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dc.contributor.authorAkcay, T
dc.contributor.authorOzbay, G
dc.contributor.authorIlkova, H
dc.contributor.authorAlademir, Z
dc.contributor.authorDincer, Y
dc.date.accessioned2021-03-05T08:20:52Z
dc.date.available2021-03-05T08:20:52Z
dc.identifier.citationDincer Y., Akcay T., Ilkova H., Alademir Z., Ozbay G., "DNA damage and antioxidant defense in peripheral leukocytes of patients with type I diabetes mellitus", MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, cilt.527, ss.49-55, 2003
dc.identifier.issn0027-5107
dc.identifier.othervv_1032021
dc.identifier.otherav_9861b829-6c52-470d-a7c5-a7268504893e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/102551
dc.identifier.urihttps://doi.org/10.1016/s0027-5107(03)00073-3
dc.description.abstractWe determined relationship among DNA damage, nitric oxide (NO) and antioxidant defense in leukocytes of patients with Type 1 DM. DNA damage was evaluated as strand breakage and formamidopyrimidine DNA glycosylase (Fpg)-sensitive sites by the comet assay in DNA from leukocytes of the subjects. Nitrite level, as a product of NO, superoxide dismutase (SOD) activity and glutathione peroxidase (G-Px) activity of the leukocytes were measured by spectrophotometric kits. Serum glucose level and glycosylated haemoglobin (HbA(1c)) were higher in the patients, as expected. Differences in measured parameters between controls and patients were assessed in men and women separately. There was no significant difference between patient and control groups in neither men nor women for nitrite level. Strand breakage and Fpg-sensitive sites were found to be increased, SOD and G-Px activities of the leukocytes were found to be decreased in both men and women of patient group as compared to their respective controls. Significant correlations were determined between strand breakage and HbA(1c) (r 0.37, P < 0.05); Fpg-sensitive sites and HbA(1c) (r = 0.59, P < 0.01); Fpg-sensitive sites and glucose (r = 0.45, P < 0.02); Fpg-sensitive sites and SOD (r = -0.48, P < 0.02); HbA(1c), and SOD (r = -0.50, P < 0.02). In conclusion, impaired antioxidant defense in leukocytes of patients with Type I DM may be one of the responsible mechanisms for increased DNA damage in those patients. (C) 2003 Elsevier Science B.V. All rights reserved.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectEczacılık
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectYaşam Bilimleri
dc.subjectBiyoteknoloji
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectTOKSİKOLOJİ
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMikrobiyoloji
dc.subjectBİYOTEKNOLOJİ VE UYGULAMALI MİKROBİYOLOJİ
dc.titleDNA damage and antioxidant defense in peripheral leukocytes of patients with type I diabetes mellitus
dc.typeMakale
dc.relation.journalMUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
dc.contributor.department, ,
dc.identifier.volume527
dc.identifier.startpage49
dc.identifier.endpage55
dc.contributor.firstauthorID168698


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