J. Fang et al., In vitro characterization of the metabolism of haloperidol using recombinant cytochrome P450 enzymes and human liver microsomes, DRUG META D, 29(12), 2001, pp. 1638-1643
A systematic in vitro study was carried out to elucidate the enzymes respon
sible for the metabolism of haloperidol (HAL) using human liver microsomes
and recombinant human cytochrome P450 isoenzymes. In the first series of ex
periments, recombinant cytochrome P450 (P450) isoenzymes were used to evalu
ate their catalytic involvement in the metabolic pathways of HAL. Recombina
nt CYP3A4, CYP3A5, and CYP1A1 were shown to be able to catalyze the metabol
ism of HAL to its pyridinium analog (HP+) and the oxidation of reduced HAL
(RH) back to HAL; Recombinant CYP3A4, CYP3A5, CYP1A1, CYP2C19, CYP2C8, CYP2
C9, and CYP2D6 were able to catalyze the dealkylation of HAL to 4-(4-chloro
phenyl)-4-hydroxypiperidine (CPHP). CYP3A4 was capable of metabolizing HAL
to its tetrahydropyridine analog 4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4
-oxobutyl] -1,2,3,6-tetrahydropyridine and metabolizing to CPHP; CYP3A4 and
CYP3A5 were able to metabolize RH to its pyridinium analog (RHP); CYP1A1,
CYP1A2, and CYP3A4 were able to catalyze the oxidation of RHP+ to HP+. In t
he second series of experiments, the metabolic activities of human liver mi
crosomes from 12 donors were correlated with catalytic activities of select
ive substrates of different P450 isoenzymes and immuno-reactivities toward
different P450 isoenzymes. CYP3A4 activities were found to correlate to all
the seven metabolic pathways of HAL mentioned above. This suggests a promi
nent role for CYP3A4 in the metabolism of HAL. Interestingly, it was found
that recombinant CYP1A1 has the highest activity for oxidizing RHP+ to HP+.
The activity of recombinant CYP1A1 was 50 times higher than CYP1A2 and 220
times higher than CYP3A4.