Evidence map›Paper›PMID 20856881›Full record

ArticlePloS one2010

Complex I-associated hydrogen peroxide production is decreased and electron transport chain enzyme activities are altered in n-3 enriched fat-1 mice.

Kevork Hagopian, Kristina L Weber, Darren T Hwee, Alison L Van Eenennaam, Guillermo López-Lluch, José M Villalba, Isabel Burón, Plácido Navas, J Bruce German, Steven M Watkins and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. CytochromeNPJ aging and mechanisms of disease · 2016
    Article
  13. Dietary Fatty Acids and Temperature Modulate Mitochondrial Function and Longevity in Drosophila.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    Article
  14. Review
  15. The Influence of Dietary Fat Source on Life Span in Calorie Restricted Mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    Article
  16. Article
  17. Dietary fat, fatty acid saturation and mitochondrial bioenergetics.Journal of bioenergetics and biomembranes · 2014
    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

14 authors at 4 institutions in 2 countries.

Kevork HagopianVM Molecular Biosciences, University of California Davis, Davis, California, United States of America.
Kristina L Weber
Darren T Hwee
Alison L Van Eenennaam
Guillermo López-Lluch
José M Villalba
Isabel Burón
Plácido Navas
J Bruce German
Steven M Watkins
Yana Chen
Alfreda Wei
Roger B McDonald
Jon J Ramsey
University of California, Davis · USUniversity of Córdoba · ESCentro Andaluz de Biología del Desarrollo · ESConsejo Superior de Investigaciones Científicas · ES

Funding

Alterations in membrane composition and function eith calorie restrictionR01AG028125 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RAMSEY, JON J. · 2007 to 2011
$1.4M
NIA NIH HHS R01 AG-028125NIA NIH HHS R01 AG028125
6 · The paper itself

Abstract

The polyunsaturated nature of n-3 fatty acids makes them prone to oxidative damage. However, it is not clear if n-3 fatty acids are simply a passive site for oxidative attack or if they also modulate mitochondrial reactive oxygen species (ROS) production. The present study used fat-1 transgenic mice, that are capable of synthesizing n-3 fatty acids, to investigate the influence of increases in n-3 fatty acids and resultant decreases in the n-6:n-3 ratio on liver mitochondrial H(2)O(2) production and electron transport chain (ETC) activity. There was an increase in n-3 fatty acids and a decrease in the n-6:n-3 ratio in liver mitochondria from the fat-1 compared to control mice. This change was largely due to alterations in the fatty acid composition of phosphatidylcholine and phosphatidylethanolamine, with only a small percentage of fatty acids in cardiolipin being altered in the fat-1 animals. The lipid changes in the fat-1 mice were associated with a decrease (p<0.05) in the activity of ETC complex I and increases (p<0.05) in the activities of complexes III and IV. Mitochondrial H(2)O(2) production with either succinate or succinate/glutamate/malate substrates was also decreased (p<0.05) in the fat-1 mice. This change in H(2)O(2) production was due to a decrease in ROS production from ETC complex I in the fat-1 animals. These results indicate that the fatty acid changes in fat-1 liver mitochondria may at least partially oppose oxidative stress by limiting ROS production from ETC complex I.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsElectron TransportElectron Transport Complex IFatty Acid DesaturasesFatty Acids, Omega-3Fatty Acids, Omega-6Hydrogen PeroxideLiverMaleMiceMice, TransgenicMitochondriaCaenorhabditis elegans ProteinsElectron Transport Complex Ifat-1 protein, C elegansFatty Acid DesaturasesFatty Acids, Omega-3Fatty Acids, Omega-6Hydrogen Peroxide

Identifiers

PMID20856881
PMCPMC2938348
OpenAlexW2112638909

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.