Evidence map›Paper›PMID 23867907›Full record

ArticleBiochimica et biophysica acta2013

Cardiac oxidative stress in a mouse model of neutral lipid storage disease.

Astrid Schrammel, Marion Mussbacher, Sarah Winkler, Guenter Haemmerle, Heike Stessel, Gerald Wölkart, Rudolf Zechner, Bernd Mayer

Open access · hybridAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Effect of Crocetin on Basal Lipolysis in 3T3-L1 Adipocytes.Antioxidants (Basel, Switzerland) · 2023
    Article
  6. Article
  7. Frontiers in veterinary science · 2022
    Article
  8. Lipotoxicity: a driver of heart failure with preserved ejection fraction?Clinical science (London, England : 1979) · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Cell Death and Heart Failure in Obesity: Role of Uncoupling Proteins.Oxidative medicine and cellular longevity · 2016
    Review
  17. 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

8 authors at 1 institution in 1 country.

Astrid SchrammelDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: astrid.schrammel-gorren@uni-graz.at.
Marion MussbacherDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: marion.mussbacher@uni-graz.at.
Sarah WinklerDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: sarah.winkler@uni-graz.at.
Guenter HaemmerleDepartment of Molecular Biosciences, University of Graz, Heinrichstraße 31, 8010 Graz, Austria. Electronic address: guenter.haemmerle@uni-graz.at.
Heike StesselDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: heike.stessel@uni-graz.at.
Gerald WölkartDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: gerald.woelkart@uni-graz.at.
Rudolf ZechnerDepartment of Molecular Biosciences, University of Graz, Heinrichstraße 31, 8010 Graz, Austria. Electronic address: rudolf.zechner@uni-graz.at.
Bernd MayerDepartment of Pharmacology and Toxicology, Institute of Pharmaceutical Sciences, University of Graz, Universitätsplatz 2, 8010 Graz, Austria. Electronic address: mayer@uni-graz.at.
University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac oxidative stress has been implicated in the pathogenesis of hypertrophy, cardiomyopathy and heart failure. Systemic deletion of the gene encoding adipose triglyceride lipase (ATGL), the enzyme that catalyzes the rate-limiting step of triglyceride lipolysis, results in a phenotype characterized by severe steatotic cardiac dysfunction. The objective of the present study was to investigate a potential role of oxidative stress in cardiac ATGL deficiency. Hearts of mice with global ATGL knockout were compared to those of mice with cardiomyocyte-restricted overexpression of ATGL and to those of wildtype littermates. Our results demonstrate that oxidative stress, measured as lucigenin chemiluminescence, was increased ~6-fold in ATGL-deficient hearts. In parallel, cytosolic NADPH oxidase subunits p67phox and p47phox were upregulated 4-5-fold at the protein level. Moreover, a prominent upregulation of different inflammatory markers (tumor necrosis factor α, monocyte chemotactant protein-1, interleukin 6, and galectin-3) was observed in those hearts. Both the oxidative and inflammatory responses were abolished upon cardiomyocyte-restricted overexpression of ATGL. Investigating the effect of oxidative and inflammatory stress on nitric oxide/cGMP signal transduction we observed a ~2.5-fold upregulation of soluble guanylate cyclase activity and a ~2-fold increase in cardiac tetrahydrobiopterin levels. Systemic treatment of ATGL-deficient mice with the superoxide dismutase mimetic Mn(III)tetrakis (4-benzoic acid) porphyrin did not ameliorate but rather aggravated cardiac oxidative stress. Our data suggest that oxidative and inflammatory stress seems involved in lipotoxic heart disease. Upregulation of soluble guanylate cyclase and cardiac tetrahydrobiopterin might be regarded as counterregulatory mechanisms in cardiac ATGL deficiency.

Indexed as

AcyltransferasesAnimalsBlotting, WesternDisease Models, AnimalIchthyosiform Erythroderma, CongenitalLipaseLipid Metabolism, Inborn ErrorsMiceMice, Mutant StrainsModels, BiologicalMuscular DiseasesMyocardiumOxidative StressAcyltransferasesLipasePNPLA2 protein, mouse2,2-diethyl-1-nitroso-oxyhydrazineadipose triglyceride lipaseAdipose triglyceride lipaseadipose triglyceride lipase knockoutATGLATGL(−/−)BH(2)BH(4)Cardiac hypertrophyDAGDEA/NOdiacylglyceroldihydrobiopterin, [2-amino-6-(1,2-dihydroxypropyl)-7,8-dihydro-1H-pteridin-4-one]endothelial nitric oxide synthaseeNOSFFAfree fatty acidgalectin-3GAPDHglyceraldehyde-3-phosphate dehydrogenaseIL-6inducible nitric oxide synthaseInflammationiNOSinterleukin 6Mac-2MCP-1Mn(III)tetrakis (4-benzoic acid) porphyrin chlorideMnTBAPmonocyte chemotactic protein-1NADPHNADPH oxidaseneuronal nitric oxide synthasenicotinamide adenine dinucleotide phosphatenitric oxidenNOSNONOXONOO(−)Oxidative stressPBSperoxisome proliferator receptor αperoxynitritephosphate-buffered salinephosphorylated vasodilator-stimulated phosphoproteinPKCPPARαprotein kinase CpVASP(s)GCSOD(soluble) guanylate cyclasesuperoxide dismutasetetrahydrobiopterin, [(6R)-2-amino-6-[(1R,2S)-1,2-dihydroxypropyl]-5,6,7,8-tetrahydropteridin-4(1H)-one]TGTNFαtriacylglyceroltumor necrosis factor αvasodilator-stimulated phosphoproteinVASP

Identifiers

PMID23867907
PMCPMC3795454
OpenAlexW2068251843

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.