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Research ArticleBehavioral Pharmacology

Dopamine β-Hydroxylase Inhibitors Enhance the Discriminative Stimulus Effects of Cocaine in Rats

Daniel F. Manvich, Lauren M. DePoy and David Weinshenker
Journal of Pharmacology and Experimental Therapeutics December 2013, 347 (3) 564-573; DOI: https://doi.org/10.1124/jpet.113.207746
Daniel F. Manvich
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia (D.F.M., D.W.); and Graduate Program in Neuroscience, Emory University, Atlanta, Georgia (L.M.D.)
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Lauren M. DePoy
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia (D.F.M., D.W.); and Graduate Program in Neuroscience, Emory University, Atlanta, Georgia (L.M.D.)
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David Weinshenker
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia (D.F.M., D.W.); and Graduate Program in Neuroscience, Emory University, Atlanta, Georgia (L.M.D.)
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Abstract

Inhibitors of dopamine β-hydroxylase (DBH), the enzyme that converts dopamine (DA) to norepinephrine (NE) in noradrenergic cells, have shown promise for the treatment of cocaine abuse disorders. However, the mechanisms underlying the beneficial effects of these compounds have not been fully elucidated. We used the drug discrimination paradigm to determine the impact of DBH inhibitors on the interoceptive stimulus properties of cocaine. Sprague-Dawley rats were trained to discriminate cocaine (5.6 mg/kg) from saline using a multicomponent, food-reinforced discrimination procedure. On test days, subjects were pretreated with the nonselective DBH inhibitor disulfiram (0–100.0 mg/kg i.p.) or the selective DBH inhibitor nepicastat (0–56.0 mg/kg i.p.) 2 hours prior to a test session either alone or in combination with cumulatively administered cocaine (0–5.6 mg/kg i.p.). Neither disulfiram nor nepicastat substituted for the cocaine stimulus when tested up to doses that nonspecifically reduced responding. However, in combination studies, pretreatment with either disulfiram or nepicastat produced leftward shifts in the cocaine dose-response function and also conferred cocaine-like stimulus effects to the selective NE transporter inhibitor, reboxetine (0.3–5.6 mg/kg i.p.). These results indicate that pharmacological inhibition of DBH does not produce cocaine-like interoceptive stimulus effects alone, but functionally enhances the interoceptive stimulus effects of cocaine, possibly due to facilitated increases in DA released from noradrenergic terminals. These findings suggest that DBH inhibitors have low abuse liability and provide support to clinical reports that some subjective effects produced by cocaine, particularly aversive effects, are enhanced after DBH inhibition.

Footnotes

    • Received July 5, 2013.
    • Accepted September 25, 2013.
  • This research was funded by the National Institutes of Health National Institute on Drug Abuse [Grants DA015040 and DA027535].

  • This work was previously presented at the following workshop: Manvich DF, DeBrouse L, and Weinshenker D (2013) Modulation of the discriminative-stimulus effects of cocaine by dopamine beta-hydroxylase inhibitors in rats. American Society for Pharmacology and Experimental Therapeutics; 2013 Apr 20–24; Boston, MA.

  • dx.doi.org/10.1124/jpet.113.207746.

  • Copyright © 2013 by The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 347 (3)
Journal of Pharmacology and Experimental Therapeutics
Vol. 347, Issue 3
1 Dec 2013
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Research ArticleBehavioral Pharmacology

DBH Inhibition and Cocaine Discrimination in Rats

Daniel F. Manvich, Lauren M. DePoy and David Weinshenker
Journal of Pharmacology and Experimental Therapeutics December 1, 2013, 347 (3) 564-573; DOI: https://doi.org/10.1124/jpet.113.207746

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Research ArticleBehavioral Pharmacology

DBH Inhibition and Cocaine Discrimination in Rats

Daniel F. Manvich, Lauren M. DePoy and David Weinshenker
Journal of Pharmacology and Experimental Therapeutics December 1, 2013, 347 (3) 564-573; DOI: https://doi.org/10.1124/jpet.113.207746
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