Evidence map›Paper›PMID 26729111›Full record

ReviewInternational journal of molecular sciences2016

Cardiovascular Dysfunction Following Burn Injury: What We Have Learned from Rat and Mouse Models.

Ashley N Guillory, Robert P Clayton, David N Herndon, Celeste C Finnerty

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03085420 (Cardiac Arrhythmias and Dysfunction in the Pediatric Burn Patient), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.5field-weighted citation impact, top 4% 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.

NCT03085420 naterminatednot on this mapstarted 2017, after this paper: background citation

Cardiac Arrhythmias and Dysfunction in the Pediatric Burn Patient

TypeinterventionalSponsorShriners Hospitals for ChildrenRan2017 to 2018Enrolled10ConditionsCardiac DysfunctionArmsEchocardiogram
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Post-burn Lung Inflammation Is Associated With Induction of Pulmonary Cathelicidin-related Antimicrobial Peptide and S100a8 in Mice.Journal of burn care & research : official publication of the American Burn Association · 2025
    Article
  5. Article
  6. Epigenetic orchestration of RNA mInternational journal of biological sciences · 2025
    Review
  7. Review
  8. Pathophysiology of Severe Burn Injuries: New Therapeutic Opportunities From a Systems Perspective.Journal of burn care & research : official publication of the American Burn Association · 2024
    Review
  9. Review
  10. Article
  11. [Research advances on post-burn cognitive disorders and its mechanism].Zhonghua shao shang yu chuang mian xiu fu za zhi · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Small animal models of thermal injury.Methods in cell biology · 2022
    Review
  19. Review
  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 1 institution in 1 country.

Ashley N GuilloryDepartment of Surgery, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, USA. asguillo@utmb.edu.
Robert P ClaytonInstitute for Translational Sciences, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, USA. rpclayto@utmb.edu.
David N HerndonDepartment of Surgery, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, USA. dherndon@utmb.edu.
Celeste C FinnertyDepartment of Surgery, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, USA. ccfinner@utmb.edu.
The University of Texas Medical Branch at Galveston · US

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
Project 9: The role of androgen/corticosteroid in fat, muscle and glucose metabolism of burn victimsP50GM060338 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI FINNERTY, CELESTE CAMPBELL · 2000 to 2017
$24.2M
UTMB CLINICAL AND TRANSLATIONAL SCIENCE AWARD: NASA BED REST STUDIESUL1RR029876 · NCRR · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2009 to 2011
$17.7M
MODULATION OF THE POSTBURN HYPERMETABOLIC RESPONSER01GM056687 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 1998 to 2017
$9.0M
UTMB Clinical and Translational Science AwardKL2TR001441 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI AMEREDES, BILL T · 2015 to 2024
$4.0M
POSTDOCTORAL TRAINING IN TRAUMA &BURNST32GM008256 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI Celeste Campbell Finnerty, Oscar E. Suman-Vejas · 1990 to 2026
$4.0M
UTMB Clinical and Translational Science AwardTL1TR001440 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HOMMEL, JONATHAN DEAN · 2015 to 2024
$3.4M
Effects of Chronic Catecholamine Exposure on Post-burn ScarringR01GM112936 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI FINNERTY, CELESTE CAMPBELL · 2015 to 2019
$1.8M
UTMB Clinical and Translational Science AwardKL2RR029875 · NCRR · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2009 to 2011
$609k
NCATS NIH HHS KL2 TR001441NCATS NIH HHS TL1 TR001440NCATS NIH HHS UL1 TR001439NCATS NIH HHS UL1TR001439NCRR NIH HHS KL2 RR029875NCRR NIH HHS KL2RR029875NCRR NIH HHS UL1 RR029876NCRR NIH HHS UL1RR029876NIGMS NIH HHS P50 GM060338NIGMS NIH HHS P50-GM060338NIGMS NIH HHS R01 GM056687NIGMS NIH HHS R01-GM056687-11NIGMS NIH HHS R01 GM112936NIGMS NIH HHS R01-GM112936NIGMS NIH HHS T32 GM008256NIGMS NIH HHS T32-GM008256
6 · The paper itself

Abstract

Severe burn profoundly affects organs both proximal and distal to the actual burn site. Cardiovascular dysfunction is a well-documented phenomenon that increases morbidity and mortality following a massive thermal trauma. Beginning immediately post-burn, during the ebb phase, cardiac function is severely depressed. By 48 h post-injury, cardiac function rebounds and the post-burn myocardium becomes tachycardic and hyperinflammatory. While current clinical trials are investigating a variety of drugs targeted at reducing aspects of the post-burn hypermetabolic response such as heart rate and cardiac work, there is still a paucity of knowledge regarding the underlying mechanisms that induce cardiac dysfunction in the severely burned. There are many animal models of burn injury, from rodents, to sheep or swine, but the majority of burn related cardiovascular investigations have occurred in rat and mouse models. This literature review consolidates the data supporting the prevalent role that β-adrenergic receptors play in mediating post-burn cardiac dysfunction and the idea that pharmacological modulation of this receptor family is a viable therapeutic target for resolving burn-induced cardiac deficits.

Indexed as

AnimalsBurnsCardiovascular DiseasesCardiovascular SystemDisease Models, AnimalHumansMiceMolecular Targeted TherapyRatsReceptors, Adrenergic, betaReceptors, Adrenergic, betaanimal modelsburnscardiac dysfunctionthermal injury

Identifiers

PMID26729111
PMCPMC4730298
OpenAlexW2220333480

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.