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Apocynin: Chemical and biophysical properties of a NADPH oxidase inhibitor

dc.contributor.authorPetrônio, Maicon S. [UNESP]
dc.contributor.authorZeraik, Maria Luiza [UNESP]
dc.contributor.authorDa Fonseca, Luiz Marcos [UNESP]
dc.contributor.authorXimenes, Valdecir F. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:28:37Z
dc.date.available2014-05-27T11:28:37Z
dc.date.issued2013-03-01
dc.description.abstractApocynin is the most employed inhibitor of NADPH oxidase (NOX), a multienzymatic complex capable of catalyzing the one-electron reduction of molecular oxygen to the superoxide anion. Despite controversies about its selectivity, apocynin has been used as one of the most promising drugs in experimental models of inflammatory and neurodegenerative diseases. Here, we aimed to study the chemical and biophysical properties of apocynin. The oxidation potential was determined by cyclic voltammetry (Epa = 0.76V), the hydrophobicity index was calculated (logP = 0.83) and the molar absorption coefficient was determined (ε275nm = 1.1 × 104 M-1 cm-1). Apocynin was a weak free radical scavenger (as measured using the DPPH, peroxyl radical and nitric oxide assays) when compared to protocatechuic acid, used here as a reference antioxidant. On the other hand, apocynin was more effective than protocatechuic acid as scavenger of the non-radical species hypochlorous acid. Apocynin reacted promptly with the non-radical reactive species H2O2 only in the presence of peroxidase. This finding is relevant, since it represents a new pathway for depleting H2O2 in cellular experimental models, besides the direct inhibition of NADPH oxidase. This could be relevant for its application as an inhibitor of NOX4, since this isoform produces H 2O2 and not superoxide anion. The binding parameters calculated by fluorescence quenching showed that apocynin binds to human serum albumin (HSA) with a binding affinity of 2.19 × 104 M -1. The association did not alter the secondary and tertiary structure of HSA, as verified by synchronous fluorescence and circular dichroism. The displacement of fluorescent probes suggested that apocynin binds to site I and site II of HSA. Considering the current biomedical applications of this phytochemical, the dissemination of these chemical and biophysical properties can be very helpful for scientists and physicians interested in the use of apocynin.en
dc.description.affiliationDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Unesp-Univ Estadual Paulista, Araraquara, SP 14801-902
dc.description.affiliationDepartamento de Química Orgânica Instituto de Química Unesp-Univ Estadual Paulista, Araraquara, SP, 14800-900
dc.description.affiliationDepartamento de Química Faculdade de Ciências Unesp-Univ Estadual Paulista, Bauru, SP 17033-360
dc.description.affiliationUnespDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Unesp-Univ Estadual Paulista, Araraquara, SP 14801-902
dc.description.affiliationUnespDepartamento de Química Orgânica Instituto de Química Unesp-Univ Estadual Paulista, Araraquara, SP, 14800-900
dc.description.affiliationUnespDepartamento de Química Faculdade de Ciências Unesp-Univ Estadual Paulista, Bauru, SP 17033-360
dc.format.extent2821-2839
dc.identifierhttp://dx.doi.org/10.3390/molecules18032821
dc.identifier.citationMolecules, v. 18, n. 3, p. 2821-2839, 2013.
dc.identifier.doi10.3390/molecules18032821
dc.identifier.file2-s2.0-84875625176.pdf
dc.identifier.issn1420-3049
dc.identifier.scopus2-s2.0-84875625176
dc.identifier.urihttp://hdl.handle.net/11449/74759
dc.identifier.wosWOS:000316611700028
dc.language.isoeng
dc.relation.ispartofMolecules
dc.relation.ispartofjcr3.098
dc.relation.ispartofsjr0,855
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAlbumin
dc.subjectApocynin
dc.subjectBinding constant
dc.subjectHydrogen peroxide
dc.subjectNADPH oxidase
dc.subjectacetophenone derivative
dc.subjectapocynin
dc.subjectenzyme inhibitor
dc.subjecthydrogen peroxide
dc.subjecthypochlorous acid
dc.subjectreduced nicotinamide adenine dinucleotide phosphate oxidase
dc.subjectscavenger
dc.subjectchemical phenomena
dc.subjectchemistry
dc.subjectdrug antagonism
dc.subjectkinetics
dc.subjectoxidation reduction reaction
dc.subjectpH
dc.subjectAcetophenones
dc.subjectEnzyme Inhibitors
dc.subjectFree Radical Scavengers
dc.subjectHydrogen Peroxide
dc.subjectHydrogen-Ion Concentration
dc.subjectHydrophobic and Hydrophilic Interactions
dc.subjectHypochlorous Acid
dc.subjectKinetics
dc.subjectNADPH Oxidase
dc.subjectOxidation-Reduction
dc.titleApocynin: Chemical and biophysical properties of a NADPH oxidase inhibitoren
dc.typeArtigopt
dcterms.licensehttp://www.mdpi.com/about/openaccess
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências, Baurupt
unesp.departmentQuímica - FCpt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentQuímica Orgânica - IQARpt

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