Evaluation of the xenobiotic biotransformation capability of six rodent hepatoma cell lines in comparison with rat hepatocytes

Phase I and II activities were examined in six rodent hepatoma cell lines and compared with those of cultured rat hepatocytes both in basal conditions and after exposure to 5µM methylcholanthrene, 2 mM phenobarbital, and 15µMβ-naphtoflavone. The metabolic profile of testosterone was also studied. The highest aryl hydrocarbon hydroxylase and 7-ethoxycoumarinO-deethylase activities were found in MH1C1 cells. Comparable values for 7-ethoxyresorufinO-deethylase activity, ranging from 21.6 to 42.9 pmol/mg × min, were observed in the hepatocytes and hepatoma cells, except the HTC cells. In contrast, only Fao cells showed 7-pentoxyresorufinO-depentylase activity at levels similar to those of hepatocytes (6.2±1.0 and 7.4±1.2 pmol/mg × min, respectively). Rat hepatocytes actively hydroxylatedp-nitrophenol, but this activity was not measurable in hepatoma cells. Glutathione transferase activity was maintained in all the hepatoma cell lines at similar levels to those found in hepatocytes (684 ± 56 nmol/mg × min). The seven hydroxylated metabolites of testosterone produced by cultured hepatocytes were negligible in hepatoma cells. Exposure of cells to inducers revealed that aryl hydrocarbon hydroxylase activity was mainly increased after treatment with 3-methylcholanthrene andβ-naphtoflavone, and the highest values were found in rat hepatocytes followed by MH1C1 and Fao cells. 3-Methylcholanthrene and naphtoflavone treatment also resulted in a marked increase in 7-ethoxyresorufinO-deethylase activity in hepatocytes as well as in H4IIC3, McA-Rh7777, MH1C1, and Fao cells. An enhancement of 7-ethoxycoumarinO-deethylase activity due to the three inducers was observed in both rat hepatocytes and hepatoma cells, with MH1C1 cells treated with methylcholanthrene showing the highest activity (727±74 pmol/mg × min). Increases in 7-pentoxyresorufinO-depentylase activity were detected after phenobarbital treatment of hepatocytes, MH1C1, and Fao cells, whereas a low response was observed in the other hepatoma cells. Of the six hepatoma cell lines examined, MH1C1 and Fao cells are the ones that are most similar to cultured rat hepatocytes in their expression of biotransformation activities.