Birgo B B, Bellward G D
Environ Physiol Biochem. 1975;5(6):440-50.
Reproduction was studied in SWV female mice that had raised one litter and then received either 0.2.5,5,10,15,20 or 25 parts/10(6) dietary dieldrin (n = 18 or 19 per group). Exposure began 4 weeks prior to the second mating and continued until day 28 postpartum (weaning). Fertile males were caged with the females during weeks 5-6 of exposure. Significantly mortality of the females occurred only at 20 and 25 parts/10(6) (89% and 56%, respectively) and all deaths occurred before parturition. Dieldrin did not affect behavioural oestrus. At 10 and 15 parts/10(6), 18% of the bred females did not become pregnant; all animals at lower doses and all survivors at higher doses were fertile. The gestation period was not affected. At 25 parts/10(6), the litter size was decreased by 17% over the control size (13.2 pups). The infertility and reduced fecundity resulted from a lesion(s) preceding implantation. Thus, in a separate experiment, 15 parts/10(6) increased the number of bred females that had no implantation sites 5 days post coitum while 25 parts/10(6) decreased the number of sites per pregnant female. As expected from the original dose-responses for infertility and decreased litter size, the converse effects did not occur. Pre-weaning mortality of all the pups occurred in 31%, 47%, 80% and 100% of the litters at 0,2.5,5, and larger than or equal to parts/10(6), respectively. Within the litters raised at 2.5 and 5 parts/10(6), the pup survival was not different from the controls (75%). Thus, in this strain, litter -oss is dieldrin's most important reproductive effect and it correlated with a dieldrin-induced maternal hepatomegaly. The birth weight of pups in litters that were lost was reduced by 3-13% and pre-death growth was reduced or absent. Pup-killing and pup-neglect were important proximate causes of mortality, but only at doses larger than or equal to 15 parts/10(6).
对已生育过一窝幼崽的SWV雌性小鼠的繁殖情况进行了研究,这些小鼠随后分别接受了0、2.5、5、10、15、20或25 ppm(百万分之几)的膳食狄氏剂(每组n = 18或19只)。暴露在第二次交配前4周开始,并持续到产后第28天(断奶)。在暴露的第5 - 6周,将可育雄性与雌性关在同一笼中。仅在20和25 ppm时雌性出现显著死亡率(分别为89%和56%),且所有死亡均发生在分娩前。狄氏剂不影响行为性发情。在10和15 ppm时,18%的已交配雌性未怀孕;较低剂量组的所有动物以及较高剂量组的所有存活动物均具有生育能力。妊娠期未受影响。在25 ppm时,窝仔数比对照组(13.2只幼崽)减少了17%。不育和繁殖力下降是由着床前的损伤引起的。因此,在一项单独实验中,15 ppm增加了交配后5天无着床部位的已交配雌性数量,而25 ppm减少了每只怀孕雌性的着床部位数量。正如不育和窝仔数减少的原始剂量反应所预期的那样,相反的效应并未出现。在0、2.5、5以及大于或等于10 ppm时,所有幼崽的断奶前死亡率分别出现在31%、47%、80%和100%的窝中。在以2.5和5 ppm饲养的窝中,幼崽存活率与对照组(75%)无差异。因此,在该品系中,窝仔数减少是狄氏剂最重要的生殖效应,并且它与狄氏剂诱导的母体肝肿大相关。死亡窝中幼崽的出生体重降低了3% - 13%,死亡前的生长减缓或停止。杀幼崽和忽视幼崽是死亡率的重要直接原因,但仅在大于或等于15 ppm的剂量时出现。