dc.contributorUniversidade Federal de Uberlândia (UFU)
dc.contributorUniv Franca
dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniv Luterana Brasil
dc.contributorUniversidade Federal do Rio Grande do Sul (UFRGS)
dc.contributorUniv Estadual Mato Grosso do Sul
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:34:23Z
dc.date.accessioned2022-10-05T17:19:03Z
dc.date.available2014-05-20T15:34:23Z
dc.date.available2022-10-05T17:19:03Z
dc.date.created2014-05-20T15:34:23Z
dc.date.issued2011-06-01
dc.identifierFood and Chemical Toxicology. Oxford: Pergamon-Elsevier B.V. Ltd, v. 49, n. 6, p. 1235-1241, 2011.
dc.identifier0278-6915
dc.identifierhttp://hdl.handle.net/11449/42534
dc.identifier10.1016/j.fct.2011.03.001
dc.identifierWOS:000291514800007
dc.identifierWOS000291514800007.pdf
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3913391
dc.description.abstractThe dibenzylbutyrolactolic lignan (-)-cubebin was isolated from dry seeds of Piper cubeba L (Piperaceae). (-)-Cubebin possesses anti-inflammatory, analgesic and antimicrobial activities. Doxorubicin (DXR) is a topoisomerase-interactive agent that may induce single- and double-strand breaks, intercalate into the DNA and generate oxygen free radicals. Here, we examine the mutagenicity and recombinogenicity of different concentrations of (-)-cubebin alone or in combination with DXR using standard (ST) and high bioactivation (HB) crosses of the wing Somatic Mutation and Recombination Test in Drosophila melanogaster. The results from both crosses were rather similar. (-)-Cubebin alone did not induce mutation or recombination. At lower concentrations, (-)-cubebin statistically reduced the frequencies of DXR-induced mutant spots. At higher concentrations, however, (-)-cubebin was found to potentiate the effects of DXR, leading to either an increase in the production of mutant spots or a reduction, due to toxicity. These results suggest that depending on the concentration, (-)-cubebin may interact with the enzymatic system that catalyzes the metabolic detoxification of DXR, inhibiting the activity of mitochondria! complex 1 and thereby scavenging free radicals. Recombination was found to be the major effect of the treatments with DXR alone. The combined treatments reduced DXR mutagenicity but did not affect DXR recombinogenicity. (C) 2011 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherPergamon-Elsevier B.V. Ltd
dc.relationFood and Chemical Toxicology
dc.relation3.977
dc.relation1,144
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectSomatic Mutation and Recombination Test
dc.subjectSMART
dc.subjectToxicity
dc.subjectCyp6A2
dc.titleThe effect of the dibenzylbutyrolactolic lignan (-)-cubebin on doxorubicin mutagenicity and recombinogenicity in wing somatic cells of Drosophila melanogaster
dc.typeArtigo


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