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dc.contributor.authorIlgın, Sinem
dc.contributor.authorAydoğan-Kılıc, G.
dc.contributor.authorBaysal, Merve
dc.contributor.authorKılıç, Volkan
dc.contributor.authorKorkut, Büşra
dc.contributor.authorUçarcan, Şeyda
dc.contributor.authorAtlı Eklioğlu, Özlem
dc.date.accessioned2019-10-19T16:02:50Z
dc.date.available2019-10-19T16:02:50Z
dc.date.issued2017
dc.identifier.issn2472-1727
dc.identifier.urihttps://dx.doi.org/10.1002/bdr2.1010
dc.identifier.urihttps://hdl.handle.net/11421/13943
dc.descriptionWOS: 000399733100002en_US
dc.descriptionPubMed ID: 28398617en_US
dc.description.abstractBackground: Citalopram hydrobromide (CTL) has been shown to cause sexual dysfunction; however, its reproductive toxicity potential has not been sufficiently elucidated in men. Therefore, we aimed to clarify the toxic effects of CTL on the reproductive system of male rats. Methods: For this purpose, CTL was administered at 5, 10, and 20 mg/kg/day to rats orally for 28 days. Sperm concentration, motility, and morphology were investigated using a computer-assisted sperm analysis system, and sperm DNA damage was detected using a Comet assay. The testes were histopathologically examined. Serum follicle-stimulating hormone, luteinizing hormone, and testosterone levels were measured and the oxidative status of testes was investigated. Results: Our results showed that sperm concentration was reduced, and abnormal sperm morphology and sperm DNA damage were increased in CTL-administered groups. Additionally, histopathological changes were observed in the testes of CTL-administered rats. Luteinizing hormone levels were increased in CTL-administered groups, while testosterone levels were increased in the 5 and 10 mg/kg CTL-administered groups. Decreased glutathione signaled enhanced oxidative stress in the 10 and 20 mg/kg CTL-administered groups. Conclusion: Thus, we concluded that CT induced testicular damage in male rats; this testicular damage was accompanied by oxidative stress and hormonal changes, which are considered as the important causes of reproductive disordersen_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/bdr2.1010en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCitalopramen_US
dc.subjectReproductive Toxicityen_US
dc.subjectOxidative Stressen_US
dc.subjectDna Damageen_US
dc.titleCitalopram Induces Reproductive Toxicity in Male Ratsen_US
dc.typearticleen_US
dc.relation.journalBirth Defects Researchen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Toksikoloji Anabilim Dalıen_US
dc.identifier.volume109en_US
dc.identifier.issue7en_US
dc.identifier.startpage475en_US
dc.identifier.endpage485en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorIlgın, Sinem
dc.contributor.institutionauthorAydoğan-Kılıc, G.
dc.contributor.institutionauthorKılıç, Volkan
dc.contributor.institutionauthorUçarcan, Şeyda
dc.contributor.institutionauthorAtlı Eklioğlu, Özlem


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