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dc.contributor.authorSener, Tarik Emre
dc.contributor.authorSener, Goksel
dc.contributor.authorCevik, Ozge
dc.contributor.authorEker, Pinar
dc.contributor.authorCetinel, Sule
dc.contributor.authorTraxer, Olivier
dc.contributor.authorTanidir, Yiloren
dc.contributor.authorAkbal, Cem
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:44:22Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:44:22Z
dc.date.issued2017
dc.identifier.issn0090-4295
dc.identifier.issn1527-9995
dc.identifier.urihttps://dx.doi.org/10.1016/j.urology.2016.09.032
dc.identifier.urihttps://hdl.handle.net/20.500.12418/7036
dc.descriptionWOS: 000396525000087en_US
dc.descriptionPubMed ID: 27717860en_US
dc.description.abstractOBJECTIVE To evaluate the protective effects of melatonin (Mel) on an ethylene glycol (EG)-induced nephrolithiasis model in rats. MATERIALS AND METHODS Thirty-two Wistar albino rats were divided into 4 groups: control, EG, prevention Mel (Mel + EG + Mel), and therapeutic Mel (EG + Mel). EG (0.75%) was added to drinking water to create nephrolithiasis model. The EG group received EG and the Mel + EG + Mel group received both EG and Mel for 8 weeks. In the EG + Mel group, EG is given for 8 weeks and Mel is given for the last 4 weeks of the experiment. At the end of experimental period, urine, blood samples, and tissues were collected. RESULTS In 24-hour urine samples, calcium, citrate, and creatinine levels were decreased and oxalate levels were increased in the EG group, whereas Mel prevention and Mel treatment reversed these parameters back to control levels. Malondialdehyde, glutathione activities, myeloperoxidase, superoxide dismutase levels, and caspase-3 activity showed improvements in the Mel-treated groups when compared with the EG group. 8-Hydroxydeoxyguanosine, matrix metalloproteinase 9 levels, N-acetyl-beta-glucosaminidase activity, and osteopontin mRNA expression were elevated in the EG group and decreased back to control levels in the Mel + EG + Mel and EG + Mel groups. Histological examination showed improvement in the Mel-treated groups when compared with the EG group. CONCLUSION Mel can prevent crystalluria and kidney damage due to crystal formation and aggregation. It can be considered as a potential prophylactic and protective agent in high-risk patients with urinary stone formation or recurrence if supported by further clinical studies. (C) 2016 Elsevier Inc.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE INCen_US
dc.relation.isversionof10.1016/j.urology.2016.09.032en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe Effects of Melatonin on Ethylene Glycol-induced Nephrolithiasis: Role on Osteopontin mRNA Gene Expressionen_US
dc.typearticleen_US
dc.relation.journalUROLOGYen_US
dc.contributor.departmentMarmara Univ, Sch Med, Dept Urol, Istanbul, Turkey -- Marmara Univ, Sch Pharm, Dept Pharmacol, Istanbul, Turkey -- Cumhuriyet Univ, Sch Pharm, Dept Biochem, Sivas, Turkey -- Umraniye Training & Res Hosp, Dept Biochem, Istanbul, Turkey -- Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkey -- Pierre & Marie Curie Univ, Tenon Univ Hosp, Dept Urol, Paris, Franceen_US
dc.contributor.authorIDAkbal, Cem -- 0000-0003-2202-6909; Cevik, Ozge -- 0000-0002-9325-3757en_US
dc.identifier.volume99en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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