Evidence map›Paper›PMID 26872351›Full record

ArticlePloS one2016

Age Related Bioenergetics Profiles in Isolated Rat Cardiomyocytes Using Extracellular Flux Analyses.

Kennedy S Mdaki, Tricia D Larsen, Lucinda J Weaver, Michelle L Baack

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-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

26 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  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

4 authors at 2 institutions in 1 country.

Kennedy S MdakiChildren's Health Research Center, Sanford Research, Sioux Falls, SD, United States of America.
Tricia D LarsenChildren's Health Research Center, Sanford Research, Sioux Falls, SD, United States of America.
Lucinda J WeaverSanford School of Medicine-University of South Dakota, Sioux Falls, SD, United States of America.
Michelle L BaackChildren's Health Research Center, Sanford Research, Sioux Falls, SD, United States of America.
Sanford Research · USUniversity of South Dakota · US

Funding

The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI SAVINOV, ALEXEI YURIEVITCH · 2012 to 2020
$20.8M
Lipotoxic Effects of Maternal Diabetes and High Fat Diet on the Developing HeartK08HD078504 · NICHD · SANFORD RESEARCH/USD · PI BAACK, MICHELLE LEIGH · 2014 to 2018
$599k
NICHD NIH HHS K08 HD078504NICHD NIH HHS K08HD078504NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20GM103548
6 · The paper itself

Abstract

Mitochondrial dysfunction is increasingly recognized and studied as a mediator of heart disease. Extracellular flux analysis (XF) has emerged as a powerful tool to investigate cellular bioenergetics in the context of cardiac health and disease, however its use and interpretation requires improved understanding of the normal metabolic differences in cardiomyocytes (CM) at various stages of maturation. This study standardized XF analyses methods (mitochondrial stress test, glycolytic stress test and palmitate oxidation test) and established age related differences in bioenergetics profiles of healthy CMs at newborn (NB1), weaning (3WK), adult (10WK) and aged (12-18MO) time points. Findings show that immature CMs demonstrate a more robust and sustained glycolytic capacity and a relative inability to oxidize fatty acids when compared to older CMs. The study also highlights the need to recognize the contribution of CO2 from the Krebs cycle as well as lactate from anaerobic glycolysis to the proton production rate before interpreting glycolytic capacity in CMs. Overall, this study demonstrates that caution should be taken to assure that translatable developmental time points are used to investigate mitochondrial dysfunction as a cause of cardiac disease. Specifically, XF analysis of newborn CMs should be reserved to study fetal/neonatal disease and older CMs (≥10 weeks) should be used to investigate adult disease pathogenesis. Knowledge gained will aid in improved investigation of developmentally programmed heart disease and stress the importance of discerning maturational differences in bioenergetics when developing mitochondrial targeted preventative and therapeutic strategies for cardiac disease.

Indexed as

Metabolic Flux AnalysisOxidative PhosphorylationAgingAnimalsAnimals, NewbornCarbon DioxideFatty AcidsFemaleGlycolysisLactic AcidMitochondriaMyocytes, CardiacPrimary Cell CultureRatsRats, Sprague-DawleyWeaningCarbon DioxideFatty AcidsLactic Acid

Identifiers

PMID26872351
PMCPMC4752341
OpenAlexW2259843633

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.