Published June 30, 2006 | Version v1
Journal article

Age-dependent oxidative stress-induced DNA damage in Down's lymphocytes

  • 1. Department of Psychiatry, Alzheimer's Disease Research Center, Faculty of Medicine, Albert Szent-Gyoergyi Center for Medical and Pharmaceutical Sciences, University of Szeged, 6 Semmelweis St., Szeged, H-6725 (Hungary)
  • 2. Biological Research Center of Hungarian Academy of Sciences, Institute of Genetics, 62 Temesvari St., Szeged, H-6726 (Hungary)
  • 3. Department of Child and Adolescent Psychiatry, Faculty of Medicine, Albert Szent-Gyoergyi Center for Medical and Pharmaceutical Sciences, University of Szeged, 6 Semmelweis St., Szeged, H-6725 (Hungary)
  • 4. Children's Medical Home, 45 Agyagos St., Szeged, H-6723 (Hungary)
  • 5. Department of Pediatrics, Faculty of Medicine, Albert Szent-Gyoergyi Center for Medical and Pharmaceutical Sciences, University of Szeged, 14-15 Koranyi St., Szeged, H-6720 (Hungary)
  • 6. Department of Medical Informatics, Faculty of Medicine, Albert Szent-Gyoergyi Center for Medical and Pharmaceutical Sciences, University of Szeged, 9 Koranyi St., Szeged, H-6720 (Hungary)

Description

The aim of the present study was to investigate the oxidative status of lymphocytes from children (n = 7) and adults (n = 18) with Down's syndrome (DS). The basal oxidative condition, the vulnerability to in vitro hydrogen peroxide exposure, and the repair capacity were measured by means of the damage-specific alkaline comet assay. Significantly and age-independently elevated numbers of single strand breaks and oxidized bases (pyrimidines and purines) were found in the nuclear DNA of the lymphocytes in the DS group in the basal condition. These results may support the role of an increased level of endogenous oxidative stress in DS and are similar to those previously demonstrated in Alzheimer's disease. In the in vitro oxidative stress-induced state, a markedly higher extent of DNA damage was observed in DS children as compared with age- and gender-matched healthy controls, suggesting that young trisomic lymphocytes are more sensitive to oxidative stress than normal ones. However, the repair ability itself was not found to be deteriorated in either DS children or DS adults

Additional details

Identifiers

DOI
10.1016/j.bbrc.2006.04.167;
PII
S0006-291X(06)01015-1;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
345
Journal Issue
2
Journal Page Range
p. 726-733
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.