Evidence map›Paper›PMID 34440257›Full record

ArticleBiomedicines2021

Effects of Epoxyeicosatrienoic Acid-Enhancing Therapy on the Course of Congestive Heart Failure in Angiotensin II-Dependent Rat Hypertension: From mRNA Analysis towards Functional In Vivo Evaluation.

Petr Kala, Matúš Miklovič, Šárka Jíchová, Petra Škaroupková, Zdeňka Vaňourková, Hana Maxová, Olga Gawrys, Elzbieta Kompanowska-Jezierska, Janusz Sadowski, John D Imig and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05305170 (Plasmatic Levels of Epoxyeicosatrienoic and Dihydroxyeicosatrienoic Acids in Heart Failure), which is not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT05305170 unknown statusnot on this map

Plasmatic Levels of Epoxyeicosatrienoic and Dihydroxyeicosatrienoic Acids in Heart Failure

Typeobservational_patient_registrySponsorUniversity Hospital, MotolRan2021 to 2024Enrolled100ConditionsHeart FailureArmsLevels of EETs, DHETs and HETEs
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

17 authors.

Petr KalaDepartment of Cardiology, University Hospital Motol and 2nd Faculty of Medicine, Charles University, 150 06 Prague, Czech Republic.ORCID 0000-0001-5626-7706
Matúš MiklovičCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0003-0427-2583
Šárka JíchováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0002-3506-1116
Petra ŠkaroupkováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Zdeňka VaňourkováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Hana MaxováDepartment of Pathophysiology, 2nd Faculty of Medicine, Charles University, 150 06 Prague, Czech Republic.
Olga GawrysCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0002-4397-3991
Elzbieta Kompanowska-JezierskaDepartment of Renal and Body Fluid Physiology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106 Warsaw, Poland.
Janusz SadowskiDepartment of Renal and Body Fluid Physiology, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106 Warsaw, Poland.ORCID 0000-0002-9701-5334
John D ImigDrug Discovery Center, Medical College of Wisconsin, Wauwatosa, WI 53226, USA.
John R FalckDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-9219-7845
Josef VeselkaDepartment of Cardiology, University Hospital Motol and 2nd Faculty of Medicine, Charles University, 150 06 Prague, Czech Republic.
Luděk ČervenkaCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Renáta AiglováDepartment of Internal Medicine I, Cardiology, University Hospital Olomouc and Palacký University, I.P. Pavlova 185/6, Nová Ulice, 779 00 Olomouc, Czech Republic.
Marek VíchaDepartment of Internal Medicine I, Cardiology, University Hospital Olomouc and Palacký University, I.P. Pavlova 185/6, Nová Ulice, 779 00 Olomouc, Czech Republic.
Vít GlogerDepartment of Internal Medicine I, Cardiology, University Hospital Olomouc and Palacký University, I.P. Pavlova 185/6, Nová Ulice, 779 00 Olomouc, Czech Republic.
Miloš TáborskýDepartment of Internal Medicine I, Cardiology, University Hospital Olomouc and Palacký University, I.P. Pavlova 185/6, Nová Ulice, 779 00 Olomouc, Czech Republic.

Funding

Ministerstvo Zdravotnictví Ceské Republiky 17-28220AUniverzita Karlova v Praze 68121Welch Foundation I-0011
6 · The paper itself

Abstract

This study evaluates the effects of chronic treatment with EET-A, an orally active epoxyeicosatrienoic acid (EETs) analog, on the course of aorto-caval fistula (ACF)-induced heart failure (HF) in Ren-2 transgenic rats (TGR), a model characterized by hypertension and augmented activity of the renin-angiotensin system (RAS). The results were compared with standard pharmacological blockade of the RAS using angiotensin-converting enzyme inhibitor (ACEi). The rationale for employing EET-A as a new treatment approach is based on our findings that apart from increased RAS activity, untreated ACF TGR also shows kidney and left ventricle (LV) tissue deficiency of EETs. Untreated ACF TGR began to die 17 days after creating ACF and were all dead by day 84. The treatment with EET-A alone or ACEi alone improved the survival rate: in 156 days after ACF creation, it was 45.5% and 59.4%, respectively. The combined treatment with EET-A and ACEi appeared to improve the final survival to 71%; however, the difference from either single treatment regimen did not reach significance. Nevertheless, our findings support the notion that targeting the cytochrome P-450-dependent epoxygenase pathway of arachidonic acid metabolism should be considered for the treatment of HF.

Indexed as

angiotensin-converting enzyme inhibitoraorto-caval fistulacongestive heart failurecytochrome P-450epoxyeicosatrienoic acidshypertensionRen-2 transgenic ratsrenin-angiotensin systemvolume-overload heart failure

Identifiers

PMID34440257
PMCPMC8393645

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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.