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dc.contributor.authorAkça, Görkem
dc.contributor.authorEren, Hüseyin
dc.contributor.authorTümkaya, Levent
dc.contributor.authorMercantepe, Tolga
dc.contributor.authorHorsanali, Mustafa Ozan
dc.contributor.authorDeveci, Ezgi
dc.contributor.authorYılmaz, Adnan
dc.date.accessioned2020-12-19T19:41:56Z
dc.date.available2020-12-19T19:41:56Z
dc.date.issued2018
dc.identifier.citationAkca, G., Eren, H., Tumkaya, L., Mercantepe, T., Horsanali, M. O., Deveci, E., Dil, E., & Yilmaz, A. (2018). The protective effect of astaxanthin against cisplatin-induced nephrotoxicity in rats. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 100, 575–582. https://doi.org/10.1016/j.biopha.2018.02.042en_US
dc.identifier.issn0753-3322
dc.identifier.issn1950-6007
dc.identifier.urihttps://doi.org/10.1016/j.biopha.2018.02.042
dc.identifier.urihttps://hdl.handle.net/11436/1856
dc.descriptionHORSANALI, Mustafa Ozan/0000-0002-3651-0948; Mercantepe, Tolga/0000-0002-8506-1755; yilmaz, adnan/0000-0003-4842-1173en_US
dc.descriptionWOS: 000427649200067en_US
dc.descriptionPubMed: 29494988en_US
dc.description.abstractPurpose: the aim of this experimental study was to investigate the antioxidant effects of astaxanthin against cisplatin-induced nephrotoxicity in rats. Methods: Forty-eight male Sprague-Dawley rats weighing 264.83 +/- 7.39 g were randomly divided into six groups of eight animals each. These were constituted as control, olive oil control, astaxanthin control, cisplatin control, 16 mg/kg cisplatin & 25 mg/kg astaxanthin and 16 mg/kg cisplatin & 75 mg/kg astaxanthin groups. Biochemical evaluation was performed by measuring blood urea nitrogen, serum creatinine, total oxidant status and total antioxidant status. Renal corpuscle, proximal and distal tubules areas (mu m(2)) were calculated for histopathological evaluation, and Caspase-3 staining was performed for immunohistochemical evaluation. Results: Cisplatin reduced total antioxidant status levels and increased blood urea nitrogen, serum creatinine, total oxidant status, and Caspase-3 levels. It also caused dilatation, vacuolization, and loss of tubular epithelial cells in the proximal and distal tubules, and glomerular degeneration and edema were determined in kidney tissue (p < 0.05). Administration of 25 mg and 75 mg astaxanthin increased total antioxidant status levels, reduced blood urea nitrogen, serum creatinine, total oxidant status, and Caspase-3, and ameliorated degenerative distal and proximal tubules, glomerular degeneration and edema in kidney tissue (p < 0.05). Conclusions: the nephrotoxic effect of cisplatin was diminished by the antioxidant effect of astaxanthin.en_US
dc.language.isoengen_US
dc.publisherElsevier France-Editions Scientifiques Medicales Elsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAstaxanthinen_US
dc.subjectAntioxidanten_US
dc.subjectCisplatinen_US
dc.subjectNephrotoxicityen_US
dc.subjectOxidanten_US
dc.titleThe protective effect of astaxanthin against cisplatin-induced nephrotoxicity in ratsen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorAkça, Görkem
dc.contributor.institutionauthorEren, Hüseyin
dc.contributor.institutionauthorTümkaya, Levent
dc.contributor.institutionauthorMercantepe, Tolga
dc.contributor.institutionauthorHorsanali, Mustafa Ozan
dc.contributor.institutionauthorHorsanali, Mustafa Ozan
dc.contributor.institutionauthorDeveci, Ezgi
dc.contributor.institutionauthorYılmaz, Adnan
dc.identifier.doi10.1016/j.biopha.2018.02.042
dc.identifier.volume100en_US
dc.identifier.startpage575en_US
dc.identifier.endpage582en_US
dc.relation.journalBiomedicine & Pharmacotherapyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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