Evidence map›Paper›PMID 18387886›Full record

ArticleJournal of lipid research2008

Bioinformatic profiling of the transcriptional response of adult rat cardiomyocytes to distinct fatty acids.

Joseph B Lockridge, Mary L Sailors, David J Durgan, Oluwaseun Egbejimi, William J Jeong, Molly S Bray, William C Stanley, Martin E Young

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  6. Destabilization of β Cell FIT2 by saturated fatty acids alter lipid droplet numbers and contribute to ER stress and diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Plin5 Bidirectionally Regulates Lipid Metabolism in Oxidative Tissues.Oxidative medicine and cellular longevity · 2022
    Review
  8. Review
  9. Article
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  16. Review
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  18. Decreased long-chain fatty acid oxidation impairs postischemic recovery of the insulin-resistant rat heart.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Joseph B LockridgeUniversity of Texas Health Science Center at Houston, Brown Foundation Institute of Molecular Medicine, Houston TX, USA.
Mary L Sailors
David J Durgan
Oluwaseun Egbejimi
William J Jeong
Molly S Bray
William C Stanley
Martin E Young
United States Department of Agriculture · USBaylor College of Medicine · USBrown Foundation · USChildren's Nutrition Research Center at Baylor College of Medicine · USUniversity of Maryland, Baltimore · US

Funding

Role of the Molecular Circadian Clock within the HeartR01HL074259 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YOUNG, MARTIN E · 2004 to 2012
$3.1M
NHLBI NIH HHS HL-074259NHLBI NIH HHS R01 HL074259
6 · The paper itself

Abstract

Diabetes mellitus, obesity, and dyslipidemia increase risk for cardiovascular disease, and expose the heart to high plasma fatty acid (FA) levels. Recent studies suggest that distinct FA species are cardiotoxic (e.g., palmitate), while others are cardioprotective (e.g., oleate), although the molecular mechanisms mediating these observations are unclear. The purpose of the present study was to investigate the differential effects of distinct FA species (varying carbon length and degree of saturation) on adult rat cardiomyocyte (ARC) gene expression. ARCs were initially challenged with 0.4 mM octanoate (8:0), palmitate (16:0), stearate (18:0), oleate (18:1), or linoleate (18:2) for 24 h. Microarray analysis revealed differential regulation of gene expression by the distinct FAs; the order regarding the number of genes whose expression was influenced by a specific FA was octanoate (1,188) > stearate (740) > palmitate (590) > oleate (83) > linoleate (65). In general, cardioprotective FAs (e.g., oleate) increased expression of genes promoting FA oxidation to a greater extent than cardiotoxic FAs (e.g., palmitate), whereas the latter induced markers of endoplasmic reticulum and oxidative stress. Subsequent RT-PCR analysis revealed distinct time- and concentration-dependent effects of these FA species, in a gene-specific manner. For example, stearate- and palmitate-mediated ucp3 induction tended to be transient (i.e., initial high induction, followed by subsequent repression), whereas oleate-mediated induction was sustained. These findings may provide insight into why diets high in unsaturated FAs (e.g., oleate) are cardioprotective, whereas diets rich in saturated FAs (e.g., palmitate) are not.

Indexed as

AgingAnimalsComputational BiologyFatty AcidsGene Expression ProfilingGene Expression RegulationGenomeMaleMyocytes, CardiacRatsRats, WistarTime FactorsTranscription, GeneticFatty Acids

Identifiers

PMID18387886
PMCPMC2431101
OpenAlexW2168505148

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.