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Single‐dose disulfiram does not inhibit CYP2A6 activity
Author(s) -
Kharasch Evan D.,
Hankins Douglas C.,
Baxter Pamela J.,
Thummel Kenneth E.
Publication year - 1998
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1016/s0009-9236(98)90020-0
Subject(s) - disulfiram , cyp2a6 , pharmacology , cmax , chemistry , in vivo , pharmacokinetics , cyp2e1 , metabolite , excretion , coumarin , active metabolite , oral administration , drug interaction , medicine , biochemistry , metabolism , cytochrome p450 , cyp3a4 , biology , microbiology and biotechnology , organic chemistry
Background Disulfiram and its primary metabolite diethyldithiocarbamate are effective mechanism‐based inhibitors of human liver cytochrome P450 2E1 (CYP2E1) in vitro. A single dose of disulfiram, which significantly diminishes human P450 2E1 activity in vivo, has been used to investigate the role of CYP2E1 in human drug metabolism and to prevent CYP2E1‐mediated biotransformation. Nevertheless, the specificity of single‐dose disulfiram toward human CYP2E1 in vivo is unknown. Because diethyldithiocarbamate also inhibits human liver CYP2A6 in vitro, this investigation explored the effect of single‐dose disulfiram on human CYP2A6 activity in vivo. Methods CYP2A6 activity was assessed by the 7‐hydroxylation of coumarin, which is catalyzed selectively by CYP2A6. Ten healthy volunteers received 50 mg oral coumarin on two occasions in a randomized crossover design, approximately 10 hours after 500 mg oral disulfiram was administered or after no pretreatment (control group). Plasma and urine 7‐hydroxycoumarin and plasma coumarin concentrations were determined by HPLC. Results The area under the plasma 7‐hydroxycoumarin versus time curve (2.69 ± 0.90 μg · hr/ml) was not decreased after disulfiram pretreatment (3.33 ± 0.93 μg · hr/ml). Furthermore, maximum plasma concentration (C max ) of 7‐hydroxycoumarin (1.4 ± 0.5 versus 1.8 ± 0.6 μg/ml) and time to reach C max (1.0 ± 0.2 and 1.0 ± 0.4 hour) were unchanged by disulfiram pretreatment. Urinary 7‐hydroxycoumarin excretion over a 24‐hour period (38.9 ± 10.8 mg) was also undiminished by disulfiram pretreatment (45.2 ± 6.6 mg). Conclusions Single‐dose disulfiram does not inhibit human CYP2A6 activity in vivo. When single‐dose disulfiram is used as an in vivo probe for P450, inhibition of drug metabolism suggests involvement of CYP2E1 but not CYP2A6. Clinical Pharmacology & Therapeutics (1998) 64 , 39–45; doi: