Evidence map›Paper›PMID 26239766›Full record

Trial reportPsychiatry research2015

Dopamine D3 receptor-preferring agonist enhances the subjective effects of cocaine in humans.

Thomas F Newton, Colin N Haile, James J Mahoney, Ravi Shah, Christopher D Verrico, Richard De La Garza, Thomas R Kosten

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychiatry research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Effects of Acute and Chronic Treatments with Dopamine DThe Journal of pharmacology and experimental therapeutics · 2017
    Article
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 2 institutions in 1 country.

Thomas F NewtonBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA. Electronic address: tnewton@bcm.edu.
Colin N HaileBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
James J MahoneyBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
Ravi ShahBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
Christopher D VerricoBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
Richard De La GarzaBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
Thomas R KostenBaylor College of Medicine, Menninger Department of Psychiatry and Behavioral Sciences, & Michael E. DeBakey VA Medical Center, Houston, TX, USA.
Baylor College of Medicine · USMichael E. DeBakey VA Medical Center · US

Funding

Tiagabine and Disulfiram for Cocaine DependenceP50DA018197 · NIDA · YALE UNIVERSITY · PI KOSTEN, THOMAS RICHARD · 2004 to 2013
$12.6M
NIDA NIH HHS P50 DA018197NIDA NIH HHS P50DA018197-10
6 · The paper itself

Abstract

Pramipexole is a D3 dopamine receptor-preferring agonist indicated for the treatment of Parkinson disease. Studies associate pramipexole with pathological gambling and impulse control disorders suggesting a role for D3 receptors in reinforcement processes. Clinical studies showed pramipexole decreased cocaine craving and reversed central deficits in individuals with cocaine use disorder. Preclinical studies have shown acute administration of pramipexole increases cocaine's reinforcing effects whereas other reports suggest chronic pramipexole produces tolerance to cocaine. In a randomized, double-blind, placebo-controlled study we examined the impact of pramipexole treatment on the subjective effects produced by cocaine in volunteers with cocaine use disorder. Volunteers received pramipexole titrated up to 3.0mg/d or placebo over 15 days. Participants then received intravenous cocaine (0, 20 and 40mg) on day 15. Cardiovascular and subjective effects were obtained with visual analog scales at time points across the session. Pramipexole alone increased peak heart rate following saline and diastolic blood pressure following cocaine. Pramipexole produced upwards of two-fold increases in positive subjective effects ratings following cocaine. These results indicate that chronic D3 receptor activation increases the subjective effects of cocaine in humans. Caution should be used when prescribing pramipexole to patients that may also use cocaine.

Indexed as

Reinforcement, PsychologyAdultBenzothiazolesBlood PressureCocaineCocaine-Related DisordersDopamine AgonistsDose-Response Relationship, DrugDouble-Blind MethodDrug SynergismFemaleHumansMaleMiddle AgedPramipexoleReceptors, Dopamine D3BenzothiazolesCocaineDopamine AgonistsPramipexoleReceptors, Dopamine D3Cocaine use disorderDrug reinforcementDrug rewardPeak effectsStimulantsSubstance use disorder

Identifiers

PMID26239766
PMCPMC4584195
OpenAlexW2113998834

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.