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PRECLINICAL STUDY: Difference in magnitude of psychostimulant‐induced extracellular norepinephrine in the ventral tegmental area contributes to discrepant prefrontal dopamine outflow
Author(s) -
Pan Wynn H. T.,
Hsieh MinChien,
Wu HsiaoHua,
Lin ShiKwang
Publication year - 2007
Publication title -
addiction biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.445
H-Index - 78
eISSN - 1369-1600
pISSN - 1355-6215
DOI - 10.1111/j.1369-1600.2006.00044.x
Subject(s) - ventral tegmental area , dopamine , extracellular , prefrontal cortex , amphetamine , chemistry , neuroscience , norepinephrine , medicine , endocrinology , pharmacology , dopaminergic , psychology , biochemistry , cognition
The dopamine (DA) efflux in the medial prefrontal cortex (mPFC) can be modulated by the interaction between afferent norepinephrine (NE) and somatodendritic DA in the ventral tegmental area (VTA). However, it is unclear how locally administered amphetamine (AMPH) or cocaine in the VTA results in discrepant response of DA efflux in the mPFC. In this study, intra‐VTA infusion of AMPH (1000 µM) or cocaine (200 µM) in anesthetized rats was employed to study the concurrent profile of extracellular DA level in the VTA and mPFC. In addition, the extracellular NE levels during the intra‐VTA infusion of these two psychostimulants were analyzed to compare their effects on prefrontal DA efflux. During the intra‐VTA infusion of AMPH, both extracellular DA and NE increased significantly in the VTA (270 ± 12% and 819 ± 40%, respectively). Meanwhile, the DA efflux in the mPFC elevated significantly. During the intra‐VTA infusion of cocaine, the extracellular DA and NE in the VTA also increased (271 ± 21% and 150 ± 15%, respectively). However, the DA efflux decreased significantly in the mPFC. Noteworthy, the increase of extracellular NE in the VTA was much more robust via AMPH infusion, as compared with cocaine. It is suggested that AMPH and cocaine enhance the extracellular NE concentrations in the VTA in different magnitudes, which in turn contribute to discrepant profiles of distal DA efflux in the mPFC.