Quercetin metabolites downregulate cyclooxygenase-2 transcription in human lymphocytes ex vivo but not in vivo

J Nutr. 2004 Mar;134(3):552-7. doi: 10.1093/jn/134.3.552.

Abstract

Flavonoids have the potential to modulate inflammation by inhibition of cyclooxygenase-2 (COX-2) transcription. In this study, we compared the effect of the human flavonoid plasma metabolites (quercetin 3'-sulfate, quercetin 3-glucuronide and 3'-methylquercetin 3-glucuronide) on expression of COX-2 mRNA in human lymphocytes ex vivo using TaqMan real-time RT-PCR. We show that the flavonoid quercetin metabolites as detected in human plasma at physiologically significant concentrations inhibit COX-2 expression in human lymphocytes ex vivo. To examine the effect in vivo, we measured COX-2 mRNA levels in 8 subjects (5 men and 3 women) participating in a 3-way, single-blind, randomized crossover study after consumption of a single meal of white, low-quercetin onions, compared with yellow, high-quercetin onions. After consumption of high-quercetin onions, quercetin conjugates were detected in plasma (up to a maximum concentration of 4 micro mol/L at approximately 1 h). However, the expression of COX-2 mRNA in lymphocytes was unchanged by the consumption of high-quercetin onions compared with the low-quercetin group. The results show that a single high dose of the flavonoid quercetin from onions does not change COX-2 mRNA expression in human lymphocytes in vivo even though this change occurred in vitro and ex vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biotransformation
  • Cyclooxygenase 2
  • DNA Primers
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Isoenzymes / genetics*
  • Kinetics
  • Lymphocytes / drug effects
  • Lymphocytes / enzymology*
  • Membrane Proteins
  • Onions*
  • Prostaglandin-Endoperoxide Synthases / genetics*
  • Quercetin / analogs & derivatives*
  • Quercetin / blood
  • Quercetin / pharmacokinetics
  • Quercetin / pharmacology*
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Time Factors
  • Transcription, Genetic / drug effects*

Substances

  • DNA Primers
  • Isoenzymes
  • Membrane Proteins
  • RNA, Messenger
  • Quercetin
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases