Evidence map›Paper›PMID 25263208›Full record

ArticlePhysiological reports2014

Relating tissue/organ energy expenditure to metabolic fluxes in mouse and human: experimental data integrated with mathematical modeling.

China M Kummitha, Satish C Kalhan, Gerald M Saidel, Nicola Lai

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Aberrant Energy Metabolism in Alzheimer's Disease.Journal of translational internal medicine · 2022
    Article
  9. Circadian REV-ERBs repressNature cardiovascular research · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Metabolic responses to intermittent hypoxia are regulated by sex and estradiol in mice.American journal of physiology. Endocrinology and metabolism · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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.

China M KummithaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio, USA.
Satish C KalhanDepartment of Pathobiology, Cleveland Clinic, Lerner Research Institute, Cleveland, Ohio, USA.
Gerald M SaidelDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio, USA.
Nicola LaiDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio, USA Department of Pediatrics, Case Western Reserve University, Cleveland, Ohio, USA.
Case Western Reserve University · USCleveland Clinic Lerner College of Medicine · US

Funding

Translational Research in Cystic FibrosisP30DK027651 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI DRUMM, MITCHELL L · 1986 to 2014
$15.6M
Systems Biology Approach to Growth Regulation in Cystic FibrosisR01GM088823 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI DRUMM, MITCHELL L · 2009 to 2012
$1.6M
Systems Biology Investigation of Muscle Exercise Metabolism in DiabetesK25AR057206 · NIAMS · OLD DOMINION UNIVERSITY · PI LAI, NICOLA · 2011 to 2015
$593k
NIAMS NIH HHS K25 AR057206NIDDK NIH HHS P30 DK027651NIGMS NIH HHS R01 GM088823
6 · The paper itself

Abstract

Mouse models of human diseases are used to study the metabolic and physiological processes leading to altered whole-body energy expenditure (EE), which is the sum of EE of all body organs and tissues. Isotopic techniques, arterio-venous difference of substrates, oxygen, and blood flow measurements can provide essential information to quantify tissue/organ EE and substrate oxidation. To complement and integrate experimental data, quantitative mathematical model analyses have been applied in the design of experiments and evaluation of metabolic fluxes. In this study, a method is presented to quantify the energy expenditure of the main mouse organs using metabolic flux measurements. The metabolic fluxes and substrate utilization of the main metabolic pathways of energy metabolism in the mouse tissue/organ systems and the whole body are quantified using a mathematical model based on mass and energy balances. The model is composed of six organ/tissue compartments: brain, heart, liver, gastrointestinal tract, muscle, and adipose tissue. Each tissue/organ is described with a distinct system of metabolic reactions. This model quantifies metabolic and energetic characteristics of mice under overnight fasting conditions. The steady-state mass balances of metabolites and energy balances of carbohydrate and fat are integrated with available experimental data to calculate metabolic fluxes, substrate utilization, and oxygen consumption in each tissue/organ. The model serves as a paradigm for designing experiments with the minimal reliable measurements necessary to quantify tissue/organs fluxes and to quantify the contributions of tissue/organ EE to whole-body EE that cannot be easily determined currently.

Indexed as

Energy metabolismflux balance analysismetabolic pathway fluxesoxygen consumptionsubstrate utilization

Identifiers

PMID25263208
PMCPMC4270223
OpenAlexW2096430209

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.