Evidence map›Paper›PMID 30054426›Full record

ArticleBioscience reports2018

20-Hydroxyeicosatetraenoic acid antagonist attenuates the development of malignant hypertension and reverses it once established: a study in Cyp1a1-Ren-2 transgenic rats.

Lenka Sedláková, Soňa Kikerlová, Zuzana Husková, Lenka Červenková, Věra Čertíková Chábová, Josef Zicha, John R Falck, John D Imig, Elzbieta Kompanowska-Jezierska, Janusz Sadowski and 3 more

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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  7. The role of Elabela in kidney disease.International urology and nephrology · 2021
    Review
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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

13 authors at 5 institutions in 3 countries.

Lenka SedlákováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Soňa KikerlováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Zuzana HuskováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Lenka ČervenkováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Věra Čertíková ChábováCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Josef ZichaInstitute of of Physiology, Czech Academy of Sciences, Prague, Czech Republic.
John R FalckDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, U.S.A.
John D ImigDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, WI, U.S.A.
Elzbieta Kompanowska-JezierskaDepartment of Renal and Body Fluid Physiology, M. Mossakowski Medical Research Centre, Polish Academy of Science, Warsaw, Poland.
Janusz SadowskiDepartment of Renal and Body Fluid Physiology, M. Mossakowski Medical Research Centre, Polish Academy of Science, Warsaw, Poland.
Vojtěch KrátkýCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Luděk ČervenkaCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Libor KopkanCenter for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic libor.kopkan@ikem.cz.
Institute of Clinical and Experimental Medicine · CZMossakowski Medical Research Institute, Polish Academy of Sciences · PLCharles University · CZCzech Academy of Sciences · CZThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We hypothesized that vascular actions of 20-hydroxyeicosatetraenoic acid (20-HETE), the product of cytochrome P450 (CYP450)-dependent ω-hydroxylase, potentiate prohypertensive actions of angiotensin II (ANG II) in Cyp1a1-Ren-2 transgenic rats, a model of ANG II-dependent malignant hypertension. Therefore, we evaluated the antihypertensive effectiveness of 20-HETE receptor antagonist (AAA) in this model. Malignant hypertension was induced in Cyp1a1-Ren-2 transgenic rats by activation of the

Indexed as

AmidesAngiotensin IIAngiotensin II Type 1 Receptor BlockersAnimalsAntihypertensive AgentsCytochrome P-450 CYP1A1Hydroxyeicosatetraenoic AcidsHypertension, MalignantIndolesKidneyMaleRats, Transgenic20-hydroxy-5,8,11,14-eicosatetraenoic acidAmidesAngiotensin IIAngiotensin II Type 1 Receptor BlockersAntihypertensive AgentsCytochrome P-450 CYP1A1Hydroxyeicosatetraenoic Acidsindole-3-carbinolIndoles20-hydroxyeicosatetraenoic acidcytochrome p450 metabolitesmalignant hypertensionrenin-angiotensin system

Identifiers

PMID30054426
PMCPMC6131326
OpenAlexW2882997456

What OpenQuestion holds

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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.