Shah R M
J Anat. 1979 Oct;129(Pt 3):531-9.
Development of the palate was studied in normal and triamcionolone-treated hamster fetuses. The results demonstrated that normal palatogenesis was completed between days 12 and 13 of gestation. Following triamcinolone treatment the reorientation of the palatal shelves was delayed before there was any general retardation of fetal growth (as indicated by crown-rump length and body weight). Since triamcinolone affected palatogenesis at an earlier stage than hydrocortisone, the view that the former is a more potent teratogen was supported. Chronological age, fetal weight and crown-rump length were reliable predictors of normal palatogenesis in the hamster, whereas the numerical morphological rating systems were not. Neither measures of general fetal growth, nor numerical rating, were useful in predicting the stages of experimentally induced cleft palate, since triamcinolone appears to be site-specific, and the drug does not produce a general retardation of embryonic development.
在正常和经曲安奈德处理的仓鼠胎儿中研究了腭的发育。结果表明,正常的腭发生在妊娠第12至13天之间完成。经曲安奈德处理后,在胎儿生长出现任何总体迟缓(以顶臀长度和体重表示)之前,腭板的重新定向就已延迟。由于曲安奈德比氢化可的松更早地影响腭发生,这支持了前者是一种更强效致畸剂的观点。在仓鼠中,按时间顺序的年龄、胎儿体重和顶臀长度是正常腭发生的可靠预测指标,而数字形态评分系统则不是。总体胎儿生长指标和数字评分都无助于预测实验诱导腭裂的阶段,因为曲安奈德似乎具有部位特异性,并且该药物不会导致胚胎发育的总体迟缓。