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dc.contributor.authorFındık, Hüseyin
dc.contributor.authorTümkaya, Levent
dc.contributor.authorYılmaz, Adnan
dc.contributor.authorAslan, Mehmet Gökhan
dc.contributor.authorOkutucu, Murat
dc.contributor.authorAkyıldız, Kerimali
dc.contributor.authorMercantepe, Tolga
dc.date.accessioned2020-12-19T19:40:39Z
dc.date.available2020-12-19T19:40:39Z
dc.date.issued2019
dc.identifier.citationFındık, H., Tumkaya, L., Yılmaz, A., Gökhan Aslan, M., Okutucu, M., Akyildiz, K., & Mercantepe, T. (2019). The protective effects of astaxanthin against cisplatin-induced retinal toxicity. Cutaneous and ocular toxicology, 38(1), 59–65. https://doi.org/10.1080/15569527.2018.1518330en_US
dc.identifier.issn1556-9527
dc.identifier.issn1556-9535
dc.identifier.urihttps://doi.org/10.1080/15569527.2018.1518330
dc.identifier.urihttps://hdl.handle.net/11436/1611
dc.descriptionMercantepe, Tolga/0000-0002-8506-1755; Aslan, Mehmet Gokhan/0000-0002-3250-1606; Findik, Huseyin/0000-0001-7343-8757; yilmaz, adnan/0000-0003-4842-1173en_US
dc.descriptionWOS: 000457026400010en_US
dc.descriptionPubMed: 30185066en_US
dc.description.abstractPurpose: This study investigated the toxic effects of an antineoplastic agent, cisplatin (CIS), on retinal cells and the potential capacity of astaxanthin (ASTA) to elicit a future therapeutic protocol in CIS-induced retinal toxicity. Materials and methods: Six groups were formed for the assessment; control (healthy; Group 1), olive oil (olive oil only; Group 2), ASTA control group (ASTA only, Group 3), the single intraperitoneal (IP) dose of 16 mg/kg CIS (CIS only group; Group 4), 16 mg/kg CIS +25 mg/kg (IP) ASTA (Group 5), and 16 mg/kg CIS +75 mg/kg (IP) ASTA (Group 6). on the third day after CIS administration, rats in all groups were sacrificed under anesthesia and the analysis of the biochemical parameters and histopathological levels were performed. Results: A significant decrease in GSH levels and increases in MDA, eNOS, and 8-OHdG expressions were recorded. Additionally, CIS treatment had caused acidophilic staining in retinal histological appearance. ASTA treatment reduced the increases in MDA, eNOS, and 8-OHdG levels following CIS administration and increased the levels of GSH expressions, as well. Conclusions: These results may suggest that the ASTA molecule as a promising option to prevent retinal toxicity in patients receiving CIS treatment for malignant tumors.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAstaxanthinen_US
dc.subjectChemotherapyen_US
dc.subjectCisplatin toxicityen_US
dc.subjecteNOSen_US
dc.subjectOxidative stressen_US
dc.subjectRetinaen_US
dc.titleThe protective effects of astaxanthin against cisplatin-induced retinal toxicityen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorFındık, Hüseyin
dc.contributor.institutionauthorTümkaya, Levent
dc.contributor.institutionauthorYılmaz, Adnan
dc.contributor.institutionauthorAslan, Mehmet Gökhan
dc.contributor.institutionauthorOkutucu, Murat
dc.contributor.institutionauthorAkyıldız, Kerimali
dc.contributor.institutionauthorMercantepe, Tolga
dc.identifier.doi10.1080/15569527.2018.1518330
dc.identifier.volume38en_US
dc.identifier.issue1en_US
dc.identifier.startpage59en_US
dc.identifier.endpage65en_US
dc.relation.journalCutaneous and Ocular Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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