In vivo genotoxicity assessment of acrylamide and glycidyl methacrylate
| Autor: | Vasily N. Dobrovolsky, L. Patrice McDaniel, M. Monserrat Pacheco-Martinez, Wei Ding, Mason G. Pearce |
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| Rok vydání: | 2016 |
| Předmět: |
Male
0301 basic medicine DNA damage Gene mutation Toxicology medicine.disease_cause 03 medical and health sciences Clastogen Reticulocyte medicine Animals Acrylamide Dose-Response Relationship Drug Chemistry General Medicine Molecular biology Rats Comet assay 030104 developmental biology medicine.anatomical_structure Micronucleus test Immunology Epoxy Compounds Methacrylates Comet Assay Bone marrow Genotoxicity Food Science |
| Zdroj: | Food and Chemical Toxicology. 87:120-127 |
| ISSN: | 0278-6915 |
| DOI: | 10.1016/j.fct.2015.12.006 |
| Popis: | Acrylamide (ACR) and glycidyl methacrylate (GMA) are structurally related compounds used for making polymers with various properties. Both chemicals can be present in food either as a byproduct of processing or a constituent of packaging. We performed a comprehensive evaluation of ACR and GMA genotoxicity in Fisher 344 rats using repeated gavage administrations. Clastogenicity was measured by scoring micronucleated (MN) erythrocytes from peripheral blood, DNA damage in liver, bone marrow and kidneys was measured using the Comet assay, and gene mutation was measured using the red blood cell (RBC) and reticulocyte Pig-a assay. A limited histopathology evaluation was performed in order to determine levels of cytotoxicity. Doses of up to 20 mg/kg/day of ACR and up to 250 mg/kg/day of GMA were used. ACR treatment resulted in DNA damage in the liver, but not in the bone marrow. While ACR was not a clastogen, it was a weak (equivocal) mutagen in the cells of bone marrow. GMA caused DNA damage in the cells of bone marrow, liver and kidney, and induced MN reticulocytes and Pig-a mutant RBCs in a dose-dependent manner. Collectively, our data suggest that both compounds are in vivo genotoxins, but the genotoxicity of ACR is tissue specific. |
| Databáze: | OpenAIRE |
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