dc.contributor | Universidade Estadual Paulista (UNESP) | |
dc.creator | Silva, Danilo Grünig Humberto da | |
dc.creator | Ricci Júnior, Octávio | |
dc.creator | Almeida, Eduardo Alves de | |
dc.creator | Bonini-Domingos, Claudia Regina | |
dc.date | 2015-04-27T11:56:07Z | |
dc.date | 2016-10-25T20:47:14Z | |
dc.date | 2015-04-27T11:56:07Z | |
dc.date | 2016-10-25T20:47:14Z | |
dc.date | 2014 | |
dc.date.accessioned | 2017-04-06T08:11:00Z | |
dc.date.available | 2017-04-06T08:11:00Z | |
dc.identifier | Journal of Pineal Research, v. 58, n. 2, p. 178-188, 2014. | |
dc.identifier | 0742-3098 | |
dc.identifier | http://hdl.handle.net/11449/122879 | |
dc.identifier | http://acervodigital.unesp.br/handle/11449/122879 | |
dc.identifier | http://dx.doi.org/10.1111/jpi.12204 | |
dc.identifier | 3279428066176719 | |
dc.identifier | http://onlinelibrary.wiley.com/doi/10.1111/jpi.12204/abstract | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/933496 | |
dc.description | This 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.language | eng | |
dc.relation | Journal of Pineal Research | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | alternative therapy | |
dc.subject | antioxidant capacity | |
dc.subject | hemoglobin S | |
dc.subject | melatonin | |
dc.subject | oxidative stress | |
dc.title | Potential utility of melatonin as an antioxidant therapy in the management of sickle cell anemia | |
dc.type | Otro | |