Toxicity of copper intake: lipid profile, oxidative stress and susceptibility to renal dysfunction

dc.contributor.authorGalhardi, C. M.
dc.contributor.authorDiniz, Y. S.
dc.contributor.authorFaine, L. A.
dc.contributor.authorRodrigues, H. G.
dc.contributor.authorBurneiko, RCM
dc.contributor.authorRibas, B. O.
dc.contributor.authorNovelli, ELB
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionMinist Sanidad & Consumo
dc.date.accessioned2014-05-20T13:53:21Z
dc.date.available2014-05-20T13:53:21Z
dc.date.issued2004-12-01
dc.description.abstractThe present study was carried out to investigate the effects of copper (Cu) intake on lipid profile, oxidative stress and tissue damage in normal and in diabetic condition. Since diabetes mellitus is a situation of high-risk susceptibility to toxic compounds, we examined potential early markers of Cu excess in diabetic animals. Male Wistar rats, at 60-days-old were divided into six groups of eight rats each. The control(C) received saline from gastric tube, the no-diabetic(Cu-10), treated with 10 mg/kg of Cu(Cu(++)-CuSO(4), gastric tube), no-diabetic with Cu-60mg/kg(Cu-60), diabetic(D), diabetic low-Cu(DCu-10) and diabetic high-Cu(DCu-60). Diabetes was induced by an ip injection of streptozotocin (60mg/kg). After 30 days of treatments, no changes we're observed in serum lactate dehydrogenase, alanine transaminase and alkaline phosphatase; indicating no adverse effects on cardiac and hepatic tissues. D-rats had glucose intolerance and dyslipidemic profile. Cholesterol and LDL-cholesterol were higher in Cu-60 and DCu-60 than in C, Cu-10 and D and DCu-10 groups respectively. Cu-60 rats had higher lipid hydroperoxide (HP) and lower superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) serum activities than C and Cu-10 rats. LH was increased and GSH-Px was decreased, while no alterations were observed in SOD and catalase in serum of DCu-60 animals. DCu-60 rats had increased urinary glucose, creatinine and albumin. In conclusion, Cu intake at high concentration induced adverse effects on lipid profile, associated with oxidative stress and diminished activities of antioxidant enzymes. Diabetic animals were more susceptible to copper toxicity. High Cu intake induced dyslipidemic profile, oxidative stress and kidney dysfunction in diabetic condition. Copper renal toxicity was associated with oxidative stress and reduction at least, one of the antioxidant enzymes. (C) 2004 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniv Estadual Paulista, Inst Biol Sci, Dept Chem & Biochem, Botucatu, SP, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Med, Dept Clin & Cardiol, Postgrad Course, Botucatu, SP, Brazil
dc.description.affiliationMinist Sanidad & Consumo, Inst Salud Carlos III, Dept Toxicol, Madrid, Spain
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biol Sci, Dept Chem & Biochem, Botucatu, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Med, Dept Clin & Cardiol, Postgrad Course, Botucatu, SP, Brazil
dc.format.extent2053-2060
dc.identifierhttp://dx.doi.org/10.1016/j.fct.2004.07.020
dc.identifier.citationFood and Chemical Toxicology. Oxford: Pergamon-Elsevier B.V., v. 42, n. 12, p. 2053-2060, 2004.
dc.identifier.doi10.1016/j.fct.2004.07.020
dc.identifier.issn0278-6915
dc.identifier.urihttp://hdl.handle.net/11449/19042
dc.identifier.wosWOS:000225252500016
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofFood and Chemical Toxicology
dc.relation.ispartofjcr3.977
dc.relation.ispartofsjr1,144
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectcopperpt
dc.subjectlipid profilept
dc.subjectoxidative stresspt
dc.subjectkidneypt
dc.subjectDiabetes mellituspt
dc.titleToxicity of copper intake: lipid profile, oxidative stress and susceptibility to renal dysfunctionen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.orcid0000-0002-6122-0379[4]
unesp.author.orcid0000-0001-8741-1336[1]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentQuímica e Bioquímica - IBBpt

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