dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversity of Trás-os-Montes and Alto Douro
dc.date.accessioned2019-10-06T15:37:17Z
dc.date.accessioned2022-12-19T18:31:23Z
dc.date.available2019-10-06T15:37:17Z
dc.date.available2022-12-19T18:31:23Z
dc.date.created2019-10-06T15:37:17Z
dc.date.issued2019-01-01
dc.identifierDrug and Chemical Toxicology.
dc.identifier1525-6014
dc.identifier0148-0545
dc.identifierhttp://hdl.handle.net/11449/187475
dc.identifier10.1080/01480545.2019.1585445
dc.identifier2-s2.0-85063132170
dc.identifier3814504901386844
dc.identifier0000-0002-8645-3777
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5368513
dc.description.abstractCitral, 3,7-dimethyl-2,6-octadien-1-al, one of the main components of the essential oils obtained from several plants, is used as a food additive and as a fragrance for detergents, cosmetics and other toiletries. The literature shows disparity regarding citral genotoxicity. Thus, the main objective of our work was to evaluate the genotoxic effects of citral in human cell cultures, HepG2 and leukocytes. Cytotoxicity assays (trypan blue and MTT) showed citral toxic effects in HepG2 cells (with metabolizing liver enzymes), which contrasted with the absence of toxicity in leukocytes. After citral exposure, both cell types did not demonstrate clastogenic/aneugenic effects in the micronucleus test. However, for the comet assay, citral exposure lead to significant genotoxic effects in both HepG2 (even to citral low concentrations) and leukocytes. The use of citral must be viewed with caution due to its ability to induce DNA damages, especially after being metabolized by cells with active liver enzymes.
dc.languageeng
dc.relationDrug and Chemical Toxicology
dc.rightsAcesso aberto
dc.sourceScopus
dc.subject3,7-dimethyl-2,6 octadienal
dc.subjectcomet assay
dc.subjectmicronucleus test
dc.subjectMTT assay
dc.titleCitral presents cytotoxic and genotoxic effects in human cultured cells
dc.typeArtículos de revistas


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