Evidence map›Paper›PMID 25626875›Full record

ArticlePhysiological reports2015

Fibroblast growth factor 2 is an essential cardioprotective factor in a closed-chest model of cardiac ischemia-reperfusion injury.

Stacey L House, Joy Wang, Angela M Castro, Carla Weinheimer, Attila Kovacs, David M Ornitz

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. FGF family in health and disease.Molecular biomedicine · 2026
    Review
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  8. Characterization of a robust mouse model of heart failure with preserved ejection fraction.American journal of physiology. Heart and circulatory physiology · 2023
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
  16. Review
  17. Article
  18. Review
  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

6 authors at 1 institution in 1 country.

Stacey L HouseDivision of Emergency Medicine, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA Department of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Joy WangDivision of Emergency Medicine, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA Department of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Angela M CastroDepartment of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Carla WeinheimerCenter for Cardiovascular Research, Department of Medicine, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Attila KovacsCenter for Cardiovascular Research, Department of Medicine, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
David M OrnitzDepartment of Developmental Biology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Washington University in St. Louis · US

Funding

FIBROBLAST GROWTH FACTOR SIGNALING IN HEART INJURY AND REPAIRR01HL105732 · NHLBI · WASHINGTON UNIVERSITY · PI ORNITZ, DAVID M · 2011 to 2015
$1.9M
NHLBI NIH HHS R01 HL105732
6 · The paper itself

Abstract

Fibroblast growth factor 2 (FGF2) is cardioprotective in in vivo models of myocardial infarction; however, whether FGF2 has a protective role in in vivo ischemia-reperfusion (IR) injury, a model that more closely mimics acute myocardial infarction in humans, is not known. To assess the cardioprotective efficacy of endogenous FGF2, mice lacking a functional Fgf2 gene (Fgf2(-/-)) and wild-type controls were subjected to closed-chest regional cardiac IR injury (90 min ischemia, 7 days reperfusion). Fgf2(-/-) mice had significantly increased myocardial infarct size and significantly worsened cardiac function compared to wild-type controls at both 1 and 7 days post-IR injury. Pathophysiological analysis showed that at 1 day after IR injury Fgf2(-/-) mice have worsened cardiac strain patterns and increased myocardial cell death. Furthermore, at 7 days post-IR injury, Fgf2(-/-) mice showed a significantly reduced cardiac hypertrophic response, decreased cardiac vessel density, and increased vessel diameter in the peri-infarct area compared to wild-type controls. These data reveal both acute cardioprotective and a longer term proangiogenic potential of endogenous FGF2 in a clinically relevant, in vivo, closed-chest regional cardiac IR injury model that mimics acute myocardial infarction.

Indexed as

Cardiac repaircardioprotectionFGF2fibroblast growth factorischemia‐reperfusion injurymyocardial infarction

Identifiers

PMID25626875
PMCPMC4387743
OpenAlexW2157466039

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.