Evidence map›Paper›PMID 25485899›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2015

Obesity superimposed on aging magnifies inflammation and delays the resolving response after myocardial infarction.

Elizabeth F Lopez, Janusz H Kabarowski, Kevin A Ingle, Vasundhara Kain, Stephen Barnes, David K Crossman, Merry L Lindsey, Ganesh V Halade

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 4 pooled it
5.8field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 4 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Guidelines for in vivo mouse models of myocardial infarction.American journal of physiology. Heart and circulatory physiology · 2021
    Guideline
  3. Guidelines for experimental models of myocardial ischemia and infarction.American journal of physiology. Heart and circulatory physiology · 2018
    Guideline
  4. Guidelines for authors and reviewers on antibody use in physiology studies.American journal of physiology. Heart and circulatory physiology · 2018
    Guideline
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Guidelines on antibody use in physiology research.American journal of physiology. Renal physiology · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
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  18. Article
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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

8 authors at 3 institutions in 1 country.

Elizabeth F LopezThe University of Texas Medical Branch, Galveston, Texas;
Janusz H KabarowskiDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama;
Kevin A IngleDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama;
Vasundhara KainDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama;
Stephen BarnesTargeted Metabolomics and Proteomics Laboratory, The University of Alabama at Birmingham, Birmingham, Alabama; Department of Pharmacology and Toxicology, The University of Alabama at Birmingham, Birmingham, Alabama;
David K CrossmanDepartment of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama; and.
Merry L LindseyMississippi Center for Heart Research, Department of Physiology and Biophysics, University of Mississippi Medical Center, and Research Service, G.V. (Sonny) Montgomery Veterans Affairs Medical Center, Jackson, Mississippi.
Ganesh V HaladeDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama; halade@uab.edu.
University of Alabama at Birmingham · USThe University of Texas Medical Branch at Galveston · USUniversity of Mississippi Medical Center · US

Funding

STRUCTURAL VASCULAR ADAPTATION OF THE MICROCIRCULATIONP01HL051971 · NHLBI · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI HALL, JOHN E · 1993 to 2018
$39.4M
UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
The Role of Macrophage-derived MMPs in LV RemodelingR01HL075360 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LINDSEY, MERRY L. · 2004 to 2018
$5.4M
DHA Mechanisms in Obesity-mediated Cardiac Remodeling Post-Myocardial InfarctionR00AT006704 · NCCIH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HALADE, GANESH V · 2013 to 2015
$717k
Neutrophil Polarization Following Myocardial InfarctionI01BX000505 · VA · VETERANS HEALTH ADMINISTRATION · PI LINDSEY, MERRY L. · 2009 to 2024
–
BLRD VA 5I01BX000505BLRD VA I01 BX000505NCCIH NIH HHS R00 AT006704NCCIH NIH HHS R00-AT-006704NHLBI NIH HHS HL051971NHLBI NIH HHS N01-HV-00244NHLBI NIH HHS P01 HL051971NHLBI NIH HHS R01 HL075360NHLBI NIH HHS R01-HL-075360NIDDK NIH HHS P30 DK079337NIDDK NIH HHS P30-DK-079337PHS HHS HHSN 268201000036C
6 · The paper itself

Abstract

Polyunsaturated fatty acid (PUFA) intake has increased over the last 100 yr, contributing to the current obesogenic environment. Obesity and aging are prominent risk factors for myocardial infarction (MI). How obesity interacts with aging to alter the post-MI response, however, is unclear. We tested the hypothesis that obesity in aging mice would impair the resolution of post-MI inflammation. PUFA diet (PUFA aging group) feeding to 12-mo-old C57BL/6J mice for 5 mo showed higher fat mass compared with standard lab chow (LC)-fed young (LC young group; 3-5 mo old) or aging alone control mice (LC aging group). LC young, LC aging, and PUFA aging mice were subjected to coronary artery ligation to induce MI. Despite similar infarct areas post-MI, plasma proteomic profiling revealed higher VCAM-1 in the PUFA aging group compared with LC young and LC aging groups, leading to increased neutrophil infiltration in the PUFA aging group (P<0.05). Macrophage inflammatory protein-1γ and CD40 were also increased at day 1, and myeloperoxidase remained elevated at day 5, an observation consistent with delayed wound healing in the PUFA aging group. Lipidomic analysis showed higher levels of arachidonic acid and 12(S)-hydroxyeicosatetraenoic acid at day 1 post-MI in the PUFA aging group compared with the LC aging group (all P<0.05), thereby mediating neutrophil extravasation in the PUFA aging group. The inflammation-resolving enzymes 5-lipoxygenase, cyclooxygenase-2, and heme oxyegnase-1 were altered to delay wound healing post-MI in the PUFA aging group compared with LC young and LC aging groups. PUFA aging magnifies the post-MI inflammatory response and impairs the healing response by stimulating prolonged neutrophil trafficking and proinflammatory lipid mediators.

Indexed as

12-Hydroxy-5,8,10,14-eicosatetraenoic AcidAgingAnimalsArachidonic AcidCD40 AntigensCyclooxygenase 2Diet, High-FatFatty Acids, Omega-3Heme Oxygenase-1InflammationLipoxygenaseMacrophage Inflammatory ProteinsMiceMice, Inbred C57BLMyocardial InfarctionNeutrophil Infiltration12-Hydroxy-5,8,10,14-eicosatetraenoic AcidArachidonic AcidCD40 AntigensCyclooxygenase 2Fatty Acids, Omega-3Heme Oxygenase-1LipoxygenaseMacrophage Inflammatory Proteinsinflammationlipid mediatorslipidomicsneutrophilspolyunsaturated fatty acidsproteomics

Identifiers

PMID25485899
PMCPMC4329482
OpenAlexW2106109608

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.