Evidence map›Paper›PMID 28327588›Full record

ArticleNature communications2017

Pharmacological inhibition of adipose triglyceride lipase corrects high-fat diet-induced insulin resistance and hepatosteatosis in mice.

Martina Schweiger, Matthias Romauch, Renate Schreiber, Gernot F Grabner, Sabrina Hütter, Petra Kotzbeck, Pia Benedikt, Thomas O Eichmann, Sohsuke Yamada, Oskar Knittelfelder and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. 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 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
13.8field-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

119 citing papers in PubMed, 206 citations in OpenAlex.

  1. Article
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  7. Copper Import via CTR1 Supports the β3-Adrenergic Thermogenic Program.bioRxiv : the preprint server for biology · 2026
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59 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Martina SchweigerInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.ORCID 0000-0002-3419-1007
Matthias RomauchInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Renate SchreiberInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Gernot F GrabnerInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Sabrina HütterInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Petra KotzbeckInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Pia BenediktInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Thomas O EichmannInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Sohsuke YamadaInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Oskar KnittelfelderInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Clemens DiwokyInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Carina DolerInstitute of Organic Chemistry, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria.
Nicole MayerInstitute of Organic Chemistry, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria.
Werner De CeccoInstitute of Chemistry, University of Graz, Heinrichstrasse 28, 8010 Graz, Austria.
Rolf BreinbauerInstitute of Organic Chemistry, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria.ORCID 0000-0001-6009-7359
Robert ZimmermannInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
Rudolf ZechnerInstitute of Molecular Biosciences, University of Graz, Heinrichstrasse 31, 8010 Graz, Austria.
University of Graz · ATGraz University of Technology · AT

Funding

Austrian Science Fund FWF P 28286European Research Council 340896
6 · The paper itself

Abstract

Elevated circulating fatty acids (FAs) contribute to the development of obesity-associated metabolic complications such as insulin resistance (IR) and non-alcoholic fatty liver disease (NAFLD). Hence, reducing adipose tissue lipolysis to diminish the mobilization of FAs and lower their respective plasma concentrations represents a potential treatment strategy to counteract obesity-associated disorders. Here we show that specific inhibition of adipose triglyceride lipase (Atgl) with the chemical inhibitor, Atglistatin, effectively reduces adipose tissue lipolysis, weight gain, IR and NAFLD in mice fed a high-fat diet. Importantly, even long-term treatment does not lead to lipid accumulation in ectopic tissues such as the skeletal muscle or heart. Thus, the severe cardiac steatosis and cardiomyopathy that is observed in genetic models of Atgl deficiency does not occur in Atglistatin-treated mice. Our data validate the pharmacological inhibition of Atgl as a potentially powerful therapeutic strategy to treat obesity and associated metabolic disorders.

Indexed as

Insulin ResistanceAdipose Tissue, WhiteAnimalsBody WeightDiet, High-FatFatty LiverFeeding BehaviorGlucoseHomeostasisHumansLipaseLipolysisMaleMice, Inbred C57BLObesityPhenylurea CompoundsatglistatinGlucoseLipasePhenylurea Compounds

Identifiers

PMID28327588
PMCPMC5364409
OpenAlexW2601642277

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.