Evidence map›Paper›PMID 24421861›Full record

ArticleDrug discovery today. Disease models2008

Models of muscle contraction and energetics.

Nicola Lai, L Bruce Gladden, Pierre G Carlier, Marco E Cabrera

Abstract read
In one paragraph

Article in Drug discovery today. Disease models, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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 3 institutions in 2 countries.

Nicola LaiCenter for Modeling Integrated Metabolic Systems, Case Western Reserve University, Cleveland, Ohio. U.S.A.
L Bruce GladdenDepartment of Kinesiology, Auburn University, Auburn, Alabama. U.S.A.
Pierre G CarlierInstitute of Myology, NMR Laboratory, F-75651 Paris, France ; CEA, I BM, MIRCen, IdM NMR Laboratory, F-75651 Paris, France ; UPMC Univ Paris 06, F-75005 Paris, France.
Marco E CabreraCenter for Modeling Integrated Metabolic Systems, Case Western Reserve University, Cleveland, Ohio. U.S.A.
Case Western Reserve University · USAuburn University · USInstitut de Myologie · FR

Funding

CORE--SYSTEM MODELING INTEGRATIONP50GM066309 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI SAIDEL, GERALD M · 2002 to 2006
$11.4M
NIGMS NIH HHS P50 GM066309
6 · The paper itself

Abstract

How does skeletal muscle manage to regulate the pathways of ATP synthesis during large-scale changes in work rate while maintaining metabolic homeostasis remains unknown. The classic model of metabolic regulation during muscle contraction states that accelerating ATP utilization leads to increasing concentrations of ADP and Pi, which serve as substrates for oxidative phosphorylation and thus accelerate ATP synthesis. An alternative model states that both the ATP demand and ATP supply pathways are simultaneously activated. Here, we review experimental and computational models of muscle contraction and energetics at various organizational levels and compare them with respect to their pros and cons in facilitating understanding of the regulation of energy metabolism during exercise in the intact organism.

Indexed as

computer modelsenergy metabolismexercisein vivo modelsregulationsingle fiber

Identifiers

PMID24421861
PMCPMC3888514
OpenAlexW2001585357

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.