Acrylamide and glycidamide: genotoxic effects in V79-cells and human blood |
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Authors: | Matthias Baum Evelyne Fauth Silke Fritzen Armin Herrmann Peter Mertes Karlheinz Merz Melanie Rudolphi Heinrich Zankl Gerhard Eisenbrand |
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Affiliation: | aDivision of Food Chemistry and Environmental Toxicology, Department of Chemistry, University of Kaiserslautern, D-67663 Kaiserslautern, Germany;bDivision of Human Genetics, Department of Biology, University of Kaiserslautern, D-67663 Kaiserslautern, Germany |
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Abstract: | Acrylamide (AA) can be formed in certain foods by heating, predominantly from the precursor asparagine. It is a carcinogen in animal experiments, but the relevance of dietary exposure for humans is still under debate. There is substantial evidence that glycidamide (GA), metabolically formed from AA by Cyp 2E1-mediated epoxidation, acts as ultimate mutagenic agent. We compared the mutagenic potential of AA and GA in V79-cells, using the hprt mutagenicity-test with N-methyl-N′-nitro-N-nitroso-guanidine (MNNG) as positive control. Whereas MNNG showed marked mutagenic effectivity already at 0.5 μM, AA was inactive up to a concentration of 10 mM. In contrast, GA showed a concentration dependent induction of mutations at concentrations of 800 μM and higher. Human blood was used as model system to investigate genotoxic potential in lymphocytes by single cell gel electrophoresis (comet assay) and by measuring the induction of micronuclei (MN) with bleomycin (BL) as positive control. AA did not induce significant genotoxicity or mutagenicity up to 6000 μM. With GA, concentration dependent DNA damage was observed in the dose range of 300–3000 μM after 4 h incubation. Significant MN-induction was not observed with AA (up to 5000 μM) and GA (up to 1000 μM), whereas BL (4 μM) induced significantly enhanced MN frequencies. Thus, in our systems GA appears to exert a rather moderate genotoxic activity. |
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Keywords: | Acrylamide Glycidamide Genotoxicity Mutagenicity V79 cells hprt-test Comet assay Micronucleus induction |
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