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Sodium ascorbate kills Candida albicans in vitro via iron-catalyzed Fenton reaction: Importance of oxygenation and metabolism

dc.contributor.authorAvci, Pinar
dc.contributor.authorFreire, Fernanda [UNESP]
dc.contributor.authorBanvolgyi, Andras
dc.contributor.authorMylonakis, Eleftherios
dc.contributor.authorWikonkal, Norbert M.
dc.contributor.authorHamblin, Michael R.
dc.contributor.institutionMassachusetts General Hospital
dc.contributor.institutionHarvard Medical School
dc.contributor.institutionSemmelweis University
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionRhode Island Hospital
dc.contributor.institutionHarvard-MIT Division of Health Sciences and Technology
dc.date.accessioned2018-12-11T16:44:48Z
dc.date.available2018-12-11T16:44:48Z
dc.date.issued2016-12-01
dc.description.abstractAim: Ascorbate can inhibit growth and even decrease viability of various microbial species including Candida albicans. However the optimum conditions and the mechanism of action are unclear. Materials/methodology: Candida albicans shaken for 90 min in a buffered solution of ascorbate (90 mM) gave a 5-log reduction of cell viability, while there was no killing without shaking, in growth media with different carbon sources or at 4°C. Killing was inhibited by the iron chelator 2,2′-bipyridyl. Hydroxyphenyl fluorescein probe showed the intracellular generation of hydroxyl radicals. Results/conclusion: Ascorbate-mediated killing of C. albicans depends on oxygenation and metabolism, involves iron-catalyzed generation of hydroxyl radicals via Fenton reaction and depletion of intracellular NADH. Ascorbate could serve as a component of a topical antifungal therapy.en
dc.description.affiliationWellman Center for Photomedicine Massachusetts General Hospital
dc.description.affiliationDepartment of Dermatology Harvard Medical School
dc.description.affiliationDepartment of Dermatology Venerology and Dermato-Oncology Semmelweis University
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP)
dc.description.affiliationInfectious Diseases Division Warren Alpert Medical School of Brown University Rhode Island Hospital
dc.description.affiliationHarvard-MIT Division of Health Sciences and Technology
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP)
dc.format.extent1535-1547
dc.identifierhttp://dx.doi.org/10.2217/fmb-2016-0063
dc.identifier.citationFuture Microbiology, v. 11, n. 12, p. 1535-1547, 2016.
dc.identifier.doi10.2217/fmb-2016-0063
dc.identifier.issn1746-0921
dc.identifier.issn1746-0913
dc.identifier.scopus2-s2.0-84998704947
dc.identifier.urihttp://hdl.handle.net/11449/169180
dc.language.isoeng
dc.relation.ispartofFuture Microbiology
dc.relation.ispartofsjr1,270
dc.relation.ispartofsjr1,270
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectascorbate
dc.subjectCandida albicans
dc.subjecthydroxyl radicals
dc.subjectoxidative stress
dc.subjectvitamin C
dc.titleSodium ascorbate kills Candida albicans in vitro via iron-catalyzed Fenton reaction: Importance of oxygenation and metabolismen
dc.typeArtigo
dspace.entity.typePublication

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