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Molecular Pharmacology, Vol 10, 225-234, Copyright © 1974 by the American Society for Pharmacology and Experimental Therapeutics
1 Laboratory of Preclinical Pharmacology, National Institute of Mental Health,
Saint Elizabeths Hospital, Washington, D. C. 20032
Dopamine in the rat corpus striatum declines biphasically after intraperitoneal injection
of 0.81 nmole/kg of
-methyl-p-tryosine methyl ester. This confirms the results of Javoy
and Glowinski [(1971) J. Neurochem., 18: 1305-1311]. The rapid initial decline in striatal
dopamine is coincident with p-hydroxyamphetamine and p-hydroxynorephedrine concentrations of 1.2 and 8.2 nmoles/g of brain, respectively. Similar concentrations are present in
the striatum. p-Hydroxyamphetamine and p-hydroxynorephedrine may be responsible for
the fast initial decline in striatal dopamine after treatment with
-methyl-p-tyrosine methyl
ester, because these compounds change the kinetics of striatal dopamine, presumably by
increasing its efflux. Moreover, the conversion index of striatal labeled tyrosine to striatal
dopamine is inhibited only 53% between 5 and 15 min after injection of
-methyl-p-tyrosine
methyl ester. We propose a new method for calculating the turnover rate of striatal dopamine, based on normalized plots of the change with time of the specific activity of striatal
tyrosine and dopamine after injection of tracer amounts of [3H]tyrosine. The transformation
constant (
) is defined by the fractional rate constant of tyrosine (kTyr) and is calculated
as equal to 1/kTyr. This kinetic analysis yields an estimate of the striatal dopamine turnover rate in agreement with values estimated by other methods. The experimental data are
incompatible with a two-compartment model of dopamine: a functional compartment (26%
of the store) and a main storage compartment (74% of the store) with k values of 4.6 and
0.34 hr-1, respectively, as proposed by Javoy and Glowinski. Calculations show that the
0.34 hr-1 rate for a single striatal dopamine compartment exceeds the limits imposed by
the change with time of striatal dopamine specific radioactivity after a tracer injection of
[3H]tyrosine.
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