Literature DB >> 34413199

Influence of Contingent and Noncontingent Drug Histories on the Development of High Levels of MDPV Self-Administration.

Michelle R Doyle1, Agnieszka Sulima1, Kenner C Rice1, Gregory T Collins2.   

Abstract

A subset of rats that self-administer 3,4-methylenedioxypyrovalerone (MDPV) develop unusually high levels of drug taking. A history of responding maintained by cocaine, but not food, prevents the development of this high-responder phenotype; however, it is unclear how histories of noncontingent cocaine exposure or self-administering drugs from other pharmacological classes would affect its development. In the current studies, 5 groups of male Sprague-Dawley rats were used to determine whether histories of responding maintained by drugs from different pharmacological classes (e.g., MDPV, cocaine, fentanyl, nicotine, or ketamine) would differentially impact the development of the high-responder phenotype when MDPV was available for self-administration. Two additional groups were used to determine whether noncontingent exposure to cocaine would prevent the development of the high-responder phenotype when MDPV was available for self-administration, and whether noncontingent exposure to MDPV would facilitate the development of the high-responder phenotype when cocaine was available for self-administration. Consistent with previous reports, a history of response-contingent cocaine, and to a lesser extent noncontingent cocaine, prevented the MDPV high-responder phenotype; however, when responding was initially maintained by fentanyl, nicotine, or ketamine, the MDPV high-responder phenotype developed in ∼45% of rats. By manipulating behavioral and pharmacological histories prior to evaluating MDPV self-administration, the current studies provide additional evidence that a history of response-contingent (or noncontingent) cocaine can prevent the transition from well regulated to aberrant drug-taking when responding is maintained by MDPV. Although the mechanism(s) that underlies this novel high-responder phenotype are unknown, elucidation may provide insight into individual differences relating to substance use disorder. SIGNIFICANCE STATEMENT: A subset of outbred Sprague-Dawley rats self-administer high levels of the synthetic cathinone 3,4-methylenedioxypyrovalerone (MDPV). Understanding the behavioral and/or pharmacological factors that can prevent the development of dysregulated MDPV self-administration may provide insight into individual differences in vulnerability to develop a substance use disorder.
Copyright © 2021 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2021        PMID: 34413199      PMCID: PMC8626776          DOI: 10.1124/jpet.121.000655

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  46 in total

1.  Drug and reinforcement history as determinants of the response-maintaining effects of quinpirole in the rat.

Authors:  Gregory T Collins; James H Woods
Journal:  J Pharmacol Exp Ther       Date:  2007-08-03       Impact factor: 4.030

2.  The motivation to self-administer is increased after a history of spiking brain levels of cocaine.

Authors:  Benjamin A Zimmer; Erik B Oleson; David Cs Roberts
Journal:  Neuropsychopharmacology       Date:  2012-03-28       Impact factor: 7.853

3.  Cristalius: a case in designer drugs.

Authors:  Jared Lenz; Jaime Brown; Seth Flagg; Robert Oh; Kenneth Batts; Thomas Ditzler; Jeremy Johnson
Journal:  Mil Med       Date:  2013-07       Impact factor: 1.437

4.  Potent rewarding and reinforcing effects of the synthetic cathinone 3,4-methylenedioxypyrovalerone (MDPV).

Authors:  Lucas R Watterson; Peter R Kufahl; Natali E Nemirovsky; Kaveish Sewalia; Megan Grabenauer; Brian F Thomas; Julie A Marusich; Scott Wegner; M Foster Olive
Journal:  Addict Biol       Date:  2012-07-11       Impact factor: 4.280

Review 5.  Feeding and reward: perspectives from three rat models of binge eating.

Authors:  Rebecca L Corwin; Nicole M Avena; Mary M Boggiano
Journal:  Physiol Behav       Date:  2011-05-01

6.  Temporal pattern of cocaine intake determines tolerance vs sensitization of cocaine effects at the dopamine transporter.

Authors:  Erin S Calipari; Mark J Ferris; Benjamin A Zimmer; David C S Roberts; Sara R Jones
Journal:  Neuropsychopharmacology       Date:  2013-05-30       Impact factor: 7.853

Review 7.  Differential pharmacokinetics and pharmacodynamics of methylphenidate enantiomers: does chirality matter?

Authors:  John S Markowitz; Kennerly S Patrick
Journal:  J Clin Psychopharmacol       Date:  2008-06       Impact factor: 3.153

8.  Nicotine-like behavioral effects of the minor tobacco alkaloids nornicotine, anabasine, and anatabine in male rodents.

Authors:  S Barak Caine; Gregory T Collins; Morgane Thomsen; Curtis Wright; Ryan K Lanier; Nancy K Mello
Journal:  Exp Clin Psychopharmacol       Date:  2014-02       Impact factor: 3.157

9.  Reinforcing effects of synthetic cathinones in rhesus monkeys: Dose-response and behavioral economic analyses.

Authors:  Fernando B de Moura; Alexander Sherwood; Thomas E Prisinzano; Carol A Paronis; Jack Bergman; Stephen J Kohut
Journal:  Pharmacol Biochem Behav       Date:  2021-01-12       Impact factor: 3.533

10.  Drug seeking becomes compulsive after prolonged cocaine self-administration.

Authors:  Louk J M J Vanderschuren; Barry J Everitt
Journal:  Science       Date:  2004-08-13       Impact factor: 47.728

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