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Decavanadate induces mitochondrial membrane depolarization and inhibits oxygen consumption

dc.contributor.authorSoares, Sandra S.
dc.contributor.authorGutiérrez-Merino, Carlos
dc.contributor.authorAureliano, M.
dc.date.accessioned2012-06-26T10:25:14Z
dc.date.available2012-06-26T10:25:14Z
dc.date.issued2007
dc.description.abstractDecavanadate induced rat liver mitochondrial depolarization at very low concentrations, half-depolarization with 39 nM decavanadate, while it was needed a 130-fold higher concentration of monomeric vanadate (5 lM) to induce the same effect. Decavanadate also inhibits mitochondrial repolarization induced by reduced glutathione in vitro, with an inhibition constant of 1 lM, whereas no effect was observed up to 100 lM of monomeric vanadate. The oxygen consumption by mitochondria is also inhibited by lower decavanadate than monomeric vanadate concentrations, i.e. 50% inhibition is attained with 99 nM decavanadate and 10 lM monomeric vanadate. Thus, decavanadate is stronger as mitochondrial depolarization agent than as inhibitor of mitochondrial oxygen consumption. Up to 5 lM, decavanadate does not alter mitochondrial NADH levels nor inhibit neither FOF1-ATPase nor cytochrome c oxidase activity, but it induces changes in the redox steady-state of mitochondrial b-type cytochromes (complex III). NMR spectra showed that decameric vanadate is the predominant vanadate species in decavanadate solutions. It is concluded that decavanadate is much more potent mitochondrial depolarization agent and a more potent inhibitor of mitochondrial oxygen consumption than monomeric vanadate, pointing out the importance to take into account the contribution of higher oligomeric species of vanadium for the biological effects of vanadate solutions.por
dc.identifier.issn0162-0134
dc.identifier.urihttp://hdl.handle.net/10400.1/1297
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.subjectDecavanadatepor
dc.subjectMitochondriapor
dc.titleDecavanadate induces mitochondrial membrane depolarization and inhibits oxygen consumptionpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage796por
oaire.citation.issue101por
oaire.citation.startPage789por
oaire.citation.titleJournal of Inorganic Biochemistrypor
person.familyNameSoares
person.familyNameGutierrez-Merino
person.familyNameAureliano
person.givenNameSandra
person.givenNameCarlos
person.givenNameManuel
person.identifier584146
person.identifier.ciencia-idAA14-3490-DC5E
person.identifier.orcid0000-0002-6562-2674
person.identifier.orcid0000-0003-3673-7007
person.identifier.orcid0000-0003-4858-3201
person.identifier.ridK-4574-2014
person.identifier.ridI-3283-2012
person.identifier.scopus-author-id10539327200
person.identifier.scopus-author-id6603412860
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicationa98c149e-2a56-41b3-95fa-a45ae08599e6
relation.isAuthorOfPublication1edd3bda-28a9-4d7f-a404-f867f72ddefa
relation.isAuthorOfPublicationbb413661-7edd-4b57-8338-33889cfd05db
relation.isAuthorOfPublication.latestForDiscoverybb413661-7edd-4b57-8338-33889cfd05db

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