We have studied striatal dopamine (DA) metabolism in monoamine oxidase (MAO
) B-deficient mice using brain microdialysis. Baseline DA levels were simil
ar in wild-type and knock-out (KO) mice. Administration of a selective MAO
A inhibitor, clorgyline (2 mg/kg), increased DA levels and decreased levels
of its metabolites in all mice, but a selective MAO B inhibitor, I-depreny
l (1 mg/kg), had no effect. Administration of 10 and 50 mg/kg L-DOPA, the p
recursor of DA, increased the levels of DA similarly in wild-type and KO mi
ce. The highest dose of L-DOPA (100 mg/kg) produced a larger increase in DA
in KO than wild-type mice. This difference was abolished by pretreating wi
ld-type mice with /-deprenyl. These results suggest that in mice, DA is onl
y metabolized by MAO A under basal conditions and by both MAO A and B at hi
gh concentrations. This is in contrast to the rat, where DA is always metab
olized by MAO A regardless of concentration.