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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on December 5, 2005; DOI: 10.1124/jpet.105.094045


0022-3565/06/3171-196-201$20.00
JPET 317:196-201, 2006
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NEUROPHARMACOLOGY

Differential Effects of Cocaine on Firing Rate and Pattern of Dopamine Neurons: Role of {alpha}1 Receptors and Comparison with L-Dopa and Apomorphine

Yan Zhou, Bejamin S. Bunney, and Wei-Xing Shi

Neuropsychopharmacological Research Unit, Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut

Psychostimulants, including cocaine, have two opposing effects on dopamine (DA) neurons: a DA-mediated inhibition and a non-DA-mediated excitation. The latter, expressed as an increase in both firing rate and a slow oscillation (SO) in firing pattern, has been shown to require forebrain inputs to DA neurons and activation of adrenergic {alpha}1 receptors. However, since the effect was observed when the DA-mediated inhibition was blocked by a D2 antagonist, it is uncertain whether the underlying mechanism also plays a role in cocaine's effects in normal animals where D2-like receptors are not blocked. This study showed that under such conditions, cocaine decreased firing rate and bursting without significantly inhibiting the SO in DA neurons recorded in the ventral tegmental area. Different from cocaine, L-dopa and apomorphine, two nonpsychostimulant DA agonists known to lack the {alpha}1-mediated excitatory effect, consistently inhibited all three measures of DA cell activity. Blockade of {alpha}1 receptors by prazosin did not enhance cocaine's ability to inhibit firing rate and bursting, but it did enable cocaine to inhibit the SO. These results suggest that in control rats where D2-like receptors are not blocked, {alpha}1 receptors play an important role in cocaine's effect on the SO but not in its effect on firing rate and bursting of DA neurons. The maintained SO after cocaine injection may reflect continued modulation of DA neurons by forebrain inputs, regulate the pattern of DA release, and provide a temporal structure for selection of synaptic inputs to DA neurons.


Received for publication August 9, 2005
Accepted December 2, 2005.

Address correspondence to: Dr. Wei-Xing Shi, Neuropsychopharmacological Research Unit, Yale University School of Medicine, 300 George Street, Room 8300C, New Haven, CT 06511. E-mail: wei-xing.shi{at}yale.edu




This article has been cited by other articles:


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M. Gao, C.-L. Liu, S. Yang, G.-Z. Jin, B. S. Bunney, and W.-X. Shi
Functional Coupling between the Prefrontal Cortex and Dopamine Neurons in the Ventral Tegmental Area
J. Neurosci., May 16, 2007; 27(20): 5414 - 5421.
[Abstract] [Full Text] [PDF]




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