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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130470
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dc.contributor.authorPereira, R. S.-
dc.date.accessioned2014-05-27T11:18:06Z-
dc.date.accessioned2016-10-25T21:21:14Z-
dc.date.available2014-05-27T11:18:06Z-
dc.date.available2016-10-25T21:21:14Z-
dc.date.issued1996-08-07-
dc.identifierhttp://dx.doi.org/10.1007/BF03190274-
dc.identifier.citationEuropean Journal of Drug Metabolism and Pharmacokinetics, v. 21, n. 1, p. 23-26, 1996.-
dc.identifier.issn0378-7966-
dc.identifier.urihttp://hdl.handle.net/11449/130470-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130470-
dc.description.abstractWhen calcinine (A-23187) (2 mu M), a known Ca2+ ionophore, is present, a significant protection is observed to a mitochondrial suspension undergoing lipid peroxidation by Fe2+-citrate complex. A-23187 can remove Ca2+, which seems to have an important role in the lipid peroxidation process, from its 'lesive sites' and consequently preventing the damage. This information has importance in terms of knowing the mechanisms and avoiding the damages of lipid peroxidation that occur in some pathological cases such as tumor promotion and hemochromatosis.en
dc.format.extent23-26-
dc.language.isoeng-
dc.publisherMedecine Et Hygiene-
dc.sourceScopus-
dc.subjectA-23187-
dc.subjectCa2+-
dc.subjectLipid peroxidation-
dc.subjectMitochondria-
dc.subjectCalcimycin-
dc.subjectCalcium ion-
dc.subjectFerric citrate-
dc.subjectAnimal tissue-
dc.subjectControlled study-
dc.subjectHemochromatosis-
dc.subjectLipid peroxidation-
dc.subjectMitochondrion-
dc.subjectNonhuman-
dc.subjectRat-
dc.subjectTumor promotion-
dc.subjectAnimals-
dc.subjectCalcimycin-
dc.subjectCalcium-
dc.subjectIonophores-
dc.subjectLipid Peroxidation-
dc.subjectMembrane Potentials-
dc.subjectMitochondria, Liver-
dc.subjectRats-
dc.subjectRats, Wistar-
dc.subjectReactive Oxygen Species-
dc.titleLipid peroxidation: the role or Ca2+ and protection by calcinineen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Biochemistry Institute of Chemistry Universidade Estadual Paulista (UNESP), Araraquara, São Paulo-
dc.description.affiliationDepartment of Biochemistry Institute of Chemistry Universidade Estadual Paulista (UNESP), C.P. 355, Araraquara, S.P. 14801-970-
dc.description.affiliationUnespDepartment of Biochemistry Institute of Chemistry Universidade Estadual Paulista (UNESP), Araraquara, São Paulo-
dc.description.affiliationUnespDepartment of Biochemistry Institute of Chemistry Universidade Estadual Paulista (UNESP), C.P. 355, Araraquara, S.P. 14801-970-
dc.identifier.doi10.1007/BF03190274-
dc.identifier.wosWOS:A1996UY20800005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofEuropean Journal of Drug Metabolism and Pharmacokinetics-
dc.identifier.scopus2-s2.0-0030035915-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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