Evidence map›Paper›PMID 31259593›Full record

ArticleExperimental and clinical psychopharmacology2020

Pharmacological validation of a translational model of cocaine use disorder: Effects of d-amphetamine maintenance on choice between intravenous cocaine and a nondrug alternative in humans and rhesus monkeys.

Joshua A Lile, Amy R Johnson, Matthew L Banks, Kevin W Hatton, Lon R Hays, Katherine L Nicholson, Justin L Poklis, Abner O Rayapati, Craig R Rush, William W Stoops and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Experimental and clinical psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
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  3. Open-label pilot study of lisdexamfetamine for cocaine use disorder.The American journal of drug and alcohol abuse · 2021
    Trial
  4. Article
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  13. Effects of naltrexone on amphetamine choice in rhesus monkeys and rats.Experimental and clinical psychopharmacology · 2023
    Article
  14. Article
  15. Review
  16. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Joshua A LileDepartment of Behavioral Science, University of Kentucky College of Medicine.
Amy R JohnsonDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center.
Matthew L BanksDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center.
Kevin W HattonDepartment of Anesthesiology, University of Kentucky College of Medicine.
Lon R HaysDepartment of Psychiatry, University of Kentucky College of Medicine.
Katherine L NicholsonDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center.
Justin L PoklisDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center.
Abner O RayapatiDepartment of Psychiatry, University of Kentucky College of Medicine.
Craig R RushDepartment of Behavioral Science, University of Kentucky College of Medicine.
William W StoopsDepartment of Behavioral Science, University of Kentucky College of Medicine.
S Stevens NegusDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center.
University of Kentucky · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
TRAINING IN THE PHARMACOLOGY OF ABUSED DRUGST32DA007027 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI William L. Dewey · 1985 to 2026
$14.7M
VCU Center for Drug Addiction ResearchP30DA033934 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOLENE J WINDLE · 2014 to 2026
$13.8M
RESEARCH TRAINING IN DRUG ABUSE BEHAVIORT32DA007304 · NIDA · UNIVERSITY OF KENTUCKY · PI RUSH, CRAIG R · 1998 to 2012
$3.1M
A translational determination of the mechanisms of maladaptive choice in cocaine use disorderR01DA045023 · NIDA · UNIVERSITY OF KENTUCKY · PI BECKMANN, JOSHUA, LILE, JOSHUA ANTHONY · 2018 to 2022
$3.0M
Medications Development for Cocaine: A Translational Approach in Monkey and HumanR01DA033364 · NIDA · UNIVERSITY OF KENTUCKY · PI LILE, JOSHUA ANTHONY · 2013 to 2016
$1.9M
NCATS NIH HHS UL1 TR001998NIDA NIH HHS P30 DA033934NIDA NIH HHS R01 DA033364NIDA NIH HHS R01 DA045023NIDA NIH HHS T32 DA007027NIDA NIH HHS T32 DA007304NIH HHS
6 · The paper itself

Abstract

Drug self-administration procedures are the gold standard for laboratory research to study mechanisms of drug use disorders and evaluate candidate medications. However, preclinical-to-clinical translation has been hampered by a lack of coordination. To address this limitation, we previously developed homologous intravenous (IV) cocaine choice self-administration procedures in rhesus monkeys and humans, and then demonstrated their functional equivalence. The present studies sought to determine the sensitivity of these procedures to d-amphetamine maintenance. Three (N = 3) rhesus monkeys with histories of cocaine self-administration and 16 (N = 16) humans with cocaine use disorder completed the studies. Monkeys were maintained on IV d-amphetamine (0, 0.019, 0.037 and 0.074 mg/kg/h), and then completed 7 sessions during each condition in which they completed 9 choice trials to receive 0.14 mg/kg/injection IV cocaine (corresponding to 10 mg/70 kg in humans) or 10 food pellets under independent, concurrent progressive-ratio schedules. Humans were maintained on oral extended release d-amphetamine (0, 30 and 60 mg/day, corresponding to the lowest 3 doses in monkeys) and participated in 12 sessions in which they chose money ($6.00) or IV cocaine (0, 3, 10 and 30 mg/70 kg). Blood samples were taken to compare d-amphetamine plasma levels across species. In monkeys and humans, d-amphetamine reduced the number of cocaine choices and produced comparable blood levels at equivalent daily doses. d-Amphetamine had similar efficacy, though lower potency, at reducing choice for an equivalent cocaine dose in monkeys relative to humans. These coordinated studies support the utility of these procedures as a translational model for cocaine use disorder. (PsycInfo Database Record (c) 2020 APA, all rights reserved).

Indexed as

Administration, IntravenousAdolescentAdultAnimalsChoice BehaviorCocaineCocaine-Related DisordersDextroamphetamineFemaleHumansMacaca mulattaMaleMiddle AgedSelf AdministrationYoung AdultCocaineDextroamphetamine

Identifiers

PMID31259593
PMCPMC6938584
OpenAlexW2955514859

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.