TY - JOUR T1 - UDP-GLUCURONOSYLTRANSFERASE 2B7 IS THE MAJOR ENZYME RESPONSIBLE FOR GEMCABENE GLUCURONIDATION IN HUMAN LIVER MICROSOMES JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 1349 LP - 1354 DO - 10.1124/dmd.105.005108 VL - 33 IS - 9 AU - Jonathan N. Bauman AU - Theunis C. Goosen AU - Meera Tugnait AU - Vincent Peterkin AU - Susan I. Hurst AU - Lee C. Menning AU - Mark Milad AU - Michael H. Court AU - J. Andrew Williams Y1 - 2005/09/01 UR - http://dmd.aspetjournals.org/content/33/9/1349.abstract N2 - The predominant metabolic pathway of gemcabene in humans is glucuronidation. The principal human UDP-glucuronosyltransferases (UGTs) involved in the glucuronidation of gemcabene were determined in this study. Glucuronidation of gemcabene was catalyzed by recombinant UGT1A3, recombinant UGT2B7, and recombinant UGT2B17, as well as by human liver microsomes (HLM). Gemcabene glucuronidation in recombinant UGTs and HLM followed non-Michaelis-Menten kinetics consistent with homotropic activation, but pharmacokinetics in humans were linear over the dose range tested (total plasma Cmax, 0.06–0.88 mM). Gemcabene showed similar affinity (S50) for recombinant UGTs (0.92–1.45 mM) and HLM (1.37 mM). S-Flurbiprofen was identified as a more selective inhibitor of recombinant UGT2B7-catalyzed gemcabene glucuronidation (>23-fold lower IC50) when compared with recombinant UGT1A3- or recombinant UGT2B17-catalyzed gemcabene glucuronidation. The IC50 for S-flurbiprofen inhibition of gemcabene glucuronidation was similar in HLM (60.6 μM) compared with recombinant UGT2B7 (27.4 μM), consistent with a major role for UGT2B7 in gemcabene glucuronidation in HLM. In addition, 5,6,7,3′,4′,5′-hexamethoxyflavone inhibited recombinant UGT1A3 and recombinant UGT2B17-catalyzed gemcabene glucuronidation (with 4-fold greater potency for recombinant UGT1A3) but did not inhibit gemcabene glucuronidation in HLM, suggesting that UGT1A3 and UGT2B17 do not contribute significantly to gemcabene glucuronidation. Reaction rates for gemcabene glucuronidation from a human liver bank correlated well (r2 = 0.722, P < 0.0001; n = 24) with rates of glucuronidation of the UGT2B7 probe substrate 3′-azido-3′-deoxythymidine. In conclusion, using the three independent experimental approaches typically used for cytochrome P450 reaction phenotyping, UGT2B7 is the major enzyme contributing to gemcabene glucuronidation in human liver microsomes. The American Society for Pharmacology and Experimental Therapeutics ER -