Related Experiment Video
Updated: Apr 15, 2026

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
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.
Abstract:
Given the positive results of quercetin in in vitro genotoxicity studies, the in vivo genotoxic properties of this important dietary flavonoid warrant testing, especially considering possible high intake via widely available food supplements. Here, this was done by transcriptome analyses of the most relevant tissues, liver and small intestine, of quercetin supplemented mice. Quercetin (0.33%) supplemented to a high-fat diet was administered to mice during 12 weeks. Serum alanine aminotransferase and aspartate aminotransferase levels revealed no indications for hepatotoxicity. Microarray pathway analysis of liver and small intestine showed no regulation of genotoxicity related pathways. Analysis of DNA damage related genes also did not point at genotoxicity. Furthermore, a published classifier set of transcripts for identifying genotoxic compounds did not indicate genotoxicity. Only two transcripts of the classifier set were regulated, but in the opposite direction compared with the genotoxic compounds 2-acetylaminofluorene (2-AAF) and aflatoxin B1 (AFB1). Based on the weight of evidence of three different types of analysis, we conclude that supplementation with quercetin at ~350 mg/kg bw/day for 12 weeks in mice showed no up-regulation of genotoxicity related pathways in liver and small intestine.
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.
Related Concept Videos
Mutagenicity and Carcinogenicity
In vitro Mutagenesis

