A review of the effects of dopaminergic agents on humans, animals, and drug-seeking behavior, and its implications for medication development. Focus on GBR 12909
Rothman RB, Glowa JR
Clinical Psychopharmacology Section,
Baltimore, MD 21224, USA.
Mol Neurobiol 1995 Aug-Dec;11(1-3):1-19


Medication development for cocaine abuse has focused on potential mechanisms of action related to the abuse of cocaine. The hypothesis that mesolimbic dopamine (DA) is the key neurochemical mediator of cocaine's addictive and reinforcing effects is well supported by a wide variety of data from animal studies. On the other hand, medications that increase DA or block its action in humans can produce effects that appear incompatible with this hypothesis. This article reviews these incompatibilities between animal and human data with a focus on the DAergic actions of drugs, including DA reuptake inhibitors, direct DA agonists, DA increasers, and DA antagonists. Possible reasons for these discrepancies are discussed, and the potential role of high-affinity DA uptake inhibitors, such as GBR12909, for pharmacotherapies for treating cocaine addiction in humans is likely to come from understanding its mechanisms of action, it is clear that further research on the effects of cocaine in humans and animals will be critical to the medication development effort.

Cocaine hotspots
Dopaminergic flies?
Coca leaves/cocaine
Cocaine immunization
The coke-craving brain
Vanoxerine (GBR 12909) : structure
GBR12909: a dopaminergic antidepressant?

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