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Development of a metabolic activation system for the frog embryo teratogenesis assay:Xenopus(FETAX)

机译:青蛙胚胎致畸试验代谢活化系统的开发:非洲爪蟾(FETAX)

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AbstractFETAX (frog embryo teratogenesis assay:Xenopus) is a 96‐hr teratogenesis screening assay using embryos of the South African clawed frog,Xenopus laevis.SinceXenopusembryos have limited xenobiotic metabolism through 96 hr of development, we have developed an in vitro metabolic activation system employing Aroclor 1254‐induced rat liver microsomes. By adding an exogenous source of mixed functional oxidase (MFO) activity, we may more accurately assess the teratogenic risk of proteratogenic compounds.Xenopusembryos were cocultured with varying concentrations of cyclophosphamide (CP), Aroclor 1254‐induced microsomal protein, an NADPH‐generating system, and antibiotics in a static renewal fashion for 96 hr. Residual Aroclor 1254 remaining in the microsomes was successfully reduced during purification to levels that had no significant effect on embryo survival and development. The results of three definitive dose‐response tests performed with CP revealed that activation reduced the 96 hr LC50from 8.0 to 1.4 mg/ml (5.7‐fold). The 96‐hr EC50(malformation) was reduced from 6.2 to 0.4 mg/ml (15.5‐fold). Activation also increased the types and severity of malformation and reduced embryonic growth. Aroclor 1254‐induced rat liver microsomes may be used as an acceptable in vitro metabolic activation
机译:摘要FETAX(frog embryo teratogenesis assay:Xenopus)是一种使用南非爪蛙(Xenopus laevis)胚胎进行96小时致畸筛选试验。由于非洲爪蟾胚胎在96小时的发育过程中具有有限的异种代谢,因此我们开发了一种采用Aroclor 1254诱导的大鼠肝微粒体的体外代谢激活系统。通过添加混合功能氧化酶(MFO)活性的外源性来源,我们可以更准确地评估致畸化合物的致畸风险。非洲爪蟾胚胎与不同浓度的环磷酰胺 (CP)、Aroclor 1254 诱导的微粒体蛋白、NADPH 生成系统和抗生素以静态更新方式共培养 96 小时。使用 CP 进行的三项确定性剂量反应测试的结果显示,激活将 96 小时 LC50 从 8.0 降低到 1.4 mg/ml(5.7 倍)。96 小时 EC50(畸形)从 6.2 mg/ml 降低到 0.4 mg/ml(15.5 倍)。活化还增加了畸形的类型和严重程度,并减少了胚胎生长。Aroclor 1254诱导的大鼠肝微粒体可用作可接受的体外代谢激活

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