Journal
DRUG METABOLISM AND DISPOSITION
Volume 34, Issue 9, Pages 1606-1614Publisher
AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/dmd.106.010439
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Cytochromes P450 ( P450s) are major catalysts in the metabolism of xenobiotics and endogenous substrates such as estradiol (E-2). It has previously been shown that E2 is predominantly metabolized in humans by CYP1A2 and CYP3A4 with 2-hydroxyestradiol (2-OHE2) the major metabolite. This study examines effects of deployment-related and other chemicals on E2 metabolism by human liver microsomes ( HLM) and individual P450 isoforms. Kinetic studies using HLM, CYP3A4, and CYP1A2 showed similar affinities ( Km) for E2 with respect to 2-OHE2 production. V-max and CLint values for HLM are 0.32 nmol/min/mg protein and 7.5 mu l/min/mg protein; those for CYP3A4 are 6.9 nmol/min/nmol P450 and 291 mu l/min/ nmol P450; and those for CYP1A2 are 17.4 nmol/min/nmol P450 and 633 mu l/min/nmol P450. Phenotyped HLM use showed that individuals with high levels of CYP1A2 and CYP3A4 have the greatest potential to metabolize E-2. Preincubation of HLM with a variety of chemicals, including those used in military deployments, resulted in varying levels of inhibition of E-2 metabolism. The greatest inhibition was observed with organophosphorus compounds, including chlorpyrifos and fonofos, with up to 80% inhibition for 2-OHE2 production. Carbaryl, a carbamate pesticide, and naphthalene, a jet fuel component, inhibited ca. 40% of E-2 metabolism. Preincubation of CYP1A2 with chlorpyrifos, fonofos, carbaryl, or naphthalene resulted in 96, 59, 84, and 87% inhibition of E-2 metabolism, respectively. Preincubation of CYP3A4 with chlorpyrifos, fonofos, deltamethrin, or permethrin resulted in 94, 87, 58, and 37% inhibition of E-2 metabolism. Chlorpyrifos inhibition of E-2 metabolism is shown to be irreversible.
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