Quercetin tests negative for genotoxicity in transcriptome analyses of liver and small intestine of mice

Elise F Hoek-van den Hil1, Evert M van Schothorst2, Inge van der Stelt2

  • 1Human and Animal Physiology, Wageningen University, P.O. Box 338, 6700 AH, Wageningen, The Netherlands; Division of Toxicology, Wageningen University, P.O. Box 8000, 6700 EA, Wageningen, The Netherlands; RIKILT Wageningen UR, P.O. Box 230, 6700 AE Wageningen, The Netherlands.

Insights

Quercetin supplementation in mice showed no genotoxicity in liver and small intestine tissues. Transcriptome analysis confirmed no regulation of genotoxicity-related pathways or DNA damage genes.

Area of Science:

  • Biochemistry
  • Toxicology
  • Nutritional Science

Background:

  • Quercetin is a dietary flavonoid with positive in vitro genotoxicity results.
  • High intake of quercetin via food supplements necessitates in vivo genotoxicity testing.

Purpose of the Study:

  • To evaluate the in vivo genotoxic properties of quercetin in mice.
  • To investigate quercetin's effects on liver and small intestine tissues.

Main Methods:

  • Mice were fed a high-fat diet supplemented with 0.33% quercetin for 12 weeks.
  • Transcriptome analyses (microarray) were performed on liver and small intestine tissues.
  • Serum liver enzymes (ALT, AST) were analyzed for hepatotoxicity indicators.

Main Results:

  • No indications of hepatotoxicity were observed based on serum enzyme levels.
  • Microarray analysis revealed no regulation of genotoxicity-related pathways in liver or small intestine.
  • Analysis of DNA damage genes and a transcriptomic classifier set did not indicate genotoxicity.

Conclusions:

  • Quercetin supplementation at ~350 mg/kg body weight/day for 12 weeks did not induce genotoxicity in mouse liver and small intestine.
  • Transcriptome data provided a weight of evidence against quercetin's in vivo genotoxic potential.