Evidence map›Paper›PMID 30382353›Full record

ArticlePsychopharmacology2019

Effects of glucagon-like peptide 1 analogs on alcohol intake in alcohol-preferring vervet monkeys.

Morgane Thomsen, Jens Juul Holst, Anna Molander, Kristian Linnet, Maurice Ptito, Anders Fink-Jensen

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 57 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 4 pooled it
3.1field-weighted citation impact, top 7% 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

57 citing papers in PubMed, 4 syntheses or guidelines pooled it, 86 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Morgane ThomsenLaboratory of Neuropsychiatry, Psychiatric Centre Copenhagen and University Hospital of Copenhagen, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Jens Juul HolstNNF Center for Basic Metabolism Research and Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anna MolanderLaboratory of Neuropsychiatry, Psychiatric Centre Copenhagen and University Hospital of Copenhagen, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Kristian LinnetSection of Forensic Chemistry, Department of Forensic Medicines, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Maurice PtitoSchool of Optometry, University of Montreal, QC, Canada.
Anders Fink-JensenLaboratory of Neuropsychiatry, Psychiatric Centre Copenhagen and University Hospital of Copenhagen, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark. anders.fink-jensen@regionh.dk.ORCID http://orcid.org/0000-0001-7143-1236
University of Copenhagen · DKCopenhagen University Hospital · DKCaribbean Research and Management of Biodiversity Foundation · CW

Funding

Glucagon-like peptide-1 modulation of alcohol effectsR01AA025071 · NIAAA · REGION HOVEDSTADEN · PI THOMSEN, MORGANE HERMANN · 2017 to 2022
$627k
National Institute on Alcohol Abuse and Alcoholism R01AA025071NIAAA NIH HHS R01 AA025071
6 · The paper itself

Abstract

backgroundPreclinical studies in rodents have demonstrated inhibitory effects of glucagon-like peptide-1 (GLP-1) receptor stimulation on alcohol consumption. The effects of GLP-1 receptor stimulation on alcohol intake in primates have not been investigated.

methodsWe performed placebo-controlled studies on the effects of the GLP-1 receptor agonists exenatide and liraglutide on alcohol consumption in alcohol-preferring male African vervet monkeys. Monkeys selected for voluntary alcohol drinking were observed for at least 10 days of baseline drinking and allocated to drug or vehicle (n = 11-12 per group) balanced with respect to alcohol intake. Monkeys had access to alcohol 4 h/day. In a first study, monkeys were treated with exenatide 0.04 mg/kg or vehicle once weekly for 5 weeks to obtain steady-state plasma levels. In a second study, monkeys were treated daily with liraglutide (increasing dosing, 10 to 50 μg/kg/day) or vehicle over 2 weeks. In both studies, access to alcohol was suspended during drug up-titration. Then, alcohol was again made available 4 h/day and treatment was continued for 2 weeks, during which alcohol intake was recorded. Observation of alcohol intake was continued for a week of drug washout.

resultsLiraglutide and to a lesser extent exenatide significantly reduced alcohol consumption without causing any signs of emesis and with no effect on water intake as compared to vehicle.

conclusionsThe present study demonstrates for the first time that GLP-1 receptor agonists can reduce voluntary alcohol drinking in non-human primates. The data substantiate the potential usefulness of GLP-1 receptor agonists in the treatment of alcohol use disorder.

Indexed as

Alcohol DrinkingGlucagon-Like Peptide-1 Receptor AgonistsAnimalsBehavior, AnimalCentral Nervous System DepressantsChlorocebus aethiopsDrinkingEthanolExenatideGlucagon-Like Peptide 1HumansLiraglutideMaleSelf AdministrationWaterCentral Nervous System DepressantsEthanolExenatideGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsLiraglutideWaterAlcohol use disorderExendin-4GLP-1LiraglutideNon-human primatePharmacotherapy

Identifiers

PMID30382353
PMCPMC6428196
OpenAlexW2899078909

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.