Teratogenic Effect of Chlormadinone Acetate in Mice and Rabbits
K. Takano, Henry I. Yamamura, M. Suzuki, H. Nishimura
Abstract
K. Takano, Henry I. Yamamura, M. Suzuki, H. Nishimura
Abstract
Oral administration of a large amount of chlormadinone acetate into pregnant mice and rabbits produced a large number of fetal malformations, such as cleft palate and others, while norethisterone with 1% mestranol showed no such teratogenic activity though its lethal effect on the fetuses was stronger than that of chlormadinone acetate. Norethynodrel with 2% mestranol showed the strongest lethal effect of the progestogens tested in mouse embryos, and cleft palate was induced in the surviving fetuses at 10 mg/kg. The dosage of the drugs which showed teratogenicity was generally much higher than human therapeutic or pharmacological doses in rabbits on the basis of maternal body weight.
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Oral administration of a large amount of chlormadinone acetate into pregnant mice and rabbits produced a large number of fetal malformations, such as cleft palate and others, while norethisterone with 1% mestranol showed no such teratogenic activity though its lethal effect on the fetuses was stronger than that of chlormadinone acetate. Norethynodrel with 2% mestranol showed the strongest lethal effect of the progestogens tested in mouse embryos, and cleft palate was induced in the surviving fetuses at 10 mg/kg. The dosage of the drugs which showed teratogenicity was generally much higher than human therapeutic or pharmacological doses in rabbits on the basis of maternal body weight.
Key concepts: Chlormadinone acetate, Mestranol, Fetus, Norethynodrel, Medicine, Norethisterone acetate, Physiology, Internal medicine