Evidence map›Paper›PMID 31947691›Full record

ArticleInternational journal of molecular sciences2020

Suppression of β1-Adrenoceptor Autoantibodies is Involved in the Antiarrhythmic Effects of Omega-3 Fatty Acids in Male and Female Hypertensive Rats.

Barbara Szeiffova Bacova, Jana Radosinska, Gerd Wallukat, Miroslav Barancik, Anne Wallukat, Vladimir Knezl, Matus Sykora, Ludovit Paulis, Narcis Tribulova

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 5 institutions in 2 countries.

Barbara Szeiffova BacovaCentre of Experimental Medicine, Institute for Heart Research, SAS, 841 04 Bratislava, Slovakia.
Jana RadosinskaDepartment of Physiology, Faculty of Medicine, Comenius University, 81108 Bratislava, Slovakia.
Gerd WallukatMax-Delbruck Centrum für Molekulare Medizine, 13125 Berlin, Germany.
Miroslav BarancikCentre of Experimental Medicine, Institute for Heart Research, SAS, 841 04 Bratislava, Slovakia.
Anne WallukatBerlin Cures GmbH, 10719 Berlin, Germany.
Vladimir KnezlCenter of Experimental Medicine SAS, Institute of Experimental Pharmacology and Toxicology, 841 04 Bratislava, Slovakia.
Matus SykoraCentre of Experimental Medicine, Institute for Heart Research, SAS, 841 04 Bratislava, Slovakia.
Ludovit PaulisInstitute of Pathophysiology, Faculty of Medicine, Comenius University, 81108 Bratislava, Slovakia.
Narcis TribulovaCentre of Experimental Medicine, Institute for Heart Research, SAS, 841 04 Bratislava, Slovakia.
Centre of Experimental Medicine of the Slovak Academy of Sciences · SKComenius University Bratislava · SKBerlin Heart (Germany) · DEInstitute of Experimental Pharmacology and Toxicology of the Slovak Academy of Sciences · SKMax Delbrück Center · DE

Funding

Agentúra na Podporu Výskumu a Vývoja 18-0548, 15-0376EU ITMS 26230120009Vedecká Grantová Agentúra MŠVVaŠ SR a SAV 2/0002/20, 2/0158/19
6 · The paper itself

Abstract

The arrhythmogenic potential of β1-adrenoceptor autoantibodies (β1-AA), as well as antiarrhythmic properties of omega-3 in heart diseases, have been reported while underlying mechanisms are poorly understood. We aimed to test our hypothesis that omega-3 (eicosapentaenoic acid-EPA, docosahexaenoic acid-DHA) may inhibit matrix metalloproteinase (MMP-2) activity to prevent cleavage of β1-AR and formation of β1-AA resulting in attenuation of pro-arrhythmic connexin-43 (Cx43) and protein kinase C (PKC) signaling in the diseased heart. We have demonstrated that the appearance and increase of β1-AA in blood serum of male and female 12-month-old spontaneously hypertensive rats (SHR) was associated with an increase of inducible ventricular fibrillation (VF) comparing to normotensive controls. In contrast, supplementation of hypertensive rats with omega-3 for two months suppressed β1-AA levels and reduced incidence of VF. Suppression of β1-AA was accompanied by a decrease of elevated myocardial MMP-2 activity, preservation of cardiac cell membrane integrity and Cx43 topology. Moreover, omega-3 abrogated decline in expression of total Cx43 as well as its phosphorylated forms at serine 368 along with PKC-ε, while decreased pro-fibrotic PKC-δ levels in hypertensive rat heart regardless the sex. The implication of MMP-2 in the action of omega-3 was also demonstrated in cultured cardiomyocytes in which desensitization of β1-AR due to permanent activation of β1-AR with isoproterenol was prevented by MMP-2 inhibitor or EPA. Collectively, these data support the notion that omega-3 via suppression of β1-AA mechanistically controlled by MMP-2 may attenuate abnormal of Cx43 and PKC

Indexed as

AnimalsAnti-Arrhythmia AgentsArrhythmias, CardiacAutoantibodiesAutoantigensBiomarkersCell MembraneConnexin 43Disease Models, AnimalDisease SusceptibilityFatty Acids, Omega-3FemaleHypertensionMaleMatrix Metalloproteinase 2Myocytes, CardiacAnti-Arrhythmia AgentsAutoantibodiesAutoantigensBiomarkersConnexin 43Fatty Acids, Omega-3Gja1 protein, ratMatrix Metalloproteinase 2Protein Kinase C-epsilonReceptors, Adrenergic, beta-1autoantibodyconnexin-43essential hypertensionlethal arrhythmiasomega-3rats

Identifiers

PMID31947691
PMCPMC7013542
OpenAlexW2998911611

What OpenQuestion holds

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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.