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Effects of Combined Endothelin A Receptor and Renin-Angiotensin System Blockade on the Course of End-Organ Damage in 5/6 Nephrectomized Ren-2 Hypertensive Rats

  1. 1.
    SYSNO ASEP0390670
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEffects of Combined Endothelin A Receptor and Renin-Angiotensin System Blockade on the Course of End-Organ Damage in 5/6 Nephrectomized Ren-2 Hypertensive Rats
    Author(s) Vaněčková, Ivana (FGU-C) RID, ORCID
    Kujal, P. (CZ)
    Husková, Z. (CZ)
    Vaňourková, Z. (CZ)
    Vernerová, Z. (CZ)
    Čertíková - Chábová, V. (CZ)
    Škaroupková, P. (CZ)
    Kramer, H. J. (DE)
    Tesař, V. (CZ)
    Červenka, L. (CZ)
    Source TitleKidney & Blood Pressure Research. - : Karger - ISSN 1420-4096
    Roč. 35, č. 5 (2012), s. 382-392
    Number of pages11 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywords5/6 nephrectomy ; Endothelin receptor type A ; AT1 receptor blocker ; end-organ damage ; hypertension
    Subject RIVFA - Cardiovascular Diseases incl. Cardiotharic Surgery
    CEZAV0Z50110509 - FGU-C (2005-2011)
    UT WOS000305594600011
    DOI10.1159/000336823
    AnnotationThe additive effect of endothelin-1 blockade to renin-angiotensin blockade was evaluated in rats with ablation nephrectomy. While RAS blockade normalized blood pressure (BP), improved survival, decreased cardiac hypertrophy and proteinuria as well as tissue angiotensin II and ET-1 levels, ETA receptor blockade only partially improved survival rate, reduced BP, attenuated the development of cardiac hypertrophy and transiently reduced proteinuria. No additive cardio- and renoprotective effects of ETA and RAS blockade were noted at the end of the study suggesting that the RAS system is the main target for antihypertensive treatment in models with inappropriately activated RAS
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2013
Number of the records: 1  

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