학술논문

The new designer drug buphedrone produces rewarding properties via dopamine D1 receptor activation.
Document Type
Journal Article
Source
Addiction Biology. Jan2018, Vol. 23 Issue 1, p69-79. 11p.
Subject
*REWARD (Psychology)
*DOPAMINE receptors
*CATHINONE
*DRUG-seeking behavior
*LABORATORY mice
*WESTERN immunoblotting
*AMINES
*ANIMAL experimentation
*BASAL ganglia
*BENZAMIDE
*CELL receptors
*COMPARATIVE studies
*CONDITIONED response
*DESIGNER drugs
*DOPAMINE antagonists
*HETEROCYCLIC compounds
*HUMAN locomotion
*KETONES
*RESEARCH methodology
*DOPAMINE uptake inhibitors
*MEDICAL cooperation
*METHAMPHETAMINE
*MICE
*PRIMATES
*RESEARCH
*SELF medication
*EVALUATION research
*PHARMACODYNAMICS
Language
ISSN
1355-6215
Abstract
Substituted cathinones are synthetic analogs of the active components of natural products and are widely abused worldwide. However, the rewarding properties of these agents have not yet been evaluated. In this study, we investigated the abuse potential of buphedrone [2-(methylamino)-1-phenylbutan-1-one, α-methylamino-butyrophenone] and its effects on the mesolimbic dopaminergic system in mice using conditioned place preference (CPP) analysis, a self-administration test, a locomotor activity test, a behavioral sensitization test and Western blot analysis. Treatment with buphedrone supported CPP and self-administration, enhanced locomotor activity and produced behavioral sensitization when mice were challenged with methamphetamine. SCH23390, a D1 dopamine antagonist, prevented buphedrone-induced CPP, whereas raclopride, a D2 dopamine antagonist, had no effect. SCH23390 also blocked locomotor activity increase by buphedrone, while raclopride partially attenuated locomotor activation. Western blot analysis revealed that repeated buphedrone treatment increased D1 dopamine receptor expression in the dorsal striatum and nucleus accumbens in mice. Collectively, these findings suggest the abuse potential of buphedrone and demonstrate the involvement of the dopaminergic system in the establishment of its rewarding properties. [ABSTRACT FROM AUTHOR]