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使用灌注大鼠肝脏作为非遗传毒性致癌物早期预测分析方法的体内-体外复制性DNA合成(RDS)试验:I. 标准方案的建立

In vivo-in vitro replicative DNA synthesis (RDS) test using perfused rat livers as an early prediction assay for nongenotoxic hepatocarcinogens: I. Establishment of a standard protocol.

作者信息

Uno Y, Takasawa H, Miyagawa M, Inoue Y, Murata T, Ogawa M, Yoshikawa K

机构信息

Toxicology Laboratory, Mitsubishi Kasei Co., Yokohama, Japan.

出版信息

Toxicol Lett. 1992 Nov;63(2):191-9. doi: 10.1016/0378-4274(92)90011-8.

Abstract

To establish a standard protocol for an in vivo-in vitro hepatocyte replicative DNA synthesis (RDS) test using male F344 rats for screening nongenotoxic (the Ames-negative) hepatocarcinogens, experimental conditions were examined. After treatment with three model hepatocarcinogens, isolated hepatocytes showed highest RDS incidences when plated at a density of 5 x 10(4) cells/ml. Spontaneous RDS incidences in hepatocytes from rats aged 9 weeks or older showed a constant value. The use of hepatocytes from 9-week-old rats at the 5 x 10(4) cells/ml plating density was therefore determined as the standard. Based on the distribution of mean spontaneous RDS incidences over 105 additional experiments (0.4 +/- 0.18%, with SEM), an RDS incidence of over 1% was adopted as the criterion for a positive response in our rat liver RDS test.

摘要

为建立一种使用雄性F344大鼠进行体内-体外肝细胞复制性DNA合成(RDS)试验的标准方案,以筛选非遗传毒性(Ames试验阴性)的肝癌致癌物,对实验条件进行了研究。在用三种模型肝癌致癌物处理后,分离的肝细胞以5×10⁴个细胞/毫升的密度接种时,显示出最高的RDS发生率。9周龄及以上大鼠的肝细胞自发RDS发生率呈现恒定值。因此,确定使用9周龄大鼠的肝细胞,以5×10⁴个细胞/毫升的接种密度作为标准。基于另外105次实验中平均自发RDS发生率的分布(0.4±0.18%,标准误),在我们的大鼠肝脏RDS试验中,将RDS发生率超过1%作为阳性反应的标准。

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