Nonmutagenicity in vivo of the food flavonol quercetin
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Nutrition and Cancer
|January 1, 1982
Abstract:
Mice given quercetin per os at concentrations that were about 10(3) times greater than the estimated average human intake of total flavonols were tested for mutagenicity with 2 complementary in vivo mutagenicity/carcinogenicity screening tests--the micronucleus test and the host-mediated assay employing the Ames Salmonella tester strain TA 98 as indicator organism. No mutagenic effect was detected with either test.
Insights
Quercetin, a common flavonol, was tested for mutagenicity in mice at high doses. Studies found no evidence of mutagenic effects, suggesting safety at elevated dietary levels.
Area of Science:
- Toxicology
- Nutritional Science
- Genetics
Background:
- Quercetin is a prevalent dietary flavonol found in many fruits and vegetables.
- Understanding the in vivo mutagenicity of quercetin is crucial for assessing its safety profile.
Purpose of the Study:
- To evaluate the potential mutagenic effects of quercetin administered at high doses in a mammalian model.
- To assess the genotoxicity of quercetin using complementary in vivo assays.
Main Methods:
- Mice were administered quercetin orally at concentrations significantly exceeding estimated human intake.
- Mutagenicity was assessed using two established in vivo screening tests: the micronucleus test and the host-mediated assay.
- The Ames Salmonella tester strain TA 98 was used as the indicator organism in the host-mediated assay.
Main Results:
- No mutagenic effects were observed in the micronucleus test.
- The host-mediated assay also revealed no mutagenic activity of quercetin.
- Quercetin did not induce genetic mutations under the tested in vivo conditions.
Conclusions:
- High-dose oral administration of quercetin did not demonstrate mutagenicity in mice.
- The findings suggest that quercetin is not genotoxic in vivo at the tested concentrations.
- Further research can explore the long-term safety and potential benefits of quercetin supplementation.