Nagao T, Saito Y, Watanabe C, Imai K
Laboratory of Reproductive and Developmental Toxicology, Hatano Research Institute, Kanagawa, Japan.
Reprod Toxicol. 1997 Jan-Feb;11(1):37-45. doi: 10.1016/s0890-6238(96)00195-5.
5-Bromo-2'-deoxyuridine (BrdU) was administered intraperitoneally to Sprague-Dawley rats at doses of 12.5, 25, 50, or 100 mg/kg/d on days 9 through 15 of gestation, and at 50 or 100 mg/kg/d on days 16 through 20 of gestation. Dams were allowed to deliver naturally and the numbers of live and dead pups were recorded. Male offspring were allowed to mature and then cohabited with untreated female rats for assessment of reproductive performance. Dam body weight gain during pregnancy and lactation periods was not reduced by the treatment with BrdU. Dams treated with 50 and 100 mg BrdU/kg on days 9 through 15 of gestation had litters with decreased survival rates. The male offspring from dams treated with 25, 50, and 100 mg BrdU/kg on days 9 through 15 of gestation had reduced body weights over the course of the entire study. A dose-related decrease in copulation and fertility rates was found in the male offspring of dams treated on days 9 through 15 of gestation, while no significant decrease in those rates were found in the male offspring of dams treated on days 16 through 20 of gestation. Neither histopathologic examination of testes nor sperm examination indicated the cause of the impaired fertility in the male offspring from dams treated with BrdU on days 9 through 15 of gestation. All of the male offspring of dams treated with 100 mg BrdU/kg on days 9 through 15 of gestation failed to copulate, and some of the male offspring of dams treated with 50 mg BrdU/kg on days 9 through 15 of gestation did not form copulatory plugs or formed very small plugs. Dilatation of the lateral ventricles and cysts in the pars distalis of the pituitary were observed in all of the male offspring of dams treated with 100 mg BrdU/kg on days 9 through 15 of gestation. The impaired fertility of the male offspring of dams treated prenatally with BrdU may have resulted from BrdU exposure effects on central nervous system action such as loss of libido and from failure to form proper copulatory plugs, rather than the direct effects of BrdU on the male reproductive organs.
在妊娠第9至15天,以12.5、25、50或100毫克/千克/天的剂量给斯普拉格-道利大鼠腹腔注射5-溴-2'-脱氧尿苷(BrdU);在妊娠第16至20天,以50或100毫克/千克/天的剂量注射。让母鼠自然分娩,并记录活仔和死仔的数量。雄性后代成熟后与未经处理的雌性大鼠同居,以评估生殖性能。BrdU处理并未降低母鼠在怀孕和哺乳期的体重增加。在妊娠第9至15天接受50和100毫克BrdU/千克处理的母鼠所产仔鼠的存活率降低。在整个研究过程中,妊娠第9至15天接受25、50和100毫克BrdU/千克处理的母鼠所产雄性后代体重减轻。在妊娠第9至15天接受处理的母鼠所产雄性后代的交配率和生育率呈剂量相关下降,而在妊娠第16至20天接受处理的母鼠所产雄性后代中未发现这些比率有显著下降。对睾丸的组织病理学检查和精子检查均未表明妊娠第9至15天接受BrdU处理的母鼠所产雄性后代生育力受损的原因。在妊娠第9至15天接受100毫克BrdU/千克处理的母鼠所产的所有雄性后代均未能交配,在妊娠第9至15天接受50毫克BrdU/千克处理的母鼠所产的一些雄性后代未形成交配栓或形成的交配栓非常小。在妊娠第9至15天接受100毫克BrdU/千克处理的母鼠所产的所有雄性后代中均观察到侧脑室扩张和垂体远侧部囊肿。产前接受BrdU处理的母鼠所产雄性后代生育力受损可能是由于BrdU暴露对中枢神经系统作用(如性欲丧失)的影响以及未能形成合适的交配栓,而不是BrdU对雄性生殖器官的直接影响。