ASSESSMENT OF SMOKING-INDUCED DNA-DAMAGE IN LYMPHOCYTES OF SMOKING MOTHERS OF NEWBORN-INFANTS USING THE ALKALINE SINGLE-CELL GEL-ELECTROPHORESIS TECHNIQUE

Citation
S. Sardas et al., ASSESSMENT OF SMOKING-INDUCED DNA-DAMAGE IN LYMPHOCYTES OF SMOKING MOTHERS OF NEWBORN-INFANTS USING THE ALKALINE SINGLE-CELL GEL-ELECTROPHORESIS TECHNIQUE, Mutation research. Section on environmental mutagenesis and related subjects, 335(3), 1995, pp. 213-217
Citations number
11
Categorie Soggetti
Genetics & Heredity","Environmental Sciences
ISSN journal
01651161
Volume
335
Issue
3
Year of publication
1995
Pages
213 - 217
Database
ISI
SICI code
0165-1161(1995)335:3<213:AOSDIL>2.0.ZU;2-O
Abstract
The single-cell gel electrophoretic (SCGE) technique for detecting the presence of DNA strand breaks and alkali-labile damage in individual cells was used to examine the effect on newborn infants of maternal ex posure to cigarette smoke. The levels of DNA damage in the lymphocytes of 21 newborns of mothers with different smoking habits were compared to those in 10 newborn infants whose mothers had never smoked and 8 n ewborns whose mothers were passively exposed for at least 40 h per wee k in the workplace and home. DNA damage was undetected in lymphocytes of newborns of passively exposed mothers or newborns with mothers of l ow smoking habit by conditions allowing 40 min DNA unwinding and 40 mi n electrophoresis. Presumably longer times were needed for lower level s of damage to be detected by SCGE. The mean length of DNA migration i n lymphocytes between the newborns of smoking mothers did not show any significance but the percentage of damaged cells increased with the f requency of smoking when assessed by non-parametric Mann-Whitney U tes t. The results of SCGE were compared with our results published in the same individuals of sister-chromatid exchange (SCE) frequency. The re sults show similar trends with mean measures of DNA damage increasing with frequency and long history of maternal smoking. These observation s encourage the application of SCGE as a sensitive and useful techniqu e for quantitating DNA damage in individual cells.