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dc.contributor.authorOzcagli, Eren
dc.contributor.authorAlpertunga, Büket
dc.contributor.authorFENGA, Concettina
dc.contributor.authorBerktas, Mehmet
dc.contributor.authorTSITSIMPIKOU, Christina
dc.contributor.authorWilks, Martin F.
dc.contributor.authorTsatsakis, Aristidis M.
dc.date.accessioned2021-03-04T07:51:37Z
dc.date.available2021-03-04T07:51:37Z
dc.identifier.citationOzcagli E., Alpertunga B., FENGA C., Berktas M., TSITSIMPIKOU C., Wilks M. F. , Tsatsakis A. M. , "Effects of 3-monochloropropane-1,2-diol (3-MCPD) and its metabolites on DNA damage and repair under in vitro conditions", FOOD AND CHEMICAL TOXICOLOGY, cilt.89, ss.1-7, 2016
dc.identifier.issn0278-6915
dc.identifier.otherav_60466e1d-dc72-4b20-950e-8217c181c20f
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/67202
dc.identifier.urihttps://doi.org/10.1016/j.fct.2015.12.027
dc.description.abstract3-monochloropropane-1,2-diol (3-MCPD) is a food contaminant that occurs during industrial production processes and can be found mainly in fat and salt containing products. 3-MCPD has exhibited mutagenic activity in vitro but not in vivo, however, a genotoxic mechanism for the occurrence of kidney tumors has not so far been excluded. The main pathway of mammalian 3-MCPD metabolism is via the formation of - chlorolactatic acid and formation of glycidol has been demonstrated in bacterial metabolism. The aim of this study was to investigate genotoxic and oxidative DNA damaging effects of 3-MCPD and its metabolites, and to provide a better understanding of their roles in DNA repair processes. DNA damage was assessed by alkaline comet assay in target rat kidney epithelial cell lines (NRK-52E) and human embryonic kidney cells (HEK-293). Purine and pyrimidine base damage, H2O2 sensitivity and DNA repair capacity were assessed via modified comet assay. The results revealed in vitro evidence for increased genotoxicity and H2O2 sensitivity. No association was found between oxidative DNA damage and DNA repair capacity with the exception of glycidol treatment at 20 mu g/mL. These findings provide further insights into the mechanisms underlying the in vitro genotoxic potential of 3-MCPD and metabolites. (C) 2016 Elsevier Ltd. All rights reserved.
dc.language.isoeng
dc.subjectFarmasötik Toksikoloji
dc.subjectGIDA BİLİMİ VE TEKNOLOJİSİ
dc.subjectTarım Bilimleri
dc.subjectTarım ve Çevre Bilimleri (AGE)
dc.subjectTOKSİKOLOJİ
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSağlık Bilimleri
dc.subjectEczacılık
dc.subjectMeslek Bilimleri
dc.subjectTarımsal Bilimler
dc.subjectZiraat
dc.subjectGıda Mühendisliği
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectMühendislik ve Teknoloji
dc.titleEffects of 3-monochloropropane-1,2-diol (3-MCPD) and its metabolites on DNA damage and repair under in vitro conditions
dc.typeMakale
dc.relation.journalFOOD AND CHEMICAL TOXICOLOGY
dc.contributor.departmentUniversity of Messina , ,
dc.identifier.volume89
dc.identifier.startpage1
dc.identifier.endpage7
dc.contributor.firstauthorID86503


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