氟嗪酸的小鼠胚胎毒性及致畸性研究  被引量:1

EMBRYOTOXICITY AND TERATOGENICITY STUDY OFOFLOXACIN IN NIH MICE

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作  者:朱永平[1] 王敏[1] 倪祖敏[1] 滕素珍 

机构地区:[1]浙江医科大学毒理研究室

出  处:《癌变.畸变.突变》1996年第1期28-31,共4页Carcinogenesis,Teratogenesis & Mutagenesis

摘  要:NIH小鼠于孕期d6—15po氟嗪酸2100、700mg/kg,结果高剂量的氟嗪酸使NIH孕鼠增重减少,透过胎盘屏障影响胎鼠的生长发育,胎鼠的身长和体重均显著低于溶剂对照组,枕骨和胸骨发育不良率显著增高,颚裂的发生率有增高的趋势。因此临床上应避免给怀孕和哺乳的妇女以及儿童使用该类药物。The embryotoxicity and teratogenicity of ofloxacin in NIH mice were carried out.Ofloxacin was administered at 2100,700mg/kg po on day 6-15 of the gestation, As com-pared to the solvent control,high dosge of ofloxacin(2100 mg/kg ,about 1/3 LD50)was tox-ic to pregnant mice,resulted in reduction of the weight gain during the pregnancy and embry-otoxicity.The body length and weight of survial fetuses in the higher dose group is less andthe percentage of delayed skeletogency is higher than others.No malformation of survial fe-tuses was observed in every group but the percentage of platoschisis in the higher dosegroup tended to be increased.These studies indicated that ofloxacin is embryotoxic but notteratogenic in NIH mice.

关 键 词:氟嗪酸 小鼠 胚胎毒性 致畸性 

分 类 号:R978.19[医药卫生—药品]

 

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