Rogers John M, Brannen Kimberly C, Barbee Brenda D, Zucker Robert M, Degitz Sigmund J
Reproductive Toxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, United States Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA.
Birth Defects Res B Dev Reprod Toxicol. 2004 Apr;71(2):80-8. doi: 10.1002/bdrb.20003.
Exposure of pregnant outbred CD-1 mice to methanol during the period of gastrulation results in exencephaly, cleft palate, and cervical vertebra malformations [Rogers and Mole, Teratology 55: 364, 1997], while inbred C57BL/6J mice are sensitive to the teratogenicity of ethanol. C57BL/6J fetuses exhibit the holoprosencephaly spectrum of malformations after maternal exposure to ethanol during gastrulation, but the sensitivity of C57BL/6J mice to methanol-induced teratogenesis has not been previously described.
Pregnant C57BL/6J mice were administered two i.p. injections totaling 3.4 or 4.9 g/kg methanol or distilled water four hrs apart on gestation day 'GD' 7. On GD 17, litters were examined for numbers of live, dead and resorbed conceptuses, fetuses were weighed as a litter and examined externally, and all fetuses were double stained for skeletal analysis.
No maternal intoxication was apparent, but the high dosage level caused a transient deficit in maternal weight gain. The number of live fetuses per litter was reduced at both dosages of methanol, and fetal weight was lower in the high dosage group. Craniofacial defects were observed in 55.8% of fetuses in the low dosage group and 91.0% of fetuses in the high dosage group, including micro/anophthalmia, holoprosencephaly, facial clefts and gross facial angenesis. Skeletal malformations, particularly of the cervical vertebrae, were observed at both dosages of methanol, and were similar to those previously reported in the CD-1 mouse following methanol exposure.
The types of craniofacial malformations induced in the C57BL/6J mouse by methanol indicate that methanol and ethanol have common targets and may have common modes of action.
在原肠胚形成期,将远交系CD - 1怀孕小鼠暴露于甲醇中会导致无脑畸形、腭裂和颈椎畸形[罗杰斯和莫尔,《致畸学》55: 364,1997],而近交系C57BL / 6J小鼠对乙醇的致畸性敏感。在原肠胚形成期母体暴露于乙醇后,C57BL / 6J胎儿会出现全前脑畸形谱,但此前尚未描述C57BL / 6J小鼠对甲醇诱导致畸作用的敏感性。
在妊娠第7天(GD7),给怀孕的C57BL / 6J小鼠腹腔注射两次甲醇或蒸馏水,两次注射总量分别为3.4或4.9 g / kg,间隔4小时。在GD17时,检查窝仔中活胎、死胎和吸收胎的数量,将一窝胎儿称重并进行外部检查,所有胎儿进行双重染色以进行骨骼分析。
未观察到明显的母体中毒现象,但高剂量组导致母体体重增加出现短暂不足。两个甲醇剂量组的每窝活胎数量均减少,高剂量组的胎儿体重较低。低剂量组55.8%的胎儿和高剂量组91.0%的胎儿出现颅面缺陷,包括小眼/无眼、全前脑畸形、面部裂隙和严重的面部发育不全。两个甲醇剂量组均观察到骨骼畸形,尤其是颈椎畸形,与之前报道的CD - 1小鼠甲醇暴露后的畸形相似。
甲醇在C57BL / 6J小鼠中诱导的颅面畸形类型表明,甲醇和乙醇有共同的靶点,可能有共同的作用模式。