作者: H. K. Cooper , E. Hauenstein , G. F. Kolar , P. Kleihues
DOI: 10.1007/BF00685004
关键词:
摘要: The role of DNA alkylation by the neurooncogenic agent 3,3-dimethyl-1-phenyltriazene (DMPT) was investigated perinatally and in adult rats. Following a single subcutaneous injection of14C-DMPT (100 mg/kg) on 21st day gestation, concentration methylated purines similar both fetal liver brain whereas during postnatal growth this treatment resulted an increasingly preferential methylation DNA. In 30-day-old rats 7-methylguanine about 8 times higher DNA, suggesting that prenatal development are transplacentally proximate carcinogen produced maternal organs. Multiple doses (50 to led accumulation O6-methylguanine cerebral This supports hypothesis deficient repair excision capacity central nervous system is significant factor organ-specific carcinogenicity DMPT related carcinogens.