Evidence map›Paper›PMID 28702329›Full record

ArticleMolecular metabolism2017

Metformin causes a futile intestinal-hepatic cycle which increases energy expenditure and slows down development of a type 2 diabetes-like state.

Philipp Schommers, Anna Thurau, Insa Bultmann-Mellin, Maria Guschlbauer, Andreas R Klatt, Jan Rozman, Martin Klingenspor, Martin Hrabe de Angelis, Jens Alber, Dirk Gründemann and 2 more

Open access · goldFull text read
In one paragraph

Article in Molecular metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  5. Review
  6. The Gut Microbiota-Related Antihyperglycemic Effect of Metformin.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Metabolic Action of Metformin.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  15. Article
  16. Review
  17. Metformin action in the gut-insight provided by [Diabetology international · 2022
    Article
  18. Article
  19. Article
  20. 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

12 authors at 6 institutions in 1 country.

Philipp SchommersInstitute of Vegetative Physiology, Medical Faculty, University of Köln, 50931 Köln, Germany.
Anna ThurauInstitute of Vegetative Physiology, Medical Faculty, University of Köln, 50931 Köln, Germany.
Insa Bultmann-MellinCenter for Experimental Medicine, Medical Faculty, University Hospital Cologne, 50931 Köln, Germany.
Maria GuschlbauerCenter for Experimental Medicine, Medical Faculty, University Hospital Cologne, 50931 Köln, Germany.
Andreas R KlattInstitute for Clinical Chemistry, Medical Faculty, University Hospital Cologne, 50931 Köln, Germany.
Jan RozmanGerman Mouse Clinic, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
Martin KlingensporGerman Mouse Clinic, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
Martin Hrabe de AngelisGerman Mouse Clinic, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
Jens AlberMax-Planck Institute for Metabolism Research, 50931 Köln, Germany.
Dirk GründemannDepartment of Pharmacology, Medical Faculty, University of Köln, 50931 Köln, Germany.
Anja Sterner-KockCenter for Experimental Medicine, Medical Faculty, University Hospital Cologne, 50931 Köln, Germany.
Rudolf J WiesnerInstitute of Vegetative Physiology, Medical Faculty, University of Köln, 50931 Köln, Germany.
University Hospital Cologne · DEUniversity of Cologne · DEHeinrich Heine University Düsseldorf · DECologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEFresenius (Germany) · DEMax Planck Institute for Metabolism Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMetformin, the first line drug for treatment of type 2 diabetes, suppresses hepatic gluconeogenesis and reduces body weight in patients, the latter by an unknown mechanism.

methodsMice on a high fat diet were continuously fed metformin in a therapeutically relevant dose, mimicking a retarded formulation.

resultsFeeding metformin in pharmacologically relevant doses to mice on a high fat diet normalized HbA1c levels and ameliorated glucose tolerance, as expected, but also considerably slowed down weight gain. This was due to increased energy expenditure, since food intake was unchanged and locomotor activity was even decreased. Metformin caused lactate accumulation in the intestinal wall and in portal venous blood but not in peripheral blood or the liver. Increased conversion of glucose-1-

conclusionsThe reported glucose-lactate-glucose cycle is a highly energy consuming process, explaining the beneficial effects of metformin given continuously on the development of a type 2 diabetic-like state in our mice.

Indexed as

Energy MetabolismAnimalsDiabetes Mellitus, Type 2Diet, High-FatGlucoseHypoglycemic AgentsIntestinal MucosaIntestinesLactic AcidLiverMaleMetforminMiceMice, Inbred C57BLGlucoseHypoglycemic AgentsLactic AcidMetforminFutile cycleMetforminMitochondriaSplanchnic bed

Identifiers

PMID28702329
PMCPMC5485244
OpenAlexW2610525859

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.