Cd. Davis et al., KINETIC-PARAMETERS OF LYMPHOCYTE MICROSOMAL EPOXIDE HYDROLASE IN CARBAMAZEPINE HYPERSENSITIVE PATIENTS - ASSESSMENT BY RADIOMETRIC HPLC, Biochemical pharmacology, 50(9), 1995, pp. 1361-1366
Idiosyncratic hypersensitivity reactions with carbamazepine have been
postulated to be due to a deficiency of microsomal epoxide hydrolase (
HYL1), although this is based on indirect evidence. Using H-3-cis stil
bene oxide (0.5 Gi/mmol) as a substrate, we have developed a radiometr
ic HPLC assay sensitive enough to measure the kinetic parameters of HY
L1 in lymphocytes. The intra-assay coefficient of variation was 8%. En
zyme activity has been measured in lymphocytes from six carbamazepine
hypersensitive patients, six patients on carbamazepine without any adv
erse effects, and twelve drug-naive healthy volunteers. No significant
difference was observed in three kinetic parameters of the enzyme amo
ng these three groups. The values for K-m, V-max, and intrinsic cleara
nce ranged from 6.1-89.9 mu M, 3.0-23.2 pmoles diol formed/min/mg prot
ein, and 0.147-0.493 mu l/min/mg protein. There was no difference in e
nzyme activity between patients currently on carbamazepine and healthy
volunteers, indicating a lack of induction of lymphocyte HYL1 by carb
amazepine. Go-incubation of lymphocytes with 1,1,1-trichloropropene ox
ide, an inhibitor of hepatic HYL1, resulted in an 82% inhibition of ac
tivity, similar to that observed with the hepatic enzyme. The healthy
volunteers were genotyped as being either GSTM1 positive (n = 6) or GS
TM1 negative (n = 6). This did not affect the kinetic parameters of ly
mphocyte microsomal epoxide hydrolase. Our results suggest that there
is normal HYL1 activity in lymphocytes of hypersensitive patients usin
g cis-stilbene oxide as a substrate.