Webster W S, Germain M A, Lipson A, Walsh D
Cardiovasc Res. 1984 Jun;18(6):335-8. doi: 10.1093/cvr/18.6.335.
Pregnant mice were exposed to a single dose of alcohol (0.03 ml of 25% alcohol X g-1 mouse) or two doses (2 X 0.015 ml of 25% alcohol X g-1 mouse) 4 h apart, by intraperitoneal injection or by gavage, on days 7, 8, 9 or 10 of gestation. The mice were killed on the day before term and the fetuses examined for heart defects. Alcohol exposure on day 8, 9 or 10 of gestation caused a high incidence of ventricular septal defects (60%, 75% and 15% respectively). Defects of both the membranous and muscular parts of the septum were seen as well as more complex ventricular septal defects involving the great vessels. Day 7 was resistant to the induction of heart defects. This study has demonstrated that a relatively short exposure to high doses of alcohol during pregnancy in mice can cause congenital heart defects. This has important implications both as a possible cause of congenital heart anomalies in humans and for the counselling of mothers of affected children.
妊娠第7、8、9或10天,通过腹腔注射或灌胃,给怀孕小鼠单次注射一剂酒精(0.03毫升25%酒精/克小鼠)或两剂(2×0.015毫升25%酒精/克小鼠),两剂间隔4小时。在足月前一天处死小鼠,检查胎儿是否有心脏缺陷。妊娠第8、9或10天暴露于酒精会导致室间隔缺损的高发生率(分别为60%、75%和15%)。可见隔膜膜部和肌部的缺损以及涉及大血管的更复杂的室间隔缺损。第7天对心脏缺陷的诱导具有抗性。这项研究表明,小鼠孕期相对短时间暴露于高剂量酒精会导致先天性心脏缺陷。这对于人类先天性心脏异常的可能原因以及为受影响儿童的母亲提供咨询都具有重要意义。