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Vol. 288, Issue 1, 274-280, January 1999
Center for the Neurobiological Investigation of Drug Abuse,
Department of Physiology and Pharmacology, Bowman Gray School of
Medicine, Wake Forest University, Winston-Salem, North Carolina
The abuse of cocaine/opiate combinations (speedball) represents a
growing trend in illicit drug use. Delineation of neurobiological substrates mediating the reinforcing effects of the combination may
increase our knowledge of reinforcement mechanisms and provide useful
new information for the development of pharmacotherapies. Several
studies suggest dopaminergic innervations of the nucleus accumbens
(NAc) have a central role in the brain processes underlying drug
reinforcement. The present study was undertaken to determine the
relationship between the self-administration of cocaine/heroin combinations and NAc extracellular dopamine concentrations
([DA]e) using in vivo microdialysis and microbore
high-pressure liquid chromatography. Rats were assigned randomly
to one of three groups to self-administer i.v. cocaine (125, 250, and
500 µg/infusion; n = 5), heroin (4.5, 9, and 18 µg/infusion; n = 5), or cocaine/heroin combinations (125/4.5; 250/9, and 500/18 µg/infusion;
n = 4) under a fixed ratio (FR) 10: 20-s time-out
schedule of reinforcement/multicomponent dosing session. After stable
rates of responding were engendered and maintained, microdialysis
samples were collected in 10-min intervals during the
self-administration session. Self-administration of cocaine/heroin
combinations produced synergisitic elevations in NAc
[DA]e (1000% baseline) compared with cocaine (400%
baseline) and heroin (not significantly different from baseline
levels). Neither the number of infusions nor the interinfusion
intervals was significantly different between the groups across the
self-administration session. Moreover, cocaine concentrations were not
significantly different between the cocaine and cocaine/heroin groups.
These results demonstrate that heroin interacts with cocaine to produce synergistic elevations in [DA]e, providing a
neurochemical basis for understanding the abuse liability of
cocaine/opiate combinations.
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