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Vol. 282, Issue 2, 591-596, 1997
Department of Psychiatry, School of Medicine, University of
California, San Diego, La Jolla (R.K., D.S.S.) and Department of
Medicinal and Molecular Pharmacology, University of California, Los
Angeles, Health Sciences Center, Los Angeles, California
To further delineate amphetamine-dopamine
pharmacokinetic-pharmacodynamic relationships, we examined
extracellular levels of dopamine and amphetamine in caudate-putamen
after the s.c. administration of 8 mg/kg amphetamine. In a parallel
group of animals, we also assessed caudate-putamen tissue levels of the drug. Extracellular concentrations of the transmitter and the drug
exhibited similar temporal profiles, each achieving maximum concentrations within 30 min of drug administration. Tissue levels of
amphetamine exhibited a similar, although slightly earlier time to
maximum levels. The concentrations of amphetamine and dopamine in the
extracellular fluid and amphetamine in tissue rapidly declined with
similar rates of elimination. In contrast to the temporal profiles for
both dopamine and amphetamine, stereotyped behaviors achieved maximum
intensity at about 60 min. In addition, although transmitter and drug
declined almost 10-fold from maximum values over the 4-hr interval
after amphetamine administration, stereotyped behaviors persisted for
at least 3 hr before abating. The results of these studies confirm our
previous observation that the temporal profiles for stereotyped
behaviors and extracellular dopamine are dissociated, and also extend
this dissociation to extracellular amphetamine. In addition, although
there was a close correspondence between dopamine and amphetamine
within each experimental animal, individual animals exhibited a broad
range of maximal dopamine responses, suggesting a differential
responsiveness to amphetamine.