Krasavage W J, Hosenfeld R S, Katz G V
Toxicological Sciences Laboratory, Eastman Kodak Company, Rochester, New York 14652-3615.
Fundam Appl Toxicol. 1990 Oct;15(3):517-27. doi: 10.1016/0272-0590(90)90038-l.
To determine the potential developmental toxicity of ethylene glycol monopropyl ether (EGPE), groups of pregnant New Zealand white rabbits were exposed to target concentrations of 0, 125, 250, or 500 ppm EGPE vapors for 6 hr a day on Days 6-18 of gestation. Maternal effects included a slight reduction in feed consumption during the first week of treatment at the 250- and 500-ppm exposure levels and slightly reduced body weight gain at the 500-ppm level compared to those of the controls, but the differences were not statistically significant. One doe exposed to 500 ppm had red-colored urine during the 24-hr period following the second exposure. Hematologic determinations, absolute and relative organ weights, and observations at necropsy revealed no treatment-related maternal effects. Reproductive indices, i.e., pregnancy rate, number of corpora lutea, implantation sites, viable fetuses, early and late resorptions, fetal body weights, fetal sex ratio, and the gravid uterine and corrected body weights, were not affected by exposures to EGPE. The occurrences of external and internal soft tissue malformations and variations and the incidences of skeletal malformations in the EGPE-exposed groups were not significantly different from those in the control group. Common skeletal variations, in many instances, were seen less frequently in EGPE-exposed fetuses than in control fetuses. In those cases where the incidence of fetuses with a skeletal variation was greater for EGPE-exposed fetuses than that for control fetuses, the number of litters involved was not significantly different from that of the control group. Thus, EGPE vapor concentrations as high as 500 ppm did not produce teratogenicity or other developmental toxicity in the rabbit conceptus.
为确定乙二醇单丙醚(EGPE)的潜在发育毒性,将妊娠的新西兰白兔分组,在妊娠第6至18天每天6小时暴露于目标浓度为0、125、250或500 ppm的EGPE蒸气中。母体效应包括在250 ppm和500 ppm暴露水平下治疗的第一周饲料消耗量略有减少,以及与对照组相比,500 ppm水平下体重增加略有减少,但差异无统计学意义。一只暴露于500 ppm的母兔在第二次暴露后的24小时内尿液呈红色。血液学测定、绝对和相对器官重量以及尸检观察未发现与治疗相关的母体效应。生殖指标,即妊娠率、黄体数、着床部位、活胎数、早期和晚期吸收、胎儿体重、胎儿性别比以及妊娠子宫和校正体重,均不受EGPE暴露的影响。EGPE暴露组的外部和内部软组织畸形及变异的发生率以及骨骼畸形的发生率与对照组无显著差异。在许多情况下,EGPE暴露胎儿中常见的骨骼变异比对照胎儿中少见。在那些EGPE暴露胎儿骨骼变异发生率高于对照胎儿的情况下,涉及的窝数与对照组无显著差异。因此,高达500 ppm的EGPE蒸气浓度未对兔胚胎产生致畸性或其他发育毒性。