Rees E D, Majumdar S K, Shuck A
Proc Natl Acad Sci U S A. 1970 Aug;66(4):1228-35. doi: 10.1073/pnas.66.4.1228.
Multiple intravenous injections of an emulsion containing 7,12-dimethylbenz(a)anthracene (DMBA) or 7,8,12-trimethylbenz(a)anthracene (TMBA) induce a high incidence of leukemia in rats. Twenty-four hours after a single injection, about half of the metaphase cells in the marrow have chromosomes with breaks. Although breaks were inflicted on chromosomes of various sizes and morphology, these aberrations were nonrandom in that members of the nos. 1 and 2 chromosome pairs were involved to an extent greater than expected on the basis of their size and number. Distinctive karyotypic abnormalities involving the no. 2 chromosome were observed in half of the leukemic rats, whereas these abnormalities were not observed in nonleukemic, DMBA-treated rats. Benzo(a)pyrene and benzo(e)pyrene, polycyclic aromatic hydrocarbons which did not induce leukemia, produced fewer breaks of the no. 2 (and other) chromosomes than did DMBA or TMBA.
多次静脉注射含有7,12 - 二甲基苯并(a)蒽(DMBA)或7,8,12 - 三甲基苯并(a)蒽(TMBA)的乳剂可在大鼠中诱发高发病率的白血病。单次注射后24小时,骨髓中约一半的中期细胞染色体出现断裂。尽管断裂发生在各种大小和形态的染色体上,但这些畸变并非随机发生,因为1号和2号染色体对的成员受累程度大于根据其大小和数量所预期的程度。在一半的白血病大鼠中观察到涉及2号染色体的独特核型异常,而在未患白血病的DMBA处理大鼠中未观察到这些异常。苯并(a)芘和苯并(e)芘这两种不诱发白血病的多环芳烃,与DMBA或TMBA相比,导致2号(及其他)染色体断裂的情况较少。