • Diarrhea was frequent during the high-dose resveratrol study.
  • The recorded outcome domains were Exposure and pharmacokinetics.
  • The result applies to the tested exposure: Trans-resveratrol 2,000 mg twice daily under food, alcohol, and quercetin 500 mg twice-daily conditions; Two-period repeated-dose study.

What this study can and cannot tell us

  • Small resveratrol-centered experiment. Adverse effects cannot be assigned to quercetin alone, and this does not establish a general synergy between the compounds.
  • A change in blood exposure or a metabolic marker is not a demonstrated improvement in symptoms, disease events or lifespan. The tested formulation and co-administered medicines matter.
  • Source basis: Source check: PubMed abstract and indexed metadata; full methods were not independently confirmed for this entry. Missing method details, funding information or participant denominators are not inferred.

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