Evidence map›Paper›PMID 30979784›Full record

ArticleClinical science (London, England : 1979)2019

Epoxyeicosatrienoic acid analog EET-B attenuates post-myocardial infarction remodeling in spontaneously hypertensive rats.

Jan Neckář, Md Abdul Hye Khan, Garrett J Gross, Michaela Cyprová, Jaroslav Hrdlička, Alena Kvasilová, John R Falck, William B Campbell, Lenka Sedláková, Šárka Škutová and 5 more

Open access · greenAbstract read
In one paragraph

Article in Clinical science (London, England : 1979), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  14. Eicosanoids: Atherosclerosis and cardiometabolic health.Journal of clinical & translational endocrinology · 2020
    Review
  15. Review
  16. Orally Active Epoxyeicosatrienoic Acid Analogs.Journal of cardiovascular pharmacology · 2017
    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

15 authors at 4 institutions in 2 countries.

Jan NeckářDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, U.S.A. jan.neckar@fgu.cas.cz.ORCID 0000-0002-1187-9992
Md Abdul Hye KhanDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, U.S.A.
Garrett J GrossDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, U.S.A.
Michaela CyprováDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Jaroslav HrdličkaDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Alena KvasilováInstitute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czech Republic.
John R FalckDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, U.S.A.
William B CampbellDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, U.S.A.
Lenka SedlákováDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Šárka ŠkutováDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Veronika OlejníčkováDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
Martina GregorovičováDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
David SedmeraDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
František KolářDepartment of Developmental Cardiology, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.
John D ImigDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI, U.S.A.
Czech Academy of Sciences · CZMedical College of Wisconsin · USCharles University · CZThe University of Texas Southwestern Medical Center · US

Funding

Eicosanoid-based Therapy for DiabetesR01DK103616 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI IMIG, JOHN D · 2015 to 2019
$2.4M
EET-Induced Cardioprotection: Role of Opioids and Nitric Oxide (NO)R01HL111392 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI AUCHAMPACH, JOHN A · 2012 to 2016
$2.2M
Substance P: A central mediator of cardiac fibrosis and diastolic dysfunctionR01HL132908 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI CAMPBELL, WILLIAM BRYSON · 2017 to 2020
$1.4M
NHLBI NIH HHS R01 HL111392NHLBI NIH HHS R01 HL132908NIDDK NIH HHS R01 DK103616
6 · The paper itself

Abstract

Epoxyeicosatrienoic acids (EETs) and their synthetic analogs have cardiovascular protective effects. Here, we investigated the action of a novel EET analog EET-B on the progression of post-myocardial infarction (MI) heart failure in spontaneously hypertensive rats (SHR). Adult male SHR were divided into vehicle- and EET-B (10 mg/kg/day; p.o., 9 weeks)-treated groups. After 2 weeks of treatment, rats were subjected to 30-min left coronary artery occlusion or sham operation. Systolic blood pressure (SBP) and echocardiography (ECHO) measurements were performed at the beginning of study, 4 days before, and 7 weeks after MI. At the end of the study, tissue samples were collected for histological and biochemical analyses. We demonstrated that EET-B treatment did not affect blood pressure and cardiac parameters in SHR prior to MI. Fractional shortening (FS) was decreased to 18.4 ± 1.0% in vehicle-treated MI rats compared with corresponding sham (30.6 ± 1.0%) 7 weeks following MI induction. In infarcted SHR hearts, EET-B treatment improved FS (23.7 ± 0.7%), markedly increased heme oxygenase-1 (HO-1) immunopositivity in cardiomyocytes and reduced cardiac inflammation and fibrosis (by 13 and 19%, respectively). In conclusion, these findings suggest that EET analog EET-B has beneficial therapeutic actions to reduce cardiac remodeling in SHR subjected to MI.

Indexed as

AnimalsArachidonic AcidsBlood PressureDisease Models, AnimalHeartHeme Oxygenase-1HumansMaleMyocardial InfarctionRatsRats, Inbred SHRArachidonic AcidsHeme Oxygenase-1blood pressureepoxyeicosatrienoic acidheart failuremyocardial infarctionspontaneously hypertensive rat

Identifiers

PMID30979784
PMCPMC6492034
OpenAlexW2936175424

What Socratic 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 Socratic graph.