N-glucuronidation reactions. I. Tetrazole N-glucuronidation of selected angiotensin II receptor antagonists in hepatic microsomes from rats, dogs, monkeys, and humans
Huskey, S.E.; Miller, R.R.; Chiu, S.H.
Drug Metabolism and Disposition the Biological Fate of Chemicals 21(5): 792-799
1993
ISSN/ISBN: 0090-9556 PMID: 7902238 Document Number: 419242
In vitro conditions for the preparation of tetrazole N2-glucuronides using liver microsomes (enriched with UDP-glucuronic acid) from rats, dogs, monkeys, and humans have been developed and optimized. The structures of tetrazole N2-glucuronides of 3 biphenyl tetrazole-containing angiotensin 11 (All) receptor antagonists MK-954 (1), L-158,338 (11), and L-158,809 (III), and a model compound methyl biphenyl tetrazole (IV) were determined either by NMR and mass spectrometry or by comparison of HPLC retention times with that from authentic compounds. The species difference as well as gender difference in the rate of the in vitro reaction were compared. The optimal pH for the reaction was determined to be 5.0 with liver microsomes from monkeys and humans, and 6.2 with those from rats and dogs. For the model compound IV, the rate of N2-glucuronidation by liver microsomes from rats, dogs, and monkeys was apprx 10-fold faster than that by humans. For the AII receptor antagonists I, II, and III, the rate of the same reaction by liver microsomes from dogs and monkeys was much faster then that by humans. The relative intrinsic rate of this reaction for these three substrates ranked similarly in rats and humans as II gt III gt I. With compound I, a biphenyl tetrazole-containing imidazole derivative that has potential sites for both O- (primary hydroxyl) and N2-(tetrazole) glucuronidation, both O- and tetrazole N2-glucuronides were formed by liver microsomes from rats and monkeys (at neutral pH), whereas N2-glucuronide was the only product from dogs and humans. These results were consistent with those previously reported for liver slices, and strongly suggest that different enzymes may be responsible for O- and tetrazole N2-glucuronidation. The rate of N2-glucuronidation was increased 2- to 3-fold when compound I was incubated with liver microsomes from female rats induced by phenobarbital or male rats by dexamethasone.