Evidence map›Paper›PMID 26044906›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

The Novel μ-Opioid Receptor Antagonist GSK1521498 Decreases Both Alcohol Seeking and Drinking: Evidence from a New Preclinical Model of Alcohol Seeking.

Chiara Giuliano, Charles R Goodlett, Daina Economidou, Maria P García-Pardo, David Belin, Trevor W Robbins, Edward T Bullmore, Barry J Everitt

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Total-body imaging of mu-opioid receptors with [European journal of nuclear medicine and molecular imaging · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Compulsive Alcohol Seeking Results from a Failure to Disengage Dorsolateral Striatal Control over Behavior.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Anterior Insular Cortex is Critical for the Propensity to Relapse Following Punishment-Imposed Abstinence of Alcohol Seeking.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  16. Understanding Addiction Using Animal Models.Frontiers in behavioral neuroscience · 2019
    Article
  17. Addictive behaviour in experimental animals: prospects for translation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  18. Compulsive Seekers: Our take. Two Clinicians' Perspective on a New Animal Model of Addiction.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  19. Evidence for a Long-Lasting Compulsive Alcohol Seeking Phenotype in Rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Chiara GiulianoBehavioral and Clinical Neuroscience Institute and Department of Psychology, University of Cambridge, Cambridge, UK.
Charles R GoodlettDepartment of Psychology, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Daina EconomidouBehavioral and Clinical Neuroscience Institute and Department of Psychology, University of Cambridge, Cambridge, UK.
Maria P García-PardoUnit of Research Psychobiology of Drug Dependence, Department of Psychobiology, School of Psychology, University of Valencia, Valencia, Spain.
David BelinDepartment of Pharmacology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-7383-372X
Trevor W RobbinsBehavioral and Clinical Neuroscience Institute and Department of Psychology, University of Cambridge, Cambridge, UK.
Edward T BullmoreBehavioral and Clinical Neuroscience Institute and Department of Psychology, University of Cambridge, Cambridge, UK.
Barry J EverittBehavioral and Clinical Neuroscience Institute and Department of Psychology, University of Cambridge, Cambridge, UK.

Funding

Rodents with Genetic Differences in Alcohol PreferenceR24AA015512 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2005 to 2014
$5.1M
Medical Research Council G0001354Medical Research Council G1000183Medical Research Council G1002231NIAAA NIH HHS R24 AA015512
6 · The paper itself

Abstract

Distinct environmental and conditioned stimuli influencing ethanol-associated appetitive and consummatory behaviors may jointly contribute to alcohol addiction. To develop an effective translational animal model that illuminates this interaction, daily seeking responses, maintained by alcohol-associated conditioned stimuli (CSs), need to be dissociated from alcohol drinking behavior. For this, we established a procedure whereby alcohol seeking maintained by alcohol-associated CSs is followed by a period during which rats have the opportunity to drink alcohol. This cue-controlled alcohol-seeking procedure was used to compare the effects of naltrexone and GSK1521498, a novel selective μ-opioid receptor antagonist, on both voluntary alcohol-intake and alcohol-seeking behaviors. Rederived alcohol-preferring, alcohol-nonpreferring, and high-alcohol-drinking replicate 1 line of rats (Indiana University) first received 18 sessions of 24 h home cage access to 10% alcohol and water under a 2-bottle choice procedure. They were trained subsequently to respond instrumentally for access to 15% alcohol under a second-order schedule of reinforcement, in which a prolonged period of alcohol-seeking behavior was maintained by contingent presentations of an alcohol-associated CS acting as a conditioned reinforcer. This seeking period was terminated by 20 min of free alcohol drinking access that achieved significant blood alcohol concentrations. The influence of pretreatment with either naltrexone (0.1-1-3 mg/kg) or GSK1521498 (0.1-1-3 mg/kg) before instrumental sessions was measured on both seeking and drinking behaviors, as well as on drinking in the 2-bottle choice procedure. Naltrexone and GSK1521498 dose-dependently reduced both cue-controlled alcohol seeking and alcohol intake in the instrumental context as well as alcohol intake in the choice procedure. However, GSK1521498 showed significantly greater effectiveness than naltrexone, supporting its potential use for promoting abstinence and preventing relapse in alcohol addiction.

Indexed as

Alcohol DeterrentsAlcohol DrinkingAlcohol-Related DisordersAnimalsBlood Alcohol ContentChoice BehaviorConditioning, OperantCuesDisease Models, AnimalDose-Response Relationship, DrugDrug Evaluation, PreclinicalDrug-Seeking BehaviorIndansMaleNaltrexoneNarcotic AntagonistsAlcohol DeterrentsBlood Alcohol ContentIndansN-((3,5-difluoro-3'-(1H-1,2,4-triazol-3-yl)-4-biphenylyl)methyl)-2,3-dihydro-1H-inden-2-amineNaltrexoneNarcotic AntagonistsReceptors, Opioid, muTriazoles

Identifiers

PMID26044906
PMCPMC4864633

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.