Evidence map›Paper›PMID 28338413›Full record

ArticleTissue engineering. Part C, Methods2017

Human, Tissue-Engineered, Skeletal Muscle Myobundles to Measure Oxygen Uptake and Assess Mitochondrial Toxicity.

Brittany N J Davis, Jeffrey W Santoso, Michaela J Walker, Cindy S Cheng, Timothy R Koves, William E Kraus, George A Truskey

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Neuromuscular disease modeling on a chip.Disease models & mechanisms · 2020
    Review
  9. Tissue-Engineered Human Myobundle System as a Platform for Evaluation of Skeletal Muscle Injury Biomarkers.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Human Microphysiological Systems and Organoids asFrontiers in public health · 2018
    Review
  16. 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

7 authors at 1 institution in 1 country.

Brittany N J Davis1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Jeffrey W Santoso1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Michaela J Walker1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Cindy S Cheng1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Timothy R Koves2 Duke Molecular Physiology Institute, Duke University School of Medicine , Durham, North Carolina.
William E Kraus1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
George A Truskey1 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Duke University · US

Funding

Interaction of Subchondral Bone and Articular Cartilage System with Skeletal MuscleUH3TR000505 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2014 to 2016
$3.6M
Circulatory system and integrated muscle tissue for drug and tissue toxicityUH2TR000505 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2012 to 2013
$2.1M
NCATS NIH HHS UH2 TR000505NCATS NIH HHS UH3 TR000505
6 · The paper itself

Abstract

Mitochondrial dysfunction is responsible for the toxicity of a number of drugs. Current isolated mitochondria or cellular monoculture mitochondrial respiration measurement systems lack physiological relevance. Using a tissue engineering rather than cell- or mitochondria-based approach enables a more physiologically relevant detection of drug-induced mitochondrial impairment. To probe oxygen consumption and mitochondrial health, we assayed the bioenergetic profile of engineered three-dimensional human skeletal muscle myobundles derived from primary myoblasts. Through experimental and computational techniques, we did not find external or internal oxygen transport limiting the engineered myobundles in the commercial O2k system to measure oxygen consumption. In response to the complex I inhibitor rotenone, myobundle basal respiration decreased dose dependently with an IC

Indexed as

Models, BiologicalComputer SimulationElectron Transport Complex IHumansMitochondria, MuscleMuscle Fibers, SkeletalOxygenOxygen ConsumptionRotenoneTissue EngineeringElectron Transport Complex IOxygenRotenonebioenergeticsdrug testinghuman skeletal musclemitochondrial toxicityoxygen consumption ratetissue engineering

Identifiers

PMID28338413
PMCPMC5397214
OpenAlexW2600933586

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.