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Vol. 288, Issue 2, 699-709, February 1999
Department of Psychiatry, School of Medicine, University of
California, San Diego, La Jolla, California
The quantitative and qualitative features of the behavioral response to
amphetamine-like stimulants in rats can be dissociated from the
dopamine response. This dissociation is particularly evident in the
temporal profiles of the extracellular dopamine and stereotypy
responses to higher doses of amphetamine. One possible mechanism
contributing to this temporal dissociation is that during the acute
response to amphetamine, dopamine receptor mechanisms are enhanced such
that stereotyped behaviors can be supported by synaptic concentrations
of dopamine which are not sufficient to initiate these behaviors. To
further explore the dynamics of stimulant sensitivity during the acute
response, we examined the behavioral and extracellular dopamine
responses to a low, nonstereotypy-producing dose of amphetamine (0.5 mg/kg) at various times after an acute, priming injection of 4.0 mg/kg
when stereotypies had subsided and extracellular dopamine was
approaching predrug baseline levels. The low-dose challenge produced
intense stereotypies although the regional dopamine responses were not
significantly different from control animals. Blockade of the
expression of stereotypies during the priming response by the D2
antagonist haloperidol or the D1 antagonist SCH 23390 prevented the
expression of an enhanced stereotypy response to the challenge
injection. Our results suggest that an exposure to amphetamine results
in a rapid sensitization of the stereotypy response which does not
involve changes in the extracellular dopamine response but requires
activation of dopamine receptors. Such a mechanism may be significantly
implicated during binge patterns of stimulant abuse and may also play a
role in the sensitization associated with repeated amphetamine administration.
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