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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/122879
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dc.contributor.authorSilva, Danilo Grünig Humberto da-
dc.contributor.authorRicci Júnior, Octávio-
dc.contributor.authorAlmeida, Eduardo Alves de-
dc.contributor.authorBonini-Domingos, Claudia Regina-
dc.date.accessioned2015-04-27T11:56:07Z-
dc.date.accessioned2016-10-25T20:47:14Z-
dc.date.available2015-04-27T11:56:07Z-
dc.date.available2016-10-25T20:47:14Z-
dc.date.issued2014-
dc.identifierhttp://onlinelibrary.wiley.com/doi/10.1111/jpi.12204/abstract-
dc.identifier.citationJournal of Pineal Research, v. 58, n. 2, p. 178-188, 2014.-
dc.identifier.issn0742-3098-
dc.identifier.urihttp://hdl.handle.net/11449/122879-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/122879-
dc.description.abstractThis study aimed to assess antioxidant effects of melatonintreatment compared to N-acetylcysteine (NAC) and to their combination in asickle cell suspension. Sickle erythrocytes were suspended in phosphate-buffered saline, pH 7.4, composing external control group. They were alsosuspended and incubated at 37°C either in the absence (experimental controlgroup) or in the presence of NAC, melatonin and their combination atconcentrations of 100 pM, 100 nM and 100 lM for 1 hr (treatment groups).The melatonin influences were evaluated by spectrophotometric [hemolysisdegree, catalase (CAT), glutathione S-transferase (GST), glutathioneperoxidase (GPx), glutathione reductase (GR), glucose-6-phosphatedehydrogenase (G6PDH), and superoxide dismutase (SOD) activities] andchromatographic methods [glutathione (GSH) and malondialdehyde (MDA)levels]. Incubation period was able to cause a rise about 64% on hemolysisdegree as well as practically doubled the lipid peroxidation levels (P < 0.01).However, almost all antioxidants tested treatments neutralized this incubationeffect observed in MDA levels. Among the antioxidant biomarkers evaluated,we observed a modulating effect of combined treatment on GPx and SODactivities (P < 0.01), which showed ~25% decrease in their activities. Inaddition, we found an antioxidant dose-dependent effect for melatonin onlipid peroxidation (r = 0.29; P = 0.03) and for combined antioxidanttreatments also on MDA levels (r = 0.37; P = 0.01) and on SOD activity(r = 0.54; P < 0.01). Hence, these findings contribute with important insightthat melatonin individually or in combination with NAC may be useful forsickle cell anemia management.en
dc.format.extent178-188-
dc.language.isoeng-
dc.sourceCurrículo Lattes-
dc.subjectalternative therapyen
dc.subjectantioxidant capacityen
dc.subjecthemoglobin Sen
dc.subjectmelatoninen
dc.subjectoxidative stressen
dc.titlePotential utility of melatonin as an antioxidant therapy in the management of sickle cell anemiaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto (FAMERP)-
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Biologia, Instituto de Biociências Letras e Ciências Exatas de São José do Rio Preto, Sao Jose do Rio Preto, Rua Cristóvão Colombo, 2265, Jardim Nazareth, CEP 15054-000, SP, Brasil-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Biologia, Instituto de Biociências Letras e Ciências Exatas de São José do Rio Preto-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Química e Ciências Ambientais, Instituto de Biociências Letras e Ciências Exatas de São José do Rio Preto-
dc.identifier.doihttp://dx.doi.org/10.1111/jpi.12204-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Pineal Research-
dc.identifier.lattes3279428066176719-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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