PT  - JOURNAL ARTICLE
AU  - Deepak Dalvie
AU  - Chenghong Zhang
AU  - Weichao Chen
AU  - Teresa Smolarek
AU  - R. Scott Obach
AU  - Cho-Ming Loi
TI  - Cross-Species Comparison of the Metabolism and Excretion of Zoniporide: Contribution of Aldehyde Oxidase to Interspecies Differences
AID  - 10.1124/dmd.109.030783
DP  - 2010 Apr 01
TA  - Drug Metabolism and Disposition
PG  - 641--654
VI  - 38
IP  - 4
4099  - http://dmd.aspetjournals.org/content/38/4/641.short
4100  - http://dmd.aspetjournals.org/content/38/4/641.full
SO  - Drug Metab Dispos2010 Apr 01; 38
AB  - Excretion and metabolism of zoniporide were investigated in humans after intravenous infusion of [14C]zoniporide at an 80-mg dose. Bile was the primary route of excretion because 57% of dose was recovered in the feces after intravenous infusion. Zoniporide was primarily cleared via metabolism in humans. 2-Oxozoniporide (M1) was the major excretory and circulating metabolite in humans and was catalyzed by aldehyde oxidase (Km of 3.4 μM and Vmax of 74 pmol/min/mg protein). Metabolites M2 (17% of the dose) and M3 (6.4% of circulating radioactivity), in which the guanidine moiety was hydrolyzed to a carboxylic acid, were also detected in human feces and plasma, respectively, suggesting that hydrolysis was another route of metabolism of zoniporide in humans. The metabolism and excretion of [14C]zoniporide in rats and dogs were also evaluated. As in humans, bile was the primary route of excretion of the radiolabeled material in both species, and metabolism was the primary route of clearance. A comparison of plasma metabolites showed that for M3, rats had a higher concentration than human or dog. M1 was absent in dog and present in human and rat plasma at comparable levels, whereas comparison of excreta showed that the total body burden of M1 was greater in rat than that in human. No further evaluation of M2 was considered because it was detected only in the human fecal extracts. Hence, no further toxicological evaluation of the three human metabolites was undertaken. Copyright © 2010 by The American Society for Pharmacology and Experimental Therapeutics