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dc.contributor.authorAğalar, Canan
dc.contributor.authorÖZÇAĞLI, EREN
dc.contributor.authorİzdeş, Seval
dc.contributor.authorBaşar, Halil
dc.contributor.authorŞardaş, Semra
dc.contributor.authorKaymak, Çetin
dc.contributor.authorKadıoğlu, Ela
dc.contributor.authorOsmanoğlu, Gökhan
dc.date.accessioned2021-03-05T08:08:50Z
dc.date.available2021-03-05T08:08:50Z
dc.date.issued2008
dc.identifier.citationKaymak Ç., Kadıoğlu E., ÖZÇAĞLI E., Osmanoğlu G., İzdeş S., Ağalar C., Başar H., Şardaş S., "Oxidative DNA damage and total antioxidant status in rats during experimental gram-negative sepsis", HUMAN & EXPERIMENTAL TOXICOLOGY, cilt.27, ss.485-491, 2008
dc.identifier.issn0960-3271
dc.identifier.otherav_976ee9f2-dbf9-4359-859f-67f08e1abc9a
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101928
dc.identifier.urihttps://doi.org/10.1177/0960327108088972
dc.description.abstractSepsis and septic shock remains as leading cause of death in adult intensive care units. It is widely accepted that gram-negative bacteria and their endotoxins cause sepsis and septic shock, predominantly. Enhanced generation of reactive oxygen species may be responsible for tissue injury in septic shock and endotoxemia. The aim of this study was to assess oxidative DNA damage and the total antioxidant status (TAS) in peripheral lymphocytes of rats during different intraperitoneal gram-negative sepsis stages. Adult male Sprague-Dawley rats were divided randomly into four groups. Control group was intraperitoneally inoculated with 2 ml, of pyrogene-free saline (Group I, n = 6), and the other rats received an intraperitoneal inoculum with 2 ml, of saline containing 2 x 10(8) CFU of Escherichia coli. The animals were killed at time zero (Group 1, n = 6), at 6th (Group 11, n = 7), 12th (Group M, n = 7), and 24th (Group IV, n = 7) hour after the E. coli inoculation. Oxidative DNA damage in peripheral lymphocytes of rats was evaluated by modified comet assay (single-cell gel electrophoresis). Formamido-pyrimidine DNA glycosylase (Fpg) and Endonuclease III (Endo III) were used to detect oxidized purines and pyrimidines, respectively. Total antioxidant quantification was carried out using ABTS+ (2,2'-Azino-di-[3 ethyl-benzthiazoline sulphonate]) radical formation kinetics (Randox kit) in serum samples. Significant elevations of basal levels of strand breaks (SB) in Group IV were observed as compared with Group I, II, and III. There was a significant increase in Fpg sites in Group III as compared with Group I and II. However, there was no significant difference in terms of Endo III sites in any of the groups. Although the TAS was decreased with the stages of sepsis, this moderate decrease was significant in only Group IV as compared with Group I. There was no statistically significant correlation between DNA damage and TAS for any of the groups.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectEczacılık
dc.subjectYaşam Bilimleri
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTOKSİKOLOJİ
dc.titleOxidative DNA damage and total antioxidant status in rats during experimental gram-negative sepsis
dc.typeMakale
dc.relation.journalHUMAN & EXPERIMENTAL TOXICOLOGY
dc.contributor.departmentKırıkkale Üniversitesi , ,
dc.identifier.volume27
dc.identifier.issue6
dc.identifier.startpage485
dc.identifier.endpage491
dc.contributor.firstauthorID596879


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