Evidence map›Paper›PMID 28065827›Full record

ArticleCell metabolism2017

Gastric Bypass Surgery Recruits a Gut PPAR-α-Striatal D1R Pathway to Reduce Fat Appetite in Obese Rats.

Mohammed K Hankir, Florian Seyfried, Constantin A Hintschich, Thi-Ai Diep, Karen Kleberg, Mathias Kranz, Winnie Deuther-Conrad, Luis A Tellez, Michael Rullmann, Marianne Patt and 8 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Cell metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
20.6field-weighted citation impact, top 1% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

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  10. Novel neural pathways targeted by GLP-1R agonists and bariatric surgery.Pflugers Archiv : European journal of physiology · 2025
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 3 countries.

Mohammed K HankirIntegrated Research and Treatment Centre for Adiposity Diseases, Department of Medicine, Universität Leipzig, Liebigstraße 21, 04103 Leipzig, Germany.
Florian SeyfriedDepartment of General and Visceral, Vascular, and Paediatric Surgery, University of Würzburg, 97070 Würzburg, Germany.
Constantin A HintschichIntegrated Research and Treatment Centre for Adiposity Diseases, Department of Medicine, Universität Leipzig, Liebigstraße 21, 04103 Leipzig, Germany.
Thi-Ai DiepNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B Building 18.5, 2200 Copenhagen, Denmark.
Karen KlebergDepartment of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 1165 Copenhagen, Denmark.
Mathias KranzHelmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Permoserstraße 15, 04318 Leipzig, Germany.
Winnie Deuther-ConradHelmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Permoserstraße 15, 04318 Leipzig, Germany.
Luis A TellezJohn B. Pierce Laboratory and Departments of Psychiatry and Physiology, Yale University, New Haven, CT 06519, USA.
Michael RullmannDepartment of Nuclear Medicine, Universität Leipzig, Liebigstraße 18, 04109 Leipzig, Germany.
Marianne PattDepartment of Nuclear Medicine, Universität Leipzig, Liebigstraße 18, 04109 Leipzig, Germany.
Jens TeichertRudolf Boehm Institute of Pharmacology and Toxicology, Clinical Pharmacology, Universität Leipzig, Härtelstraße 16-18, 04107 Leipzig, Germany.
Swen HesseIntegrated Research and Treatment Centre for Adiposity Diseases, Department of Medicine, Universität Leipzig, Liebigstraße 21, 04103 Leipzig, Germany; Department of Nuclear Medicine, Universität Leipzig, Liebigstraße 18, 04109 Leipzig, Germany.
Osama SabriIntegrated Research and Treatment Centre for Adiposity Diseases, Department of Medicine, Universität Leipzig, Liebigstraße 21, 04103 Leipzig, Germany; Department of Nuclear Medicine, Universität Leipzig, Liebigstraße 18, 04109 Leipzig, Germany.
Peter BrustHelmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Permoserstraße 15, 04318 Leipzig, Germany.
Harald S HansenDepartment of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 1165 Copenhagen, Denmark.
Ivan E de AraujoJohn B. Pierce Laboratory and Departments of Psychiatry and Physiology, Yale University, New Haven, CT 06519, USA.
Ute KrügelRudolf Boehm Institute of Pharmacology and Toxicology, Universität Leipzig, Härtelstraße 16-18, 04107 Leipzig, Germany. Electronic address: ute.kruegel@medizin.uni-leipzig.de.
Wiebke K FenskeIntegrated Research and Treatment Centre for Adiposity Diseases, Department of Medicine, Universität Leipzig, Liebigstraße 21, 04103 Leipzig, Germany. Electronic address: wiebkekristin.fenske@medizin.uni-leipzig.de.
IFB Adiposity Diseases · DELeipzig University · DEHelmholtz-Zentrum Dresden-Rossendorf · DEUniversity of Copenhagen · DKYale University · USUniversity of Würzburg · DE

Funding

Neural circuitry of sweet tasteR01DC014859 · NIDCD · JOHN B. PIERCE LABORATORY, INC. · PI DE ARAUJO, IVAN E · 2015 to 2019
$1.5M
NIDCD NIH HHS R01 DC014859
6 · The paper itself

Abstract

Bariatric surgery remains the single most effective long-term treatment modality for morbid obesity, achieved mainly by lowering caloric intake through as yet ill-defined mechanisms. Here we show in rats that Roux-en-Y gastric bypass (RYGB)-like rerouting of ingested fat mobilizes lower small intestine production of the fat-satiety molecule oleoylethanolamide (OEA). This was associated with vagus nerve-driven increases in dorsal striatal dopamine release. We also demonstrate that RYGB upregulates striatal dopamine 1 receptor (D1R) expression specifically under high-fat diet feeding conditions. Mechanistically, interfering with local OEA, vagal, and dorsal striatal D1R signaling negated the beneficial effects of RYGB on fat intake and preferences. These findings delineate a molecular/systems pathway through which bariatric surgery improves feeding behavior and may aid in the development of novel weight loss strategies that similarly modify brain reward circuits compromised in obesity.

Indexed as

Gastric BypassSignal TransductionAdministration, OralAnimalsAppetiteBody WeightDietary FatsDiet, High-FatDopamineEndocannabinoidsFeeding BehaviorFood PreferencesGastrointestinal TractIntestine, SmallMaleMice, ObeseDietary FatsDopamineEndocannabinoidsOleic AcidsoleoylethanolamidePPAR alphaReceptors, Dopamine D1[11C] SCH 23390altered nutrient preferenceD1R signalingdopamine systemfat appetitegastric bypass surgeryOEAPPAR-alpha

Identifiers

PMID28065827
OpenAlexW2570089409

What OpenQuestion holds

Textmetadata
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.