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Research ArticleBEHAVIORAL PHARMACOLOGY

Monoaminergic Psychomotor Stimulants: Discriminative Stimulus Effects and Dopamine Efflux

Rajeev I. Desai, Carol A. Paronis, Jared Martin, Ramya Desai and Jack Bergman
Journal of Pharmacology and Experimental Therapeutics June 2010, 333 (3) 834-843; DOI: https://doi.org/10.1124/jpet.110.165746
Rajeev I. Desai
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Carol A. Paronis
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Jared Martin
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Ramya Desai
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Jack Bergman
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Abstract

The present studies were conducted to investigate the relationship between discriminative stimulus effects of indirectly acting monoaminergic psychostimulants and their ability to increase extracellular levels of dopamine (DA) in the nucleus accumbens (NAcb) shell. First, the behavioral effects of methamphetamine (MA), cocaine (COC), 1-[2-[bis(4-fluorophenyl-)methoxy]ethyl]-4-(3-phenylpropyl)piperazine (GBR 12909), d-amphetamine, and methylphenidate were established in rats trained to discriminate intraperitoneal injections of 0.3 mg/kg MA from saline. In other studies, in vivo microdialysis was used to determine the effects of MA, COC, and GBR 12909 on extracellular DA levels in the NAcb shell. Results show that all drugs produced dose-related and full substitution for the discriminative stimulus effects of 0.3 mg/kg MA. In microdialysis studies, cumulatively administered MA (0.3–3 mg/kg), COC (3–56 mg/kg), and GBR 12909 (3–30 mg/kg) produced dose-dependent increases in DA efflux in the NAcb shell to maxima of approximately 1200 to 1300% of control values. The increase in DA levels produced by MA and COC was rapid and short-lived, whereas the effect of GBR 12909 was slower and longer lasting. Dose-related increases in MA lever selection produced by MA, COC, and GBR 12909 corresponded with graded increases in DA levels in the NAcb shell. Doses of MA, COC, and GBR 12909 that produced full substitution increased DA levels to approximately 200 to 400% of control values. Finally, cumulatively administered MA produced comparable changes in DA levels in both naive and 0.3 mg/kg MA-trained rats. These latter results suggest that sensitization of DA release does not play a prominent role in the discriminative stimulus effects of psychomotor stimulants.

Footnotes

  • This work was supported by in part by the National Institutes of Health National Institute on Drug Abuse [Grants R01-DA07658, R01-DA10566] (to J.B.) and the Ruth L. Kirschstein National Service Award (to Nancy K. Mello).

  • Article, publication date, and citation information can be found at http://jpet.aspetjournals.org.

    doi:10.1124/jpet.110.165746.

  • ABBREVIATIONS:

    MA
    methamphetamine
    COC
    cocaine
    DA
    dopamine
    GBR 12909
    1-[2-[bis(4-fluorophenyl-)methoxy]ethyl]-4-(3-phenylpropyl)piperazine
    NAcb
    nucleus accumbens
    FR
    fixed-ratio
    LED
    light-emitting diode
    TO
    timeout
    ANOVA
    analysis of variance.

  • Received January 8, 2010.
  • Accepted February 22, 2010.
  • Copyright © 2010 by The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 389 (1)
Journal of Pharmacology and Experimental Therapeutics
Vol. 389, Issue 1
1 Apr 2024
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Research ArticleBEHAVIORAL PHARMACOLOGY

Monoaminergic Psychomotor Stimulants: Discriminative Stimulus Effects and Dopamine Efflux

Rajeev I. Desai, Carol A. Paronis, Jared Martin, Ramya Desai and Jack Bergman
Journal of Pharmacology and Experimental Therapeutics June 1, 2010, 333 (3) 834-843; DOI: https://doi.org/10.1124/jpet.110.165746

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Research ArticleBEHAVIORAL PHARMACOLOGY

Monoaminergic Psychomotor Stimulants: Discriminative Stimulus Effects and Dopamine Efflux

Rajeev I. Desai, Carol A. Paronis, Jared Martin, Ramya Desai and Jack Bergman
Journal of Pharmacology and Experimental Therapeutics June 1, 2010, 333 (3) 834-843; DOI: https://doi.org/10.1124/jpet.110.165746
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