Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 May;117(3):420-441.
doi: 10.1002/jeab.744. Epub 2022 Mar 1.

Clinical neuropharmacology of cocaine reinforcement: A narrative review of human laboratory self-administration studies

Affiliations
Review

Clinical neuropharmacology of cocaine reinforcement: A narrative review of human laboratory self-administration studies

Sean D Regnier et al. J Exp Anal Behav. 2022 May.

Abstract

Cocaine use is an unrelenting public health concern. To inform intervention and prevention efforts, it is crucial to develop an understanding of the clinical neuropharmacology of the reinforcing effects of cocaine. The purpose of this review is to evaluate and synthesize human laboratory studies that assess pharmacological manipulations of cocaine self-administration. Forty-one peer-reviewed, human cocaine self-administration studies in which participants received a pretreatment drug were assessed. The pharmacological action and treatment regimen for all drugs reviewed were considered. Drugs that increase extracellular dopamine tend to have the most consistent effects on cocaine self-administration. The ability of nondopaminergic drugs to impact cocaine reinforcement might be related to their downstream effects on dopamine, though it is difficult to draw conclusions because pharmacologically selective compounds are not widely available for human testing. The ability of acute versus chronic drug treatment to differentially affect human cocaine self-administration was not determined because buprenorphine was the only pretreatment drug that was assessed under both acute and chronic dosing regimens. Future research directly comparing acute and chronic drug treatment and/or comparing drugs with different mechanisms of action, is needed to make more conclusive determinations about the clinical neuropharmacology of cocaine reinforcement.

Keywords: cocaine; humans; neuropharmacology; pretreatment; self-administration.

PubMed Disclaimer

References

    1. Aigner TG, & Balster RL (1978). Choice behavior in rhesus monkeys: cocaine versus food. Science, 201(4355), 534–535. 10.1126/science.96531 - DOI - PubMed
    1. Baker DA, McFarland K, Lake RW, Shen H, Toda S, & Kalivas PW (2003). N-acetyl cysteine-induced blockade of cocaine-induced reinstatement. Annals of the New York Academy of Sciences, 1003, 349–351. 10.1196/annals.1300.023 - DOI - PubMed
    1. Banks ML, Blough BE, Fennell TR, Snyder RW, & Negus SS (2013). Effects of phendimetrazine treatment on cocaine vs food choice and extended-access cocaine consumption in rhesus monkeys. Neuropsychopharmacology, 38(13), 2698–2707. 10.1038/npp.2013.180 - DOI - PMC - PubMed
    1. Bolin BL, Lile JA, Marks KR, Beckmann JS, Rush CR, & Stoops WW (2016). Buspirone reduces sexual risk-taking intent but not cocaine self-administration. Experimental and Clinical Psychopharmacology, 24(3), 162–173. 10.1037/pha0000076 - DOI - PMC - PubMed
    1. Caine SB, Negus SS, Mello NK, Patel S, Bristow L, Kulagowski J, Vallone D, Saiardi A, & Borrelli E (2002). Role of dopamine D2-like receptors in cocaine self-administration: Studies with D2 receptor mutant mice and novel D2 receptor antagonists. Journal of Neuroscience, 22(7), 2977–2988. https://doi.org/20026264 - PMC - PubMed

Publication types

LinkOut - more resources