Regulation of extracellular dopamine
by the norepinephrine transporter
by
Yamamoto BK, Novotney S
Department of Psychiatry,
Case Western Reserve University
School of Medicine,
Cleveland, Ohio, USA.
J Neurochem 1998 Jul; 71(1):274-80
ABSTRACT
There is growing evidence of an interaction between dopamine and
norepinephrine. To test the hypothesis that norepinephrine terminals are
involved in the uptake and removal of dopamine from the extracellular space, the
norepinephrine uptake blocker desmethylimipramine (DMI) was infused locally
while the extracellular concentrations of dopamine were simultaneously
monitored. DMI increased the extracellular concentrations of dopamine in the
medial prefrontal cortex and nucleus accumbens shell but had no effect in the
striatum. The combined systemic administration of haloperidol and the local
infusion of DMI produced an augmented increase in extracellular dopamine in the
cortex compared with the increase produced by either drug alone. This
synergistic increase in dopamine overflow is likely due to the combination of
impulse-mediated dopamine release produced by haloperidol and blockade of the
norepinephrine transporter. No such synergistic effects were observed in the
nucleus accumbens and striatum. Local perfusion of the alpha2-antagonist
idazoxan also increased the extracellular concentrations of dopamine in the
cortex. Although the stimulation of extracellular dopamine by idazoxan and DMI
could be due to the increased extracellular concentrations of norepinephrine
produced by these drugs, an increase in dopamine also was observed in lesioned
rats that were depleted of norepinephrine and challenged with haloperidol. This
contrasted with the lack of an effect of haloperidol on cortical dopamine in
unlesioned controls. These results suggest that norepinephrine terminals
regulate extracellular dopamine concentrations in the medial prefrontal cortex
and to a lesser extent in the nucleus accumbens shell through the uptake of
dopamine by the norepinephrine transporter.
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