Fabricant J D, Legator M S, Adams P M
Mutat Res. 1983 Feb;119(2):185-90. doi: 10.1016/0165-7992(83)90127-6.
Transmission of the effects of paternal pre-fertilization exposure to a genotoxic drug being manifested in the F1 progeny is well established using the traditional rodent dominant lethal protocol [7]. More recently, the induction of genotoxic effects in the F1 progeny following chronic paternal exposure prior to fertilization has been described in rats using behavioral testing as an endpoint [1]. In our initial study, male F344 adult rats were treated chronically with 10 mg/kg cyclophosphamide (CP) or saline for 5 weeks (5 days of daily treatment and 2 days of rest). The present study describes the behavior of progeny whose fathers were treated with a single intraperitoneal injection of 10 mg/kg CP and mated at different times post-injection. This design showed that post-meiotic germ cells are the most sensitive to the effects of CP as seen by behavioral testing of the F1 progeny.
利用传统的啮齿动物显性致死试验方案,已经充分证实了父本受精前暴露于基因毒性药物的效应会在F1代子代中显现出来[7]。最近,在大鼠中,以行为测试作为终点,描述了受精前父本长期暴露后F1代子代中基因毒性效应的诱导情况[1]。在我们的初步研究中,成年雄性F344大鼠连续5周每天接受10 mg/kg环磷酰胺(CP)或生理盐水治疗(每天治疗5天,休息2天)。本研究描述了其父本接受单次腹腔注射10 mg/kg CP并在注射后不同时间交配的子代的行为。该设计表明,通过对F1代子代的行为测试可以看出,减数分裂后生殖细胞对CP的影响最为敏感。