Evidence map›Paper›PMID 32464226›Full record

ArticleNeurochemistry international2020

Glucagon-like peptide-1 receptor regulation of basal dopamine transporter activity is species-dependent.

Mathias E Jensen, Aurelio Galli, Morgane Thomsen, Kathrine L Jensen, Gerda K Thomsen, Mette K Klausen, Tina Vilsbøll, Mikkel B Christensen, Jens J Holst, Anthony Owens and 6 more

Open access · greenAbstract read
In one paragraph

Article in Neurochemistry international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 28% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  10. Effects of GLP-1 Receptor Agonists in Alcohol Use Disorder.Basic & clinical pharmacology & toxicology · 2025
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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

16 authors at 6 institutions in 2 countries.

Mathias E JensenPsychiatric Centre Copenhagen, University Hospital of Copenhagen, Denmark. Electronic address: mathias.ebbesen.jensen.01@regionh.dk.
Aurelio GalliDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Morgane ThomsenPsychiatric Centre Copenhagen, University Hospital of Copenhagen, Denmark.
Kathrine L JensenMolecular Neuropharmacology and Genetics Laboratory, Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Gerda K ThomsenNeurobiology Research Unit, Neuroscience Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Mette K KlausenPsychiatric Centre Copenhagen, University Hospital of Copenhagen, Denmark.
Tina VilsbøllDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Steno Diabetes Center Copenhagen, Gentofte Hospital, Denmark.
Mikkel B ChristensenDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Clinical Pharmacology, Bispebjerg Hospital, University of Copenhagen, Denmark.
Jens J HolstNovo Nordisk Foundation Center for Basic Metabolic Research Endocrinology and Metabolism, Copenhagen, Denmark.
Anthony OwensDepartment of Cellular and Integrative Physiology, University of Texas Health Science Center at San Antonio, USA.
Sabrina RobertsonDepartment of Psychology and Neuroscience, University of North Carolina at Chapel Hill, USA.
Lynette DawsDepartment of Cellular and Integrative Physiology, University of Texas Health Science Center at San Antonio, USA.
Daniele ZanellaDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Ulrik GetherMolecular Neuropharmacology and Genetics Laboratory, Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Gitte M KnudsenNeurobiology Research Unit, Neuroscience Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anders Fink-JensenPsychiatric Centre Copenhagen, University Hospital of Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKCopenhagen University Hospital · DKThe University of Texas Health Science Center at San Antonio · USUniversity of Alabama at Birmingham · USNovo Nordisk Foundation · DKUniversity of North Carolina at Chapel Hill · US

Funding

University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
Mechanisms Regulating Serotonin Clearance In Vivo: Studies Using KO MiceR01MH064489 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DAWS, LYNETTE C · 2002 to 2011
$3.0M
Glucagon-like peptide-1 modulation of alcohol effectsR01AA025071 · NIAAA · REGION HOVEDSTADEN · PI THOMSEN, MORGANE HERMANN · 2017 to 2022
$627k
Bile acid signaling as a pharmacological target for the treatment of cocaine abuseR21DA043960 · NIDA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FLYNN, CHARLES R, GALLI, AURELIO · 2018 to 2019
$383k
Mechanisms regulating serotonin clearance in vivo: Studies using KO miceR56MH064489 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DAWS, LYNETTE C · 2014 to 2014
$372k
NIAAA NIH HHS R01 AA025071NIDA NIH HHS R21 DA043960NIDDK NIH HHS P30 DK079626NIMH NIH HHS R01 MH064489NIMH NIH HHS R56 MH064489
6 · The paper itself

Abstract

introductionA solid body of preclinical evidence shows that glucagon-like peptide-1 receptor (GLP-1R) agonists attenuate the effects of substance use disorder related behaviors. The mechanisms underlying these effects remain elusive. In the present study, we hypothesized that GLP-1R activation modulates dopaminetransporter (DAT) and thus dopamine (DA) homeostasis in striatum. This was evaluated in three different experiments: two preclinical and one clinical.

methodsRat striatal DA uptake, DA clearance and DAT cell surface expression was assessed following GLP-1 (7-36)-amide exposure in vitro. DA uptake in mice was assesed ex vivo following systemic treatment with the GLP-1R agonist exenatide. In addition, DA uptake was measured in GLP-1R knockout mice and compared with DA-uptake in wild type mice. In healthy humans, changes in DAT availability was assessed during infusion of exenatide measured by single-photon emission computed tomography imaging.

resultsIn rats, GLP-1 (7-36)-amide increased DA uptake, DA clearance and DAT cell surface expression in striatum. In mice, exenatide did not change striatal DA uptake. In GLP-1R knockout mice, DA uptake was similar to what was measured in wildtype mice. In humans, systemic infusion of exenatide did not result in acute changes in striatal DAT availability.

conclusionsThe GLP-1R agonist-induced modulation of striatal DAT activity in vitro in rats could not be replicated ex vivo in mice and in vivo in humans. Therefore, the underlying mechanisms of action for the GLP-1R agonists-induced efficacy in varios addiction-like behavioural models still remain.

Indexed as

AdolescentAdultAnimalsCorpus StriatumDopamineDopamine AntagonistsDopamine Plasma Membrane Transport ProteinsExenatideFemaleGlucagon-Like Peptide 1HumansMaleMiceMice, Inbred C57BLMice, KnockoutOrgan Culture TechniquesDopamineDopamine AntagonistsDopamine Plasma Membrane Transport ProteinsExenatideGlucagon-Like Peptide 1glucagon-like peptide 1 (7-36), Val(8)-Peptide FragmentsAddictionDopamine transporterDopamine uptakeGlucagon-like peptide-1Striatum

Identifiers

PMID32464226
PMCPMC7452124
OpenAlexW3031242059

What OpenQuestion holds

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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.