Age-dependent oxidative stress-induced DNA damage in Down's lymphocytes
Creators
- 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
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38027319
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- AGE DEPENDENCE; BIOLOGICAL STRESS; CHILDREN; DAMAGE; DNA; DNA REPAIR; DOWNS SYNDROME; HYDROGEN PEROXIDE; IN VITRO; LYMPHOCYTES; PURINES; PYRIMIDINES; STRAND BREAKS
- Descriptors DEC
- AGE GROUPS; ANIMAL CELLS; ANIMALS; AROMATICS; AZAARENES; AZINES; BIOLOGICAL MATERIALS; BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; BLOOD; BLOOD CELLS; BODY FLUIDS; CONGENITAL DISEASES; CONGENITAL MALFORMATIONS; CONNECTIVE TISSUE CELLS; DISEASES; DNA DAMAGES; HEREDITARY DISEASES; HETEROCYCLIC COMPOUNDS; HYDROGEN COMPOUNDS; LEUKOCYTES; MALFORMATIONS; MAMMALS; MAN; MATERIALS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; PATHOLOGICAL CHANGES; PEROXIDES; PRIMATES; REPAIR; SOMATIC CELLS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.