Evidence map›Paper›PMID 24584330›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Dopamine D3 receptor is necessary for ethanol consumption: an approach with buspirone.

Gian Marco Leggio, Giovanni Camillieri, Chiara B M Platania, Alessandro Castorina, Giuseppina Marrazzo, Sebastiano Alfio Torrisi, Christina N Nona, Velia D'Agata, José Nobrega, Holger Stark and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 58 citations in OpenAlex.

  1. Substance Addiction Rehabilitation Drugs.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Dopamine: an immune transmitter.Neural regeneration research · 2020
    Review
  10. Review
  11. (±)VK4-40, a novel dopamine DBritish journal of pharmacology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Brain Renin-Angiotensin System Blockade Attenuates Methamphetamine-Induced Hyperlocomotion and Neurotoxicity.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Article
  17. Article
  18. Review
  19. Article
  20. Genes and Alcohol Consumption: Studies with Mutant Mice.International review of neurobiology · 2016
    Review
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

14 authors at 4 institutions in 3 countries.

Gian Marco LeggioDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Giovanni CamillieriDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Chiara B M PlataniaDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Alessandro CastorinaDepartment of Bio-Medical Sciences, Catania University, Catania, Italy.
Giuseppina MarrazzoDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Sebastiano Alfio TorrisiDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Christina N NonaBehavioral Neurobiology Laboratory, Centre for Addiction and Mental Health and Department of Pharmacology and Toxicology, University of Toronto, Toronto, Canada.
Velia D'AgataDepartment of Bio-Medical Sciences, Catania University, Catania, Italy.
José NobregaImaging Research Centre and Campbell Family Research Institute, Centre for Addiction and Mental Health and Departments of Psychiatry, Psychology and Pharmacology, University of Toronto, Toronto, Canada.
Holger StarkInstitute for Pharmaceutical and Medicinal Chemistry, Heinrich-Heine-University Duesseldorf, Duesseldorf, Germany.
Claudio BucoloDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Bernard Le FollTranslational Addiction Research Laboratory, Centre for Addiction and Mental Health and Departments of Family and Community Medicine, Psychiatry and Pharmacology, University of Toronto, Toronto, Canada.
Filippo DragoDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Salvatore SalomoneDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
University of Catania · ITCentre for Addiction and Mental Health · CAHeinrich Heine University Düsseldorf · DEUniversity of Toronto · CA

Funding

Exploring occupancy of dopamine D3 receptor by buspirone in humans using positronR21DA033515 · NIDA · CENTRE FOR ADDICTION AND MENTAL HEALTH · PI BOILEAU, ISABELLE, LE FOLL, BERNARD · 2012 to 2013
$273k
Canadian Institutes of Health ResearchNIDA NIH HHS 1R21DA033515-01
6 · The paper itself

Abstract

Mesolimbic dopamine (DA) controls drug- and alcohol-seeking behavior, but the role of specific DA receptor subtypes is unclear. We tested the hypothesis that D3R gene deletion or the D3R pharmacological blockade inhibits ethanol preference in mice. D3R-deficient mice (D3R(-/-)) and their wild-type (WT) littermates, treated or not with the D3R antagonists SB277011A and U99194A, were tested in a long-term free choice ethanol-drinking (two-bottle choice) and in a binge-like ethanol-drinking paradigm (drinking in the dark, DID). The selectivity of the D3R antagonists was further assessed by molecular modeling. Ethanol intake was negligible in D3R(-/-) and robust in WT both in the two-bottle choice and DID paradigms. Treatment with D3R antagonists inhibited ethanol intake in WT but was ineffective in D3R(-/-) mice. Ethanol intake increased the expression of RACK1 and brain-derived neurotrophic factor (BDNF) in both WT and D3R(-/-); in WT there was also a robust overexpression of D3R. Thus, increased expression of D3R associated with activation of RACK1/BDNF seems to operate as a reinforcing mechanism in voluntary ethanol intake. Indeed, blockade of the BDNF pathway by the TrkB selective antagonist ANA-12 reversed chronic stable ethanol intake and strongly decreased the striatal expression of D3R. Finally, we evaluated buspirone, an approved drug for anxiety disorders endowed with D3R antagonist activity (confirmed by molecular modeling analysis), that resulted effective in inhibiting ethanol intake. Thus, DA signaling via D3R is essential for ethanol-related reward and consumption and may represent a novel therapeutic target for weaning.

Indexed as

Alcohol DrinkingAnimalsBrain-Derived Neurotrophic FactorBuspironeChoice BehaviorCorpus StriatumDrug-Seeking BehaviorEthanolMaleMiceMice, KnockoutNeuropeptidesReceptors, Dopamine D3Receptors for Activated C KinaseBrain-Derived Neurotrophic FactorBuspironeEthanolNeuropeptidesRACK1 protein, mouseReceptors, Dopamine D3Receptors for Activated C Kinase

Identifiers

PMID24584330
PMCPMC4059912
OpenAlexW2007687409

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.