Tomatis L, Hilfrich J, Turusov V
Int J Cancer. 1975 Mar 15;15(3):385-90. doi: 10.1002/ijc.2910150304.
N-nitrosomethylurea (NMU) was administered once IP at a dose of 20 mg/kg to BD female rats on the 18th day of pregnancy. The first generation descendants (F1) were mated to produce a second generation (F2), which were then mated to produce a third generation (F3). While F1 rats were exposed directly to NMU during intrauterine life, it can be reasonably excluded that F2 and F3 descendants were exposed to NMU or its metabolites. F2 and F3 rats received no other treatment and untreated rats served as controls. Kidney and nervous-tissue tumours were observed in F1 descendants and, with a lower incidence, in F2 descendants. In F3 rats, tumours of nervous tissue, but not of kidneys, were observed. These results confirm previous observations that exposure to a carcinogen during prenatal life results in an increased cancer risk which may persist for more than one generation.
在妊娠第18天,以20毫克/千克的剂量对BD雌性大鼠腹腔注射一次N-亚硝基甲基脲(NMU)。第一代后代(F1)进行交配产生第二代(F2),然后F2再进行交配产生第三代(F3)。虽然F1大鼠在子宫内生活期间直接接触了NMU,但可以合理排除F2和F3后代接触了NMU或其代谢产物的可能性。F2和F3大鼠未接受其他治疗,未处理的大鼠作为对照。在F1后代中观察到肾和神经组织肿瘤,F2后代中的发生率较低。在F3大鼠中,观察到神经组织肿瘤,但未观察到肾肿瘤。这些结果证实了先前的观察结果,即产前接触致癌物会导致癌症风险增加,且这种风险可能会持续不止一代。