Teratogenicity of 13-cis retinoic acid and phenobarbital sodium in CF-1 mice.

M M Yuschak, R F Gautieri
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Abstract

The teratogenicity of 13-cis-retinoic acid (RA) either administered alone or following pretreatment with phenobarbital sodium (PB), was assessed. Groups of gravid CF-1 mice were administered dosages of either 10, 100, 200, or 400 mg/kg of RA orally on either days 11, 12 or 13 of gestation, in order to determine structural alterations. In addition, separate groups of mice were orally pretreated with 80 mg/kg/day of PB on days 7 through 10 of gestation prior to the administration of RA. Skeletal alterations attributed to maternal administration of either 100, 200 or 400 mg/kg of RA on days 11-13 included delayed ossification of the limbs and supraoccipital bone, the presence of extra ribs, and various sternebral defects. Soft tissue alterations included cleft palate and dilation of the renal pelves which occurred following maternal exposure on days 11 and 12-13, respectively. Significant decreases in the incidence of cleft palate and delayed ossification of the limbs were observed in those dams administered RA on days 11 or 12, respectively, following prior treatment with PB. These data suggest that administration of PB, a prototypical hepatic microsomal enzyme inducer, may partially antagonize the teratogenicity of RA.

13-顺式维甲酸和苯巴比妥钠对CF-1小鼠的致畸性。
对13-顺式维甲酸(RA)单独或经苯巴比妥钠(PB)预处理后的致畸性进行了评估。在妊娠第11天、第12天或第13天,对怀孕的CF-1小鼠组口服10、100、200或400 mg/kg的RA,以确定其结构变化。此外,在给药前,各组小鼠在妊娠第7 ~ 10天口服80 mg/kg/天的PB预处理。母亲在第11-13天给予100mg /kg、200mg /kg或400mg /kg类风湿性关节炎导致的骨骼改变包括四肢和枕上骨的延迟骨化、多余肋骨的出现和各种胸骨缺损。软组织改变包括腭裂和肾盂扩张,分别发生在母体暴露后的第11天和第12-13天。在先前的PB治疗后,分别在第11天和第12天给予RA的小鼠,腭裂和肢体延迟骨化的发生率显著降低。这些数据表明,给药PB,一种典型的肝微粒体酶诱导剂,可能部分拮抗RA的致畸性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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