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http://acervodigital.unesp.br/handle/11449/69095
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DC Field | Value | Language |
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dc.contributor.author | Behling, Estela B. | - |
dc.contributor.author | Sendão, Milena C. | - |
dc.contributor.author | Francescato, Heloísa D.C. | - |
dc.contributor.author | Antunes, Lusânia M.G. | - |
dc.contributor.author | Costa, Roberto S. | - |
dc.contributor.author | Bianchi, Maria de Lourdes P. | - |
dc.date.accessioned | 2014-05-27T11:21:58Z | - |
dc.date.accessioned | 2016-10-25T18:22:41Z | - |
dc.date.available | 2014-05-27T11:21:58Z | - |
dc.date.available | 2016-10-25T18:22:41Z | - |
dc.date.issued | 2006-09-20 | - |
dc.identifier | http://www.if-pan.krakow.pl/pjp/cont06.html#No4 | - |
dc.identifier | http://www.if-pan.krakow.pl/pjp/pdf/2006/4_526.pdf | - |
dc.identifier.citation | Pharmacological Reports, v. 58, n. 4, p. 526-532, 2006. | - |
dc.identifier.issn | 1734-1140 | - |
dc.identifier.uri | http://hdl.handle.net/11449/69095 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/69095 | - |
dc.description.abstract | Quercetin, a typical bioflavonoid ubiquitously present in fruits and vegetables, is considered to be helpful for human health. Cisplatin (cDDP) is one of the most active cytotoxic agents in the treatment of a wide range of solid tumors. The aim of this study was to investigate the possible effect of quercetin, a bioflavonoid with antioxidant potential, on cisplatin-induced nophrotoxicity and lipid peroxidation in rats. Gavage administrations of water, propylene glycol and quercetin (50 mg/kg) were made 24 and 1 h before saline or cDDP (5 mg/kg) ip injections and were repeated daily for 2, 5 or 20 subsequent days. Rats were killed 2, 5 and 20 days after ip injections, and blood and urine samples were collected to determine plasma creatinine, urine volume and osmolality. The kidneys were removed to determine the levels of thiobarbituric acid-reactive substances (TBARS) and for histological studies. Cisplatin increased lipid peroxidation, urine volume and plasma creatinine levels and decreased urine osmolality. Treatment with quercetin attenuated these alterations. These results demonstrate the role of oxidative stress and suggest a protective effect of quercetin on cisplatin-induced nephrotoxicity in adult Wistar rats. Copyright © 2006 by Institute of Pharmacology Polish Academy of Sciences. | en |
dc.format.extent | 526-532 | - |
dc.language.iso | eng | - |
dc.source | Scopus | - |
dc.subject | Antioxidants | - |
dc.subject | Cisplatin | - |
dc.subject | Lipid peroxidation | - |
dc.subject | Nephrotoxicity | - |
dc.subject | Quercetin | - |
dc.subject | antioxidant | - |
dc.subject | cisplatin | - |
dc.subject | creatinine | - |
dc.subject | flavanoid | - |
dc.subject | platinil | - |
dc.subject | propylene glycol | - |
dc.subject | quercetin | - |
dc.subject | sodium chloride | - |
dc.subject | thiobarbituric acid reactive substance | - |
dc.subject | water | - |
dc.subject | animal experiment | - |
dc.subject | animal model | - |
dc.subject | animal tissue | - |
dc.subject | comparative study | - |
dc.subject | controlled study | - |
dc.subject | creatinine blood level | - |
dc.subject | drug effect | - |
dc.subject | histopathology | - |
dc.subject | lipid peroxidation | - |
dc.subject | male | - |
dc.subject | multiple drug dose | - |
dc.subject | nephrotoxicity | - |
dc.subject | nonhuman | - |
dc.subject | oxidative stress | - |
dc.subject | rat | - |
dc.subject | rat strain | - |
dc.subject | urine osmolality | - |
dc.subject | urine volume | - |
dc.subject | Animals | - |
dc.subject | Antineoplastic Agents | - |
dc.subject | Creatinine | - |
dc.subject | Free Radical Scavengers | - |
dc.subject | Kidney | - |
dc.subject | Kidney Diseases | - |
dc.subject | Kidney Function Tests | - |
dc.subject | Lipid Peroxidation | - |
dc.subject | Male | - |
dc.subject | Oxidative Stress | - |
dc.subject | Rats | - |
dc.subject | Rats, Wistar | - |
dc.subject | Time Factors | - |
dc.title | Comparative study of multiple dosage of quercetin against cisplatin-induced nephrotoxicity and oxidative stress in rat kidneys | en |
dc.type | outro | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.description.affiliation | Departamento de Alimentos e Nutrição Faculdade de Ciencias Farmaceuticas de Araraquara UNESP, Rod. Araraquara/Jaú, km 01, 14801-902 Araraquara SP | - |
dc.description.affiliation | Departamento de Análises Clínicas Toxicológicas e Bromatológicas Faculdade de Ciencias Farmaceuticas de Ribeirão Universidade de São Paulo, Av. do Café, s/n, 14040-903 Ribeirão Preto, SP | - |
dc.description.affiliation | Departamento de Patologia Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, Av. Bandeirantes, 3900, 14040-903 Ribeirão Preto, SP | - |
dc.description.affiliationUnesp | Departamento de Alimentos e Nutrição Faculdade de Ciencias Farmaceuticas de Araraquara UNESP, Rod. Araraquara/Jaú, km 01, 14801-902 Araraquara SP | - |
dc.identifier.wos | WOS:000241940100008 | - |
dc.rights.accessRights | Acesso aberto | - |
dc.identifier.file | 2-s2.0-33748663525.pdf | - |
dc.relation.ispartof | Pharmacological Reports | - |
dc.identifier.scopus | 2-s2.0-33748663525 | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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