Cytochrome P450 2E1 (CYP2E1) is the principal enzyme responsible for urethane metabolism: comparative studies using CYP2E1-null and wild-type mice

摘要

Urethane ([carbonyl-~(14)C]ethyl carbamate) is a fermentation byproduct in alcoholic beverages and foods and is classified as reasonably anticipated to be a human carcinogen. Early studies indicates that while CYP2E1 is involved, esterases are the primary enzymes responsible for urethane metabolism. Using CYP2E1-null (KO) mice, current studies were undertaken to elucidate CYP2E1's contribution to urethane metabolism. [Carbonyl-~(14)C]urethane was administered by gavage to male CYP2E1-null and wild-type mice at 10 to 100 mg/kg and its metabolism and disposition were investigated. CO_2 was confirmed as the main metabolite of urethane. Significant inhibition of urethane metabolism to CO_2 occurred in CYP2E1-null versus wild-type mice. Pharmacokinetic modelling of ~(14)CO_2 exhalation data revealed that CYP2E1 is responsible for approximately 96% of urethane metabolism to CO_2 in wild-type mice. The contributions of other enzymes to urethane metabolism merely account for the remaining 4%. The half-life of urethane in wild-type and CYP2E1-null mice was estimated at 0.8 and 22 h, respectively. Additionally, the concentration of urethane-derived radioactivity in blood and tissues was dose-dependent and significantly ghier in CYP2E1-null mice. High-performance liquid chromatography analysis showed only urethane in the plasma and liver extracts of CYP2D1-null mice. Because the lack of CYP2E1did not completely inhibit urethane metabolism, the disposition of 10 mg/kg urethane was compared in mice pretreated with the P450 inhibitor, 1-aminobenzotriazole or the esterase inhibitor, paraoxon. Unlike paraoxon, 1-aminobenzotriazole resulted in significant inhibition of urethane mitabolism to CO_2 in both genotypes. In conclusion, this work demonstrated that CYP2E1, not esterase, is the principal enzyme responsible for urethane metabolism.