dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorSilva, Danilo Grünig Humberto da
dc.creatorRicci Júnior, Octávio
dc.creatorAlmeida, Eduardo Alves de
dc.creatorBonini-Domingos, Claudia Regina
dc.date2015-04-27T11:56:07Z
dc.date2016-10-25T20:47:14Z
dc.date2015-04-27T11:56:07Z
dc.date2016-10-25T20:47:14Z
dc.date2014
dc.date.accessioned2017-04-06T08:11:00Z
dc.date.available2017-04-06T08:11:00Z
dc.identifierJournal of Pineal Research, v. 58, n. 2, p. 178-188, 2014.
dc.identifier0742-3098
dc.identifierhttp://hdl.handle.net/11449/122879
dc.identifierhttp://acervodigital.unesp.br/handle/11449/122879
dc.identifierhttp://dx.doi.org/10.1111/jpi.12204
dc.identifier3279428066176719
dc.identifierhttp://onlinelibrary.wiley.com/doi/10.1111/jpi.12204/abstract
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/933496
dc.descriptionThis 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.
dc.languageeng
dc.relationJournal of Pineal Research
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectalternative therapy
dc.subjectantioxidant capacity
dc.subjecthemoglobin S
dc.subjectmelatonin
dc.subjectoxidative stress
dc.titlePotential utility of melatonin as an antioxidant therapy in the management of sickle cell anemia
dc.typeOtro


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