Ema M, Miyawaki E, Kawashima K
National Institute of Health Sciences, Osaka Branch, Japan.
Reprod Toxicol. 1998 Mar-Apr;12(2):127-32. doi: 10.1016/s0890-6238(97)00127-5.
In our previous studies, butyl benzyl phthalate (BBP) was found to be embryolethal and teratogenic in rats. In this study, the reproductive effects of BBP were investigated in pregnant and pseudopregnant rats. Rats were given BBP by gastric intubation at 0, 250, 500, 750, or 1000 mg/kg on Days 0 to 8 of pregnancy and the pregnancy outcome was determined on Day 20 of pregnancy. The same doses of BBP were given to pseudopregnant rats, with an induced decidual cell response on Days 0 to 8 of pseudopregnancy, and the uterine weight on Day 9 served as an index of the uterine decidualization. BBP caused significant increases in the incidences of preimplantation loss in females successfully mated at 1000 mg/kg and of postimplantation loss in females having implantations at 750 mg/kg and above. Uterine decidual growth in pseudopregnant rats was significantly decreased at 750 mg/kg and above. These findings suggest that early embryonic loss due to BBP may be mediated, at least in part, via the suppression of uterine decidualization, an impairment of uterine function.
在我们之前的研究中,发现邻苯二甲酸丁苄酯(BBP)对大鼠具有胚胎致死性和致畸性。在本研究中,对怀孕和假孕大鼠的BBP生殖效应进行了研究。在妊娠第0至8天,通过胃内插管给大鼠分别给予0、250、500、750或1000mg/kg的BBP,并在妊娠第20天确定妊娠结局。给假孕大鼠给予相同剂量的BBP,在假孕第0至8天诱导蜕膜细胞反应,并将第9天的子宫重量作为子宫蜕膜化的指标。BBP导致成功交配的雌性大鼠在1000mg/kg剂量下着床前丢失的发生率显著增加,以及在750mg/kg及以上剂量下有着床的雌性大鼠着床后丢失的发生率显著增加。在750mg/kg及以上剂量下,假孕大鼠的子宫蜕膜生长显著降低。这些发现表明,BBP导致的早期胚胎丢失可能至少部分是通过抑制子宫蜕膜化(一种子宫功能损害)介导的。