Evidence map›Paper›PMID 33131190›Full record

ArticleBrain and behavior2021

Diabetes type 2 risk gene Dusp8 is associated with altered sucrose reward behavior in mice and humans.

Peter Baumann, Sonja C Schriever, Stephanie Kullmann, Annemarie Zimprich, Andreas Peter, Valerie Gailus-Durner, Helmut Fuchs, Martin Hrabe de Angelis, Wolfgang Wurst, Matthias H Tschöp and 3 more

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. MAP kinase phosphatases in metabolic diseases.Trends in endocrinology and metabolism: TEM · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. A Pathophysiological Intersection of Diabetes and Alzheimer's Disease.International journal of molecular sciences · 2022
    Review
  6. Article
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

13 authors at 4 institutions in 1 country.

Peter BaumannResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, Neuherberg, Germany.
Sonja C SchrieverResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0001-5461-3214
Stephanie KullmannGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Annemarie ZimprichGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0003-2078-6779
Andreas PeterGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Valerie Gailus-DurnerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Helmut FuchsGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Martin Hrabe de AngelisGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Wolfgang WurstInstitute of Developmental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
Matthias H TschöpInstitute for Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany.
Martin HeniGerman Center for Diabetes Research (DZD), Neuherberg, Germany.ORCID 0000-0002-8462-3832
Sabine M HölterGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0003-4878-5241
Paul T PflugerResearch Unit Neurobiology of Diabetes, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0002-8118-7588
Helmholtz Zentrum München · DEUniversity Children's Hospital Tübingen · DEDeutsches Diabetes-Zentrum e.V. · DEGerman Center for Neurodegenerative Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDusp8 is the first GWAS-identified gene that is predominantly expressed in the brain and has previously been linked with the development of diabetes type 2 in humans. In this study, we unravel how Dusp8 is involved in the regulation of sucrose reward behavior.

methodsFemale, chow-fed global Dusp8 WT and KO mice were tested in an observer-independent IntelliCage setup for self-administrative sucrose consumption and preference followed by a progressive ratio task with restricted sucrose access to monitor seeking and motivation behavior. Sixty-three human carriers of the major C and minor T allele of DUSP8 SNP rs2334499 were tested for their perception of food cues by collecting a rating score for sweet versus savory high caloric food.

resultsDusp8 KO mice showed a comparable preference for sucrose, but consumed more sucrose compared to WT mice. In a progressive ratio task, Dusp8 KO females switched to a "trial and error" strategy to find sucrose while control Dusp8 WT mice kept their previously established seeking pattern. Nonetheless, the overall motivation to consume sucrose, and the levels of dopaminergic neurons in the brain areas NAcc and VTA were comparable between genotypes. Diabetes-risk allele carriers of DUSP8 SNP rs2334499 preferred sweet high caloric food compared to the major allele carriers, rating scores for savory food remained comparable between groups.

conclusionOur data suggest a novel role for Dusp8 in the perception of sweet high caloric food as well as in the control of sucrose consumption and foraging in mice and humans.

Indexed as

Diabetes Mellitus, Type 2SucroseAnimalsDual-Specificity PhosphatasesFeeding BehaviorFemaleHumansMiceMotivationRewardDual-Specificity PhosphatasesDUSP8 protein, humanDUSP8 protein, mouseSucrosedopamineDusp8MAP kinasesucrose reward

Identifiers

PMID33131190
PMCPMC7821601
OpenAlexW3097625555

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.