Evidence map›Paper›PMID 12730300›Full record

ArticleJournal of lipid research2003

Isomer-specific regulation of metabolism and PPARgamma signaling by CLA in human preadipocytes.

J Mark Brown, Maria Sandberg Boysen, Søren Skov Jensen, Ron F Morrison, Jayne Storkson, Renee Lea-Currie, Michael Pariza, Susanne Mandrup, Michael K McIntosh

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

70 citing papers in PubMed, 222 citations in OpenAlex.

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  18. Bioconversion of conjugated linoleic acid byFood science and biotechnology · 2017
    Article
  19. Article
  20. Nutrigenomics and Beef Quality: A Review about Lipogenesis.International journal of molecular sciences · 2016
    Review

10 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

J Mark BrownDepartment of Nutrition, University of North Carolina at Greensboro, Greensboro, NC 27402-6170, USA.
Maria Sandberg Boysen
Søren Skov Jensen
Ron F Morrison
Jayne Storkson
Renee Lea-Currie
Michael Pariza
Susanne Mandrup
Michael K McIntosh
University of North Carolina at Greensboro · USUniversity of Southern Denmark · DKUniversity of Wisconsin–Madison · USZen Bio (United States) · US

Funding

Antiobesity Mechanism of CLA Isomer in Human AdipocytesR01DK063070 · NIDDK · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI MCINTOSH, MICHAEL K · 2002 to 2011
$2.7M
CLA Reduces Adipogenesis In Human PreadipocytesR15DK059289 · NIDDK · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI MCINTOSH, MICHAEL K · 2001 to 2001
$129k
NIDDK NIH HHS DK 59289-01NIDDK NIH HHS DK 630289NIDDK NIH HHS R01 DK063070
6 · The paper itself

Abstract

Trans-10,cis-12 conjugated linoleic acid (CLA) has previously been shown to be the CLA isomer responsible for CLA-induced reductions in body fat in animal models, and we have shown that this isomer, but not the cis-9,trans-11 CLA isomer, specifically decreased triglyceride (TG) accumulation in primary human adipocytes in vitro. Here we investigated the mechanism behind the isomer-specific, CLA-mediated reduction in TG accumulation in differentiating human preadipocytes. Trans-10,cis-12 CLA decreased insulin-stimulated glucose uptake and oxidation, and reduced insulin-dependent glucose transporter 4 gene expression. Furthermore, trans-10,cis-12 CLA reduced oleic acid uptake and oxidation when compared with all other treatments. In parallel to CLA's effects on metabolism, trans-10,cis-12 CLA decreased, whereas cis-9,trans-11 CLA increased, the expression of peroxisome proliferator-activated receptor gamma (PPARgamma) and several of its downstream target genes when compared with vehicle controls. Transient transfections demonstrated that both CLA isomers antagonized ligand-dependent activation of PPARgamma. Collectively, trans-10,cis-12, but not cis-9, trans-11, CLA decreased glucose and lipid uptake and oxidation and preadipocyte differentiation by altering preadipocyte gene transcription in a manner that appeared to be due, in part, to decreased PPARgamma expression.

Indexed as

3T3-L1 CellsAdipocytesAdipose TissueAnimalsAntimetabolitesCarbon DioxideCell DifferentiationCells, CulturedChromatography, GasDeoxyglucoseDose-Response Relationship, DrugFatty AcidsGene Expression RegulationGlucoseHumansImmunoblottingAntimetabolitesCarbon DioxideDeoxyglucoseFatty AcidsGlucoseLinoleic Acids, ConjugatedOleic AcidOligonucleotidesOxygenPhospholipidsProtein IsoformsReceptors, Cytoplasmic and NuclearRNATranscription FactorsTriglyceridesWater

Identifiers

PMID12730300
PMCPMC1351019
OpenAlexW2127211761

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.