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Vol. 283, Issue 3, 1375-1382, 1997
Department of Pharmacology and Therapeutics, University of
Liverpool, Liverpool L69 3BX, UK
Clozapine is associated with a 0.8% incidence of agranulocytosis.
Bioactivation to an unstable protein-reactive metabolite, identified as
a nitrenium intermediate, has been implicated in the toxicity. In this
study, we investigated whether the reactive metabolite is cytotoxic
toward polymorphonuclear leukocytes and mononuclear leukocytes using
horseradish peroxidase and H2O2 to generate the
metabolite in situ. In the absence of a full
metabolizing system (i.e., lack of horseradish peroxidase and/or
H2O2), clozapine (0-100 µM) and its stable
metabolites were not cytotoxic. With a full metabolizing system, both
clozapine (30 µM) and demethylclozapine exhibited cytotoxicity toward
polymorphonuclear leukocytes (50.7 ± 7.7% and 17.6 ± 1.2%
cell death, respectively) and mononuclear leukocytes (36.6 ± 2.1% and 24.6 ± 4.1%, respectively), whereas clozapine N-oxide
was not cytotoxic. Exogenous glutathione (GSH), N-acetylcysteine and
ascorbic acid all protected the cells. Bioactivation of clozapine and
demethylclozapine, but not the N-oxide, was accompanied by depletion of
intracellular GSH. [14C]Clozapine was metabolized to the
previously identified C6 and C9 glutathionyl conjugates; GSH conjugates
were also detected when demethylclozapine and clozapine N-oxide were
bioactivated by horseradish peroxidase and
H2O2. In conclusion, using a novel in
vitro assay, we have shown that clozapine and its stable
metabolites are not cytotoxic per se but are
bioactivated to cytotoxic metabolites. The cytotoxic metabolite of
clozapine is identical to the protein-reactive metabolite that has been
characterized previously. These cytotoxic metabolites may play an
important role in the pathogenesis of clozapine agranulocytosis; the
mechanism by which this occurs is currently being investigated.
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