CYTOCHROME-P450 ENZYMES INVOLVED IN ACETAMINOPHEN ACTIVATION BY RAT AND HUMAN LIVER-MICROSOMES AND THEIR KINETICS

Acetaminophen (APAP), a commonly used analgesic, is catalyzed by cytoc hrome P450 (P450) enzymes to a toxic intermediate which can be trapped by glutathione. Using this approach, involvement of enzymes in the ac tivation of APAP and their kinetics were studied. With human liver mic rosomes, there were three apparent K(m) values (approximately 10, 474, and 13 000 AM) for the oxidation of APAP to its glutathione conjugate . With rat liver microsomes (control and ethanol induced) the kinetic data were best fit to a two-Km model (approximately 30 and 1100 muM). Liver microsomes from dexamethasone (DEX)-treated female rats showed a single K(m) of 56 muM and a V(max) of 7500 pmol of product formed/ (m in-mg of protein). Antibodies specific for rat P450s 2E1 and 1A2 each inhibited approximately 40% of the APAP metabolism in control male rat microsomes. Only slight inhibition was observed with the P450 3A1/2 a ntibodies in control male or female rat liver microsomes. Antibodies a gainst rat P450s 3A1/2 inhibited the activity in DEX microsomes by 80 %. Antibodies inhibitory to human P450 3A4 inhibited 38% of the activi ty in human liver microsome sample HL107 and 76% in human microsome sa mple HL110. Human P450s (2A6, 2E1, 1A2, 3A4, 3A5, 3A3, 2D6, 2F1, 2C8, 2B6, and 2C9) expressed in Hep G2 cells using a vaccinia virus express ion system were each tested for APAP metabolism. Of these, P450 2E1, 1 A2, and 3A4 showed substantial activity, with respective K(m) and V(ma x) values of 680 muM and 330 pmol/(min-mg) for P450 2E1 (with added cy tochrome b5), 3430 muM and 74 pmol/(min.mg) for P450 1A2, and 280 muM and 130 pmol/(min.mg) for P450 3A4. In the presence of alpha-naphthofl avone (alpha-NF), expressed P450 3A4 activity was increased 11-fold, e xpressed P450 2E1 activity was unaffected, and expressed 1A2 activity was inhibited 83%. With expressed P450 3A4, both the K(m) and V(max) f or APAP oxidation were increased by alpha-NF. Alpha-NF stimulated APAP oxidation 2- to 5-fold in human and control male rat liver microsomes . In the presence of alpha-NF, the P450 3A1/2 antibody became strongly inhibitory in control male rat liver microsomes, suggesting 3A2 activ ation by this flavone compound.