Evidence map›Paper›PMID 27269368›Full record

Trial reportDrug and alcohol dependence2016

Development of a translational model to screen medications for cocaine use disorder II: Choice between intravenous cocaine and money in humans.

Joshua A Lile, William W Stoops, Craig R Rush, S Stevens Negus, Paul E A Glaser, Kevin W Hatton, Lon R Hays

Abstract readClinical Trial
In one paragraph

Trial report in Drug and alcohol dependence, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

37 citing papers in PubMed, 46 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Joshua A LileDepartment of Behavioral Science, University of Kentucky College of Medicine, Medical Behavioral Science Building, 1100 Veterans Dr., Lexington, KY 40536-0086, United States; Department of Psychology, University of Kentucky College of Arts and Sciences, Kastle Hall, Lexington, KY 40506-0044, United States; Department of Psychiatry, University of Kentucky College of Medicine, 3470 Blazer Pkwy, Lexington, KY 40509-1810, United States. Electronic address: jalile2@email.uky.edu.
William W StoopsDepartment of Behavioral Science, University of Kentucky College of Medicine, Medical Behavioral Science Building, 1100 Veterans Dr., Lexington, KY 40536-0086, United States; Department of Psychology, University of Kentucky College of Arts and Sciences, Kastle Hall, Lexington, KY 40506-0044, United States; Department of Psychiatry, University of Kentucky College of Medicine, 3470 Blazer Pkwy, Lexington, KY 40509-1810, United States.
Craig R RushDepartment of Behavioral Science, University of Kentucky College of Medicine, Medical Behavioral Science Building, 1100 Veterans Dr., Lexington, KY 40536-0086, United States; Department of Psychology, University of Kentucky College of Arts and Sciences, Kastle Hall, Lexington, KY 40506-0044, United States; Department of Psychiatry, University of Kentucky College of Medicine, 3470 Blazer Pkwy, Lexington, KY 40509-1810, United States.
S Stevens NegusDepartment of Pharmacology and Toxicology, Virginia Commonwealth University Medical Center, 410 N. 12th St., Richmond, VA 23298-0613, United States.
Paul E A GlaserDepartment of Psychiatry, University of Kentucky College of Medicine, 3470 Blazer Pkwy, Lexington, KY 40509-1810, United States; Department of Psychiatry, Washington University School of Medicine in St. Louis, 660 S. Euclid Ave., St. Louis, MO 6311, United States.
Kevin W HattonDepartment of Anesthesiology, University of Kentucky College of Medicine, Chandler Medical Center, 800 Rose St., Lexington, KY 40536, United States; Department of Surgery, University of Kentucky College of Medicine, Chandler Medical Center, 800 Rose St., Lexington, KY 40536, United States.
Lon R HaysDepartment of Psychiatry, University of Kentucky College of Medicine, 3470 Blazer Pkwy, Lexington, KY 40509-1810, United States; Department of Internal Medicine, University of Kentucky College of Medicine, University Health Service, 830 South Limestone, Lexington, KY 40536-0284, United States.
University of Kentucky · USAlbert B. Chandler Hospital · USVirginia Commonwealth University Medical Center · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
Medications Development for Cocaine: A Translational Approach in Monkey and HumanR01DA033364 · NIDA · UNIVERSITY OF KENTUCKY · PI LILE, JOSHUA ANTHONY · 2013 to 2016
$1.9M
Medications Development for Cannabis-Use Disorders: Clinical StudiesK02DA031766 · NIDA · UNIVERSITY OF KENTUCKY · PI LILE, JOSHUA ANTHONY · 2011 to 2015
$487k
NCATS NIH HHS UL1 TR000117NIDA NIH HHS K02 DA031766NIDA NIH HHS R01 DA033364
6 · The paper itself

Abstract

backgroundA medication for treating cocaine use disorder has yet to be approved. Laboratory-based evaluation of candidate medications in animals and humans is a valuable means to demonstrate safety, tolerability and initial efficacy of potential medications. However, animal-to-human translation has been hampered by a lack of coordination. Therefore, we designed homologous cocaine self-administration studies in rhesus monkeys (see companion article) and human subjects in an attempt to develop linked, functionally equivalent procedures for research on candidate medications for cocaine use disorder.

methodsEight (N=8) subjects with cocaine use disorder completed 12 experimental sessions in which they responded to receive money ($0.01, $1.00 and $3.00) or intravenous cocaine (0, 3, 10 and 30mg/70kg) under independent, concurrent progressive-ratio schedules. Prior to the completion of 9 choice trials, subjects sampled the cocaine dose available during that session and were informed of the monetary alternative value.

resultsThe allocation of behavior varied systematically as a function of cocaine dose and money value. Moreover, a similar pattern of cocaine choice was demonstrated in rhesus monkeys and humans across different cocaine doses and magnitudes of the species-specific alternative reinforcers. The subjective and cardiovascular responses to IV cocaine were an orderly function of dose, although heart rate and blood pressure remained within safe limits.

conclusionsThese coordinated studies successfully established drug versus non-drug choice procedures in humans and rhesus monkeys that yielded similar cocaine choice behavior across species. This translational research platform will be used in future research to enhance the efficiency of developing interventions to reduce cocaine use.

Indexed as

Administration, IntravenousAdultAnimalsBlood PressureChoice BehaviorCocaineCocaine-Related DisordersDose-Response Relationship, DrugHeart RateHumansMacaca mulattaMaleMiddle AgedReinforcement, PsychologyReinforcement ScheduleSelf AdministrationCocaineCardiovascularChoiceMonkeyProgressive-ratioReinforcing effectsReverse translationSubjective effects

Identifiers

PMID27269368
PMCPMC4939714
OpenAlexW2398424572

What OpenQuestion holds

Textmetadata
LicenceTDM
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.