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IL-1 receptor blockade alleviates endotoxin-mediated impairment of renal drug excretory functions in rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F15%3A10296775" target="_blank" >RIV/00216208:11110/15:10296775 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/15:10296775 RIV/00216208:11160/15:10296775

  • Result on the web

    <a href="http://ajprenal.physiology.org/content/308/5/F388.full" target="_blank" >http://ajprenal.physiology.org/content/308/5/F388.full</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1152/ajprenal.00266.2014" target="_blank" >10.1152/ajprenal.00266.2014</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    IL-1 receptor blockade alleviates endotoxin-mediated impairment of renal drug excretory functions in rats

  • Original language description

    The aim of our study was to investigate whether two potent anti-inflammatory agents, dexamethasone and anakinra, an IL-1 receptor antagonist, may influence acute kidney injury (AKI) and associated drug excretory functions during endotoxemia (LPS) in rats. Ten hours after LPS administration, untreated endotoxemic rats developed typical symptoms of AKI, with reduced GFR, impaired tubular excretion of urea and sodium, and decreased urinary excretion of azithromycin, an anionic substrate for multidrug resistance-transporting proteins. Administration of both immunosuppressants attenuated the inflammatory response, liver damage, AKI, and increased renal clearance of azithromycin mainly by restoration of GFR, without significant influence on its tubular secretion. The lack of such an effect was related to the differential effect of both agents on the renal expression of individual drug transporters. Only dexamethasone increased the urinary clearance of bile acids, in accordance with the reduc

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/EE2.3.30.0061" target="_blank" >EE2.3.30.0061: Increasing of the R&D capacity at Charles University through new positions for graduates of doctoral studies</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    American Journal of Physiology - Renal Physiology

  • ISSN

    1931-857X

  • e-ISSN

  • Volume of the periodical

    308

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    "F388"-"F399"

  • UT code for WoS article

    000350811800002

  • EID of the result in the Scopus database

    2-s2.0-84924075862