Evidence map›Paper›PMID 26429728›Full record

ArticleDrug and alcohol dependence2015

The selective dopamine D3 receptor antagonist, SR 21502, reduces cue-induced reinstatement of heroin seeking and heroin conditioned place preference in rats.

Ewa Galaj, Monica Manuszak, Sandra Babic, Subramaniam Ananthan, Robert Ranaldi

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Trial
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  10. A highly DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  11. Article
  12. Effects of the selective dopamine DBehavioural brain research · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Effect of the dopamine stabilizer (-)-OSU6162 on potentiated incubation of opioid craving after electric barrier-induced voluntary abstinence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  18. Newly Developed Dopamine DThe Journal of pharmacology and experimental therapeutics · 2019
    Article
  19. The highly selective dopamine DNeuropharmacology · 2019
    Article
  20. Dopamine DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    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

5 authors.

Ewa GalajCUNY Graduate Center, New York, NY, United States.
Monica ManuszakQueens College of the City University of New York, Department of Psychology, Flushing, NY, United States.
Sandra BabicQueens College of the City University of New York, Department of Psychology, Flushing, NY, United States.
Subramaniam AnanthanDepartment of Chemistry, Drug Discovery Division, Southern Research Institute, Birmingham, AL, United States.
Robert RanaldiCUNY Graduate Center, New York, NY, United States; Queens College of the City University of New York, Department of Psychology, Flushing, NY, United States. Electronic address: Robert.Ranaldi@qc.cuny.edu.

Funding

Development of Dopamine D3 Ligands as Medications for Psychostimulant AddictionR01DA024675 · NIDA · SOUTHERN RESEARCH INSTITUTE · PI ANANTHAN, SUBRAMANIAM · 2009 to 2011
$1.4M
NIDA NIH HHS R01 DA024675NIDA NIH HHS R01DA024675
6 · The paper itself

Abstract

backgroundBecause the role of dopamine (DA) D3 receptors has been investigated primarily in relation to cocaine-related behaviors little is known of the role of these receptors in heroin seeking. PURPOSES: To investigate the effect of the selective DA D3 receptor antagonist, SR 21502, on cue-induced reinstatement of heroin seeking and heroin conditioned place preference (CPP).

methodsIn experiment 1, rats were trained to self-administer intravenous heroin for 15 days followed by extinction. Following extinction animals were treated with one of several SR 21502 doses (0, 7.5, 10 or 15mg/kg) and a cue-induced reinstatement test was conducted. In experiment 2, animals were conditioned to experience heroin in one compartment of a CPP apparatus and saline in the other. On the test day animals were treated with 0, 3.75, 7.5, 10 or 15mg/kg of SR 21502 and tested for their CPP.

resultsThe results from experiment 1 showed a significant dose-related reduction in cue-induced reinstatement of active lever pressing in the 7.5 and 10mg groups and an absence of the reinstatement effect in the 15mg group. In experiment 2, animals treated with vehicle or 3.75mg of SR 21502 showed significant heroin place preferences but those treated with the higher doses showed no CPP.

conclusionsOur findings suggest that DA D3 receptors play a significant role in heroin approach behaviors driven by conditioned stimuli. As such, we propose that SR 21502 holds potential as an effective pharmacotherapeutic agent for relapse prevention and should be studied further.

Indexed as

CuesAnimalsConditioning, ClassicalDisease Models, AnimalDose-Response Relationship, DrugExtinction, PsychologicalFemaleHeroinHeroin DependenceImidazolesMalePyridinesRatsRats, Long-EvansReceptors, Dopamine D3RecurrenceHeroinImidazolesPyridinesReceptors, Dopamine D3SR 21502AddictionD3 receptor antagonistHeroinReinstatementReward

Identifiers

PMID26429728
PMCPMC4633332

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Registered trials

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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.