PT  - JOURNAL ARTICLE
AU  - Yuji Mano
AU  - Takashi Usui
AU  - Hidetaka Kamimura
TI  - Comparison of Inhibition Potentials of Drugs against Zidovudine Glucuronidation in Rat Hepatocytes and Liver Microsomes
AID  - 10.1124/dmd.106.014225
DP  - 2007 Apr 01
TA  - Drug Metabolism and Disposition
PG  - 602--606
VI  - 35
IP  - 4
4099  - http://dmd.aspetjournals.org/content/35/4/602.short
4100  - http://dmd.aspetjournals.org/content/35/4/602.full
SO  - Drug Metab Dispos2007 Apr 01; 35
AB  - Hepatocytes and liver microsomes are considered to be useful for investigating drug metabolism catalyzed mainly via glucuronidation. However, there have been few reports comparing the glucuronidation inhibition potentials of drug in hepatocytes to those in liver microsomes. 3′-Azido-3′-deoxythymidine (AZT, zidovudine) glucuronidation (AZTG) is the major metabolic pathway for AZT. In this study, the inhibition potentials of drugs against UDP-glucuronosyltransferase (UGT)-catalyzed AZTG in the hepatocytes and liver microsomes of rats are compared. The AZTG inhibition potentials of diclofenac, diflunisal, fluconazole, indomethacin, ketoprofen, mefenamic acid, naproxen, niflumic acid, and valproic acid in liver microsomes and hepatocytes were investigated using liquid chromatography with tandem mass spectrometry. Diflunisal (inhibition type: noncompetitive) inhibited AZTG most potently in rat liver microsomes (RLMs) with an IC50 value of 34 μM. The IC50 values of diclofenac, fluconazole, indomethacin, ketoprofen, mefenamic acid, naproxen, niflumic acid, and valproic acid against AZTG in RLMs ranged from 34 to 1791 μM. Diclofenac, diflunisal, indomethacin, ketoprofen, naproxen, and valproic acid inhibited AZTG in hepatocytes with IC50 values of 58, 37, 88, 361, 486, and 281 μM, respectively. These values were similar to those obtained in RLMs. In conclusion, the AZT glucuronidation inhibition potentials of drugs in the hepatocytes and liver microsomes of rats were found to be similar, and liver microsomes can be useful for evaluating UGT isozyme inhibition potentials. The American Society for Pharmacology and Experimental Therapeutics