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dc.contributor.authorYildizbayrak, Nebahat
dc.contributor.authorErkan, Melike
dc.contributor.authorORTA YILMAZ, Banu
dc.date.accessioned2023-05-29T11:41:00Z
dc.date.available2023-05-29T11:41:00Z
dc.date.issued2020
dc.identifier.citationORTA YILMAZ B., Yildizbayrak N., Erkan M., "Sodium arsenite-induced detriment of cell function in Leydig and Sertoli cells: the potential relation of oxidative damage and antioxidant defense system", Drug and Chemical Toxicology, cilt.43, sa.5, ss.479-487, 2020
dc.identifier.issn0148-0545
dc.identifier.otherav_0a66b91d-2445-45ad-83c3-e10ff6caac69
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/188679
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053373326&origin=inward
dc.identifier.urihttps://doi.org/10.1080/01480545.2018.1505902
dc.description.abstractArsenic is commonly found in the natural environment and is toxic agent for living organism in many countries in the world. Studies on animal models suggest that exposure to arsenic may cause reproductive toxicity; however, effect of arsenic on reproductive toxicity has still not been clearly described. This study was focused on cytotoxicity, oxidative stress, and the antioxidant defense system induced with exposure to sodium arsenite in Mus musculus Leydig and Sertoli cells. The cells were exposed to two different concentrations of sodium arsenite of 50 ppb (0.4 μM) and 1000 ppb (7.7 μM) for 24, 48, and 72 h. Following the exposure time, cell viability, cell proliferation, and lactate dehydrogenase (LDH) activity were determining using colorimetric method. Also, we evaluated oxidative stress markers such as glutathione (GSH), lipid peroxidation, hydroxyl radical, hydrogen peroxide levels, and cellular enzymatic antioxidants such as catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-s-transferase, and γ-glutamyl transpeptidase (γ-GT). As a result, sodium arsenite exposure in Leydig and Sertoli cells caused cellular cytotoxicity and downregulated the antioxidant defense system by inducing oxidative stress depending on concentration and time. Furthermore, this study demonstrated that when compared with Sertoli cells, Leydig cells were more affected by arsenite toxicity.
dc.language.isoeng
dc.subjectKimya Mühendisliği ve Teknolojisi
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectMühendislik ve Teknoloji
dc.subjectToksikoloji
dc.subjectFarmakoloji
dc.subjectHalk, Çevre ve İş Sağlığı
dc.subjectSağlık, Toksikoloji ve Mutajenez
dc.subjectFizik Bilimleri
dc.subjectKimyasal Sağlık ve Güvenlik
dc.subjectSağlık Bilimleri
dc.subjectMühendislik, Bilişim ve Teknoloji (ENG)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSosyal Bilimler (SOC)
dc.subjectMühendislik
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectSosyal Bilimler Genel
dc.subjectMÜHENDİSLİK, KİMYASAL
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectTOKSİKOLOJİ
dc.subjectKAMU, ÇEVRE VE İŞ SAĞLIĞI
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectSosyal ve Beşeri Bilimler
dc.subjectSosyoloji
dc.titleSodium arsenite-induced detriment of cell function in Leydig and Sertoli cells: the potential relation of oxidative damage and antioxidant defense system
dc.typeMakale
dc.relation.journalDrug and Chemical Toxicology
dc.contributor.departmentİstanbul Üniversitesi , Fen Fakültesi , Biyoloji Bölümü
dc.identifier.volume43
dc.identifier.issue5
dc.identifier.startpage479
dc.identifier.endpage487
dc.contributor.firstauthorID4266866


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