Evidence map›Paper›PMID 23825227›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Decreased long-chain fatty acid oxidation impairs postischemic recovery of the insulin-resistant rat heart.

Romain Harmancey, Hernan G Vasquez, Patrick H Guthrie, Heinrich Taegtmeyer

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Insulin signaling in the heart.American journal of physiology. Endocrinology and metabolism · 2021
    Review
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  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Skeletal muscle mitoflashes, pH, and the role of uncoupling protein-3.Archives of biochemistry and biophysics · 2019
    Article
  17. Article
  18. Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Romain Harmancey1University of Texas Medical School at Houston, 6431 Fannin, MSB 1.246, Houston, TX 77030, USA. heinrich.taegtmeyer@uth.tmc.edu.
Hernan G Vasquez
Patrick H Guthrie
Heinrich Taegtmeyer
The University of Texas Health Science Center at Houston · US

Funding

Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
SWITCHING OF METABOLIC GENES IN UNLOADED HEARTR01HL061483 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TAEGTMEYER, HEINRICH · 1999 to 2021
$6.2M
NHLBI NIH HHS R01 HL061483NHLBI NIH HHS R01-HL-061483NIDDK NIH HHS P30 DK-079638NIDDK NIH HHS P30 DK079638
6 · The paper itself

Abstract

Diabetic patients with acute myocardial infarction are more likely to die than nondiabetic patients. In the present study we examined the effect of insulin resistance on myocardial ischemia tolerance. Hearts of rats, rendered insulin resistant by high-sucrose feeding, were subjected to ischemia/reperfusion ex vivo. Cardiac power of control hearts from chow-fed rats recovered to 93%, while insulin-resistant hearts recovered only to 80% (P<0.001 vs. control). Unexpectedly, impaired contractile recovery did not result from an impairment of glucose oxidation (576±36 vs. 593±42 nmol/min/g dry weight; not significant), but from a failure to increase and to sustain oxidation of the long-chain fatty acid oleate on reperfusion (1878±56 vs. 2070±67 nmol/min/g dry weight; P<0.05). This phenomenon was due to a reduced ability to transport oleate into mitochondria and associated with a 38-58% decrease in the mitochondrial uncoupling protein 3 (UCP3) levels. Contractile function was rescued by replacing oleate with a medium-chain fatty acid or by restoring UCP3 levels with 24 h of food withdrawal. Lastly, the knockdown of UCP3 in rat L6 myocytes also decreased oleate oxidation by 13-18% following ischemia. Together the results expose UCP3 as a critical regulator of long-chain fatty acid oxidation in the stressed heart postischemia and identify octanoate as an intervention by which myocardial metabolism can be manipulated to improve function of the insulin-resistant heart.

Indexed as

Animal FeedAnimalsCaprylatesDietDietary CarbohydratesFatty AcidsGene Expression RegulationGlucoseInsulinInsulin ResistanceIon ChannelsMaleMitochondrial ProteinsOxidation-ReductionProto-Oncogene Proteins c-aktRatsCaprylatesDietary CarbohydratesFatty AcidsGlucoseInsulinIon ChannelsMitochondrial Proteinsoctanoic acidProto-Oncogene Proteins c-aktSucroseUcp3 protein, ratUncoupling Protein 3cardiac functionhigh-sucrose dietmyocardial metabolismtype 2 diabetesuncoupling proteins

Identifiers

PMID23825227
PMCPMC4046182
OpenAlexW2160973808

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.