TY - JOUR T1 - Drug Metabolizing Capacity of Cryopreserved Human, Rat, and Mouse Liver Parenchymal Cells in Suspension JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 1415 LP - 1422 VL - 27 IS - 12 AU - Pablo Steinberg AU - Thomas Fischer AU - Sandra Kiulies AU - Katja Biefang AU - Karl-Ludwig Platt AU - Franz Oesch AU - Thomas Böttger AU - Clemens Bulitta AU - Peter Kempf AU - Jan Hengstler Y1 - 1999/12/01 UR - http://dmd.aspetjournals.org/content/27/12/1415.abstract N2 - The phase I and phase II drug-metabolizing capacity of freshly isolated and cryopreserved parenchymal cells (PC) from human, rat, and mouse liver held in suspension at 37°C for up to 120 min after thawing was compared. Although 7-ethoxycoumarin-O-deethylase activity was strongly reduced in freshly isolated as well as in cryopreserved PC from human, rat, and mouse liver after 120 min, 7-ethoxyresorufin-O-deethylase activity as well as the profile and formation rates of hydroxylated testosterone metabolites in general remained constant throughout the 2-h incubation period in cryopreserved PC from all three species and was similar to that measured in freshly isolated PC. The activity of glutathioneS-transferase (GST) and that of UDP- glucuronosyltransferase (UDP-GT) toward 4-methylumbelliferone significantly decreased, whereas the activities of UDP-GT activity toward 4-hydroxybiphenyl and sulfotransferase in cryopreserved human PC were similar to those measured in freshly isolated PC. The activities of GST, UDP-GT toward 4-methylumbelliferone, and sulfotransferase in cryopreserved rat PC showed a significant decrease when compared with the activities in freshly isolated PC. The phase II enzyme activities in cryopreserved mouse PC proved to be far more stable, being similar to the activities of freshly isolated mouse PC at all four time points measured with the exception of GST, which showed a decay from t = 60 min onward. In conclusion, phase I drug-metabolizing enzyme activities in cryopreserved human, rat, and mouse PC are very similar to those of freshly isolated PC, whereas phase II enzyme activities are affected by cryopreservation. The American Society for Pharmacology and Experimental Therapeutics ER -