癌变·畸变·突变
癌變·畸變·突變
암변·기변·돌변
CARCINOGENSES,TERATOGENSIS AND MUTAGENESIS
2014年
3期
225-227
,共3页
黄超培%傅伟忠%王彦武%何励%张洁宏%彭亮
黃超培%傅偉忠%王彥武%何勵%張潔宏%彭亮
황초배%부위충%왕언무%하려%장길굉%팽량
红丝线草%大鼠%胎毒性%致畸性
紅絲線草%大鼠%胎毒性%緻畸性
홍사선초%대서%태독성%치기성
peristrophe roxburghiana%rat%embryo toxicity%teratogenicity
目的:检测红丝线草的致畸性。方法:红丝线草提取液设10.0、5.0、2.5 g/kg 3个剂量组,同时以去离子水作阴性对照,阿司匹林(0.3 g/kg)作阳性对照。每组12只SD孕鼠,受孕6 d开始按10 mL/kg给孕鼠灌胃受试溶液,每天1次,至受孕15 d,共灌胃10次。于妊娠20 d解剖孕鼠,检查胎鼠的身体、外观、内脏及骨骼发育等指标。结果:红丝线草各剂量组的孕鼠体质量、窝质量、胎鼠体质量、身长、尾长、活胎率、吸收胎率及死胎率与阴性对照组比较差异均无统计学意义(P均>0.05),未见胎鼠外观、内脏和骨骼发育异常及畸形。结论:在本实验条件下,红丝线草对大鼠无母体毒性、胚胎毒性和致畸性。
目的:檢測紅絲線草的緻畸性。方法:紅絲線草提取液設10.0、5.0、2.5 g/kg 3箇劑量組,同時以去離子水作陰性對照,阿司匹林(0.3 g/kg)作暘性對照。每組12隻SD孕鼠,受孕6 d開始按10 mL/kg給孕鼠灌胃受試溶液,每天1次,至受孕15 d,共灌胃10次。于妊娠20 d解剖孕鼠,檢查胎鼠的身體、外觀、內髒及骨骼髮育等指標。結果:紅絲線草各劑量組的孕鼠體質量、窩質量、胎鼠體質量、身長、尾長、活胎率、吸收胎率及死胎率與陰性對照組比較差異均無統計學意義(P均>0.05),未見胎鼠外觀、內髒和骨骼髮育異常及畸形。結論:在本實驗條件下,紅絲線草對大鼠無母體毒性、胚胎毒性和緻畸性。
목적:검측홍사선초적치기성。방법:홍사선초제취액설10.0、5.0、2.5 g/kg 3개제량조,동시이거리자수작음성대조,아사필림(0.3 g/kg)작양성대조。매조12지SD잉서,수잉6 d개시안10 mL/kg급잉서관위수시용액,매천1차,지수잉15 d,공관위10차。우임신20 d해부잉서,검사태서적신체、외관、내장급골격발육등지표。결과:홍사선초각제량조적잉서체질량、와질량、태서체질량、신장、미장、활태솔、흡수태솔급사태솔여음성대조조비교차이균무통계학의의(P균>0.05),미견태서외관、내장화골격발육이상급기형。결론:재본실험조건하,홍사선초대대서무모체독성、배태독성화치기성。
OBJECTIVE:To determine the teratogenic effects of peristrophe roxburghiana (Schult.) brem in rats. METHODS:Pregnant rats were divided into 5 groups,each with 12 rats. Three groups were treated orally with th thexract from peristrophe roxburghiana for 10 days from 6 to 15 day of pregnancy with doses of 10.0,5.0,2.5 g/kg. The other two groups were fed orally with deionized water as negative control and aspirin with 0.3 g/kg as positive control. At th20 day,the rats were sacrificed to allow physical examination of the fetuses. RESULTS:In all treated groups the body weight of parental rats, litter weight, live rate, fetus body weight and fetus length were not significantly different from negative control group (P>0.05),and no abnormality of organ or external was found in the fetuses. CONCLUSION:In these experimental conditions,peristrophe roxburghiana had no appearance maternal toxicity,embryo toxicity nor teratogenicity in rats.