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机构地区:[1]浙江医科大学药学系药理学教研室
出 处:《癌变.畸变.突变》1996年第1期25-28,共4页Carcinogenesis,Teratogenesis & Mutagenesis
摘 要:SD大鼠于妊娠d15到仔鼠出生后PN22连续im抗孕唑0.01和0.2mg/kg,另设溶剂对照和甲巯基咪唑阳性对照,对仔鼠作出牙和开眼时间、平面翻正、斜坡转身、听觉惊愕、游泳、开旷场地和Y型水迷宫试验。结果,抗孕唑高剂量组仔鼠体重明显低于活剂组;低剂量组仔鼠长齿时间(10.6±0.7d)和高剂量组开眼时间(13.6±0.9d)较溶剂组(11.4±1.2,15.3±1.0d)提前,其他指标均无明显改变。阳性对照组多项指标改变显著。因此,抗孕唑在抗早孕阈下剂量时,对仔鼠无功能畸变作用。Groups of pregnant Sprague-Dawley rats were treated with im 0.01 and 0.2mg/kg of contragcstazol(DL111-IT)from gestational day 15 to postnatal day 22,methimazol indrinking water served as positive control.The results showed that there were no marked dif- ferences in surface righting,negative geotaxis,auditory startle,swimming ontogeriy,openfield and water Y-maze between test and vehiele groups. However,the body weight of theoffsprings from rats tred,ted with 0.2mg/kg of contragestazol was significantly reduced.Me-thimazol,a positive control agent,not only caused delay of certain physical development,butalso caused deficits of some behaviors.It was concluded that contragestazol,at dosages belowterminating early pregnancy,did not induce behavioral teratogcnicity of offsprings.
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