dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:21:56Z
dc.date.accessioned2022-10-05T18:02:29Z
dc.date.available2014-05-27T11:21:56Z
dc.date.available2022-10-05T18:02:29Z
dc.date.created2014-05-27T11:21:56Z
dc.date.issued2006-08-01
dc.identifierOral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, v. 102, n. 2, 2006.
dc.identifier1079-2104
dc.identifierhttp://hdl.handle.net/11449/69015
dc.identifier10.1016/j.tripleo.2005.11.026
dc.identifier2-s2.0-33746363812
dc.identifier5051118752980903
dc.identifier7528116925519142
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3918514
dc.description.abstractObjective: To investigate if formocresol, paramonochlorophenol, or calcium hydroxide modulate the genotoxic effects induced by the oxidatively damaging agent hydrogen peroxide (H 2O 2) or the alkylating agent methyl methanesulfonate (MMS) in vitro by using single cell gel (comet) assay. Study design: Chinese hamster ovary (CHO) cells in culture were exposed directly to formocresol, paramonochlorophenol, or calcium hydroxide (adjusted to 100 μg/mL) for 1 hour at 37°C. Subsequently the cultures were incubated with increasing concentrations (0-10 μmol/L) of MMS in phosphate-buffered solution (PBS) for 15 minutes at 37°C or of H 2O 2 at increasing concentrations (0-100 μmol/L) in distilled water for 5 minutes on ice. The negative control cells were treated with PBS for 1 hour at 37°C. The parameter from the comet assay (tail moment) was assessed by the Kruskal-Wallis nonparametric test followed by a post hoc analysis (Dunn test). Results: Clear concentration-related effects were observed for the genotoxin-exposed CHO cells. Increase of MMS-induced DNA damage was not significantly altered by the presence of the compounds tested. Similarly, no significant changes were observed when hydrogen peroxide was used with the endodontic compounds evaluated. Conclusion: Formocresol, paramonochlorophenol, and calcium hydroxide are not able to modulate alkylation-induced genotoxicity or oxidative DNA damage as depicted by the single cell gel (comet) assay. © 2006 Mosby, Inc. All rights reserved.
dc.languageeng
dc.relationOral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology
dc.rightsAcesso restrito
dc.sourceScopus
dc.subject4 chlorophenol
dc.subject4-chlorophenol
dc.subjectalkylating agent
dc.subjectcalcium hydroxide
dc.subjectchlorophenol
dc.subjectformocresol
dc.subjecthydrogen peroxide
dc.subjectmesylic acid methyl ester
dc.subjectoxidizing agent
dc.subjectroot canal filling material
dc.subjecttopical antiinfective agent
dc.subjectanimal
dc.subjectCHO cell
dc.subjectcomet assay
dc.subjectCricetulus
dc.subjectDNA damage
dc.subjectdrug effect
dc.subjecthamster
dc.subjectmutagenesis
dc.subjectnonparametric test
dc.subjectoxidative stress
dc.subjectAlkylating Agents
dc.subjectAnimals
dc.subjectAnti-Infective Agents, Local
dc.subjectCalcium Hydroxide
dc.subjectChlorophenols
dc.subjectCHO Cells
dc.subjectComet Assay
dc.subjectCricetinae
dc.subjectDNA Damage
dc.subjectFormocresols
dc.subjectHydrogen Peroxide
dc.subjectMethyl Methanesulfonate
dc.subjectMutagenesis
dc.subjectOxidants
dc.subjectOxidative Stress
dc.subjectRoot Canal Filling Materials
dc.subjectStatistics, Nonparametric
dc.titleAntimicrobial endodontic compounds do not modulate alkylation-induced genotoxicity and oxidative stress in vitro
dc.typeArtigo


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