Götz R, Schwarz L R, Greim H
Arch Toxicol. 1980 Mar;44(1-3):147-55. doi: 10.1007/BF00303191.
The effect of pentachlorophenol (PCP) and 2,4,6-tricholorphenol (2,4,6-T) on the disposition of the hepatodiagnostic dye, sulfobromophthalein (BSP) has been studied in isolated liver cells. PCP (4-6 microM) as well as 2,4,6-T (50-100 microM) interferes with the disposition of BSP. The main effect apparently occurs at the secretion step as both drugs severely impair the release of the glutathione conjugate of BSP into the medium. As a consequence, BSP and its conjugate accumulate in the cell. High doses of PCP did not increase the release of lactate dehydrogenase from the hepatocytes. Concentrations of the two phenols which interfere with the secretion of BSP also completely uncouple the oxidative phosphorylation of hepatocellular mitochondria. The dysfunction of liver cells described here may therefore be explained by the effect of PCP and 2,4,6-T on the energy production of the cells. The higher toxicity of PCP as compared to 2,4,6-T observed in our system corresponds well with the higher LD50 of the latter compound.
在离体肝细胞中研究了五氯苯酚(PCP)和2,4,6 - 三氯苯酚(2,4,6 - T)对肝脏诊断染料磺溴酞钠(BSP)代谢的影响。PCP(4 - 6微摩尔)以及2,4,6 - T(50 - 100微摩尔)会干扰BSP的代谢。主要影响显然发生在分泌步骤,因为这两种药物都会严重损害BSP的谷胱甘肽共轭物释放到培养基中。结果,BSP及其共轭物在细胞内积累。高剂量的PCP不会增加肝细胞中乳酸脱氢酶的释放。干扰BSP分泌的两种酚类物质的浓度也会完全解偶联肝细胞线粒体的氧化磷酸化。因此,这里描述的肝细胞功能障碍可能是由PCP和2,4,6 - T对细胞能量产生的影响来解释的。在我们的系统中观察到PCP比2,4,6 - T具有更高的毒性,这与后一种化合物较高的半数致死剂量(LD50)相吻合。