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Proc Natl Acad Sci U S A ; 70(5): 1461-3, 1973 May.
Article in English | MEDLINE | ID: mdl-4514315

ABSTRACT

Blood leukocyte cultures were incubated with antioxidants and the carcinogens sodium cyclamate and 7,12-dimethylbenz(alpha)anthracene in different combinations. There were 17.4% more chromosomal breaks in the group of cells treated with dimethylbenzanthracene only than in the untreated controls. The reductions in chromosomal breaks by the antioxidants were as follows: ascorbic acid, 31.7%; butylated hydroxytoluene, 63.8%; Na(2)SeO(3), 42.0%; and dl-alpha-tocopherol, 63.2%. Multiple chromosomal breaks were distributed equally throughout the experimental groups. Sodium cyclamate had only slightly more chromosomal breaks than the controls (11.6 compared to 10.9%). In the cyclamate groups treated with Na(2)SeO(3), 11.2% of chromosomes were broken. More acrocentric-type chromosomal breaks (21.7%) were seen in the untreated cells than the cells treated with cyclamate (3.4%) or dimethylbenzanthracene alone (4.8%). The carcinogen-treated groups had a higher percentage of meta breaks than the untreated controls.


Subject(s)
Antioxidants/pharmacology , Carcinogens/pharmacology , Chromosomes/drug effects , Adult , Ascorbic Acid/pharmacology , Benz(a)Anthracenes/pharmacology , Carcinogens/antagonists & inhibitors , Chromosome Aberrations , Cresols/pharmacology , Cyclamates/pharmacology , Humans , In Vitro Techniques , Lectins/pharmacology , Leukocytes/cytology , Leukocytes/drug effects , Male , Selenium/pharmacology , Sodium/pharmacology , Vitamin E/pharmacology
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