O'Hara T M, Sheppard M A, Clarke E C, Borzelleca J F, Gennings C, Condie L W
Dept. of Pharmacology and Toxicology, Medical College of Virginia, Richmond 23298.
J Appl Toxicol. 1991 Apr;11(2):147-54. doi: 10.1002/jat.2550110214.
The purpose of this study was to evaluate an isolated hepatocyte model for predicting the in vivo hepatotoxicity of carbon tetrachloride (CCl4) and chloroform (CHCl3), alone and in combination. Response surface methodology (RSM) was used to analyze and describe the data. The interaction was evaluated for % initial K+ (cell injury) and % LDH leakage (cell death) in non-induced (untreated) and phenobarbital-pretreated suspended hepatocytes. CCl4 and CHCl3 were delivered alone and in combination in dimethyl sulfoxide (DMSO) to suspended hepatocytes. The maximum observed no-effect level (MONEL) for CCl4 in non-induced cells was 1.0 mM (LDH and K+). In induced cells, the MONEL was 0.25 mM (K+) and 0.5 mM (LDH). The MONEL for CHCl3 in non-induced cells was 5.0 mM (LDH and K+) and in induced cells was 0.5 mM (K+) and 1.0 mM (LDH). Phenobarbital pretreatment enhanced the toxicity of both CCl4 and CHCl3, alone and in combination. RSM analysis of the % initial K+ and % LDH for CCl4 and CHCl3 in combination in noninduced and induced cells showed a greater than additive interaction. The isolated hepatocyte model appears to be a promising system for evaluating the toxicity of chemical mixtures and predicting their in vivo effects.
本研究的目的是评估一种分离的肝细胞模型,用于预测四氯化碳(CCl4)和氯仿(CHCl3)单独及联合使用时的体内肝毒性。采用响应面法(RSM)分析和描述数据。评估了未诱导(未处理)和苯巴比妥预处理的悬浮肝细胞中初始K+百分比(细胞损伤)和LDH泄漏百分比(细胞死亡)之间的相互作用。将CCl4和CHCl3单独及联合溶于二甲基亚砜(DMSO)后加入悬浮肝细胞中。未诱导细胞中CCl4的最大无效应水平(MONEL)为1.0 mM(LDH和K+)。在诱导细胞中,MONEL为0.25 mM(K+)和0.5 mM(LDH)。未诱导细胞中CHCl3的MONEL为5.0 mM(LDH和K+),诱导细胞中为0.5 mM(K+)和1.0 mM(LDH)。苯巴比妥预处理增强了CCl4和CHCl3单独及联合使用时的毒性。对未诱导和诱导细胞中CCl4和CHCl3联合使用时的初始K+百分比和LDH百分比进行RSM分析,结果显示存在大于相加的相互作用。分离的肝细胞模型似乎是一个很有前景的系统,可用于评估化学混合物的毒性并预测其体内效应。