Evidence map›Paper›PMID 29109060›Full record

ArticleNeuropharmacology2018

Cannabinoid-1 receptor neutral antagonist reduces binge-like alcohol consumption and alcohol-induced accumbal dopaminergic signaling.

Andrea Balla, Bin Dong, Borehalli M Shilpa, Kiran Vemuri, Alexandros Makriyannis, Subhash C Pandey, Henry Sershen, Raymond F Suckow, K Yaragudri Vinod

Open access · bronzeAbstract read
In one paragraph

Article in Neuropharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. CBMolecular psychiatry · 2026
    Article
  5. Article
  6. AM6527, a neutral CB1 receptor antagonist, suppresses opioid taking and seeking, as well as cocaine seeking in rodents without aversive effects.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  17. Reduced Motivation in Perinatal Fluoxetine-Treated Mice: A Hypodopaminergic Phenotype.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
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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

9 authors at 4 institutions in 1 country.

Andrea BallaDepartment of Neurochemistry, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States.
Bin DongDivision of Analytical Psychopharmacology, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States.
Borehalli M ShilpaDivision of Analytical Psychopharmacology, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States.
Kiran VemuriCenter for Drug Discovery, Northeastern University, Boston, MA, United States.
Alexandros MakriyannisCenter for Drug Discovery, Northeastern University, Boston, MA, United States.
Subhash C PandeyCenter for Alcohol Research in Epigenetics, Department of Psychiatry, University of Illinois at Chicago and Jesse Brown VA Medical Center, Chicago, IL, United States.
Henry SershenDepartment of Neurochemistry, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States; Department of Psychiatry, NYU Langone Medical Center, New York, NY, United States.
Raymond F SuckowDivision of Analytical Psychopharmacology, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States; New York State Psychiatric Institute, New York, United States; Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, NY, United States.
K Yaragudri VinodDivision of Analytical Psychopharmacology, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, NY, United States; Emotional Brain Institute, Orangeburg, New York, NY, United States; Department of Child and Adolescent Psychiatry, NYU Langone Medical Center, New York, NY, United States. Electronic address: vyaragudri@nki.rfmh.org.
Nathan Kline Institute for Psychiatric Research · USNortheastern University · USJesse Brown VA Medical Center · USNYU Langone Health · US

Funding

Role of the CB1 receptor signaling in alcohol consumptionR01AA021662 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PANDEY, SUBHASH C., YARAGUDRI, VINOD K · 2014 to 2017
$1.4M
Role of the Endocannabinoid Signaling in Fetal Alcohol Spectrum DisordersR21AA018709 · NIAAA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI YARAGUDRI, VINOD K · 2011 to 2012
$400k
NIAAA NIH HHS R01 AA021662NIAAA NIH HHS R21 AA018709
6 · The paper itself

Abstract

Binge alcohol (ethanol) drinking is associated with profound adverse effects on our health and society. Rimonabant (SR141716A), a CB1 receptor inverse agonist, was previously shown to be effective for nicotine cessation and obesity. However, studies using rimonabant were discontinued as it was associated with an increased risk of depression and anxiety. In the present study, we examined the pharmacokinetics and effects of AM4113, a novel CB1 receptor neutral antagonist on binge-like ethanol drinking in C57BL/6J mice using a two-bottle choice drinking-in-dark (DID) paradigm. The results indicated a slower elimination of AM4113 in the brain than in plasma. AM4113 suppressed ethanol consumption and preference without having significant effects on body weight, ambulatory activity, preference for tastants (saccharin and quinine) and ethanol metabolism. AM4113 pretreatment reduced ethanol-induced increase in dopamine release in nucleus accumbens. Collectively, these data suggest an important role of CB1 receptor-mediated regulation of binge-like ethanol consumption and mesolimbic dopaminergic signaling, and further points to the potential utility of CB1 neutral antagonists for the treatment of binge ethanol drinking.

Indexed as

Alcohol DrinkingAnalysis of VarianceAnimalsCannabinoid Receptor AntagonistsConditioning, OperantDisease Models, AnimalDopamineEthanolLocomotionMaleMiceMice, Inbred C57BLMicrodialysisNucleus AccumbensPyrazolesReceptor, Cannabinoid, CB1AM4113Cannabinoid Receptor AntagonistsDopamineEthanolPyrazolesReceptor, Cannabinoid, CB1AM4113Binge drinkingCannabinoid receptorNeutral antagonistNucleus accumbens

Identifiers

PMID29109060
PMCPMC5820178
OpenAlexW2766317790

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.