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Endothelin type A receptor blockade increases renoprotection in congestive heart failure combined with chronic kidney disease: Studies in 5/6 nephrectomized rats with aorto-caval fistula

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    SYSNO ASEP0568956
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEndothelin type A receptor blockade increases renoprotection in congestive heart failure combined with chronic kidney disease: Studies in 5/6 nephrectomized rats with aorto-caval fistula
    Author(s) Kala, P. (CZ)
    Vaňourková, Z. (CZ)
    Škaroupková, P. (CZ)
    Kompanowska - Jezierska, E. (PL)
    Sadowski, J. (PL)
    Walkowska, A. (PL)
    Veselka, J. (CZ)
    Táborský, M. (CZ)
    Maxová, H. (CZ)
    Vaněčková, Ivana (FGU-C) RID, ORCID
    Červenka, L. (CZ)
    Number of authors11
    Article number114157
    Source TitleBiomedicine & Pharmacotherapy. - : Elsevier - ISSN 0753-3322
    Roč. 158, February (2023)
    Number of pages11 s.
    Languageeng - English
    CountryFR - France
    Keywordscongestive heart failure ; chronic kidney disease ; endothelin system ; endothelin receptor type A ; aorto-caval fistula ; 5/6 nephrectomy
    OECD categoryCardiac and Cardiovascular systems
    R&D ProjectsLX22NPO5104 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportFGU-C - RVO:67985823
    UT WOS000916209900001
    EID SCOPUS85145296028
    DOI10.1016/j.biopha.2022.114157
    AnnotationBackground: Association of congestive heart failure (CHF) and chronic kidney disease (CKD) worsens the patient's prognosis and results in poor survival rate. The aim of this study was to examine if addition of endothelin type A (ETA) receptor antagonist to the angiotensin-converting enzyme inhibitor (ACEi) will bring additional beneficial effects in experimental rats.Methods: CKD was induced by 5/6 renal mass reduction (5/6 NX) and CHF was elicited by volume overload achieved by creation of aorto-caval fistula (ACF). The follow-up was 24 weeks after the first intervention (5/6 NX). The treatment regimens were initiated 6 weeks after 5/6 NX and 2 weeks after ACF creation.Results: The final survival in untreated group was 15%. The treatment with ETA receptor antagonist alone or ACEi alone and the combined treatment improved the survival rate to 64%, 71% and 75%, respectively, however, the difference between the combination and either single treatment regimen was not significant. The combined treatment exerted best renoprotection, causing additional reduction in albuminuria and reducing renal glomerular and tubulointerstitial injury as compared with ACE inhibition alone.Conclusions: Our results show that treatment with ETA receptor antagonist attenuates the CKD-and CHF-related mortality, and addition of ETA receptor antagonist to the standard blockade of RAS by ACEi exhibits additional renoprotective actions.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2024
    Electronic addresshttps://doi.org/10.1016/j.biopha.2022.114157
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