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Deferoxamine but not dexrazoxane alleviates liver injury induced by endotoxemia in rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F14%3A10272499" target="_blank" >RIV/00179906:_____/14:10272499 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/14:10272499 RIV/00216208:11160/14:10272499

  • Result on the web

    <a href="http://journals.lww.com/shockjournal/Fulltext/2014/10000/Deferoxamine_but_not_Dexrazoxane_Alleviates_Liver.13.aspx" target="_blank" >http://journals.lww.com/shockjournal/Fulltext/2014/10000/Deferoxamine_but_not_Dexrazoxane_Alleviates_Liver.13.aspx</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1097/SHK.0000000000000210" target="_blank" >10.1097/SHK.0000000000000210</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Deferoxamine but not dexrazoxane alleviates liver injury induced by endotoxemia in rats

  • Original language description

    The purpose of the present study was to compare the activity of two different clinically available iron chelators on the development of acute liver injury after administration of the bacterial endotoxin (lipopolysaccharide [LPS]) in rats. Lipopolysaccharide was administered either alone or after pretreatment with dexrazoxane (DEX) or deferoxamine (DFO). Control groups received only saline or its combination with either chelator. After 8 h, untreated LPS rats developed liver injury, with signs of inflammation and oxidative stress. Lipopolysaccharide reduced plasma iron concentrations in association with increased production of hepcidin and the reduced liver expression of ferroportin. Administration of chelating agents to LPS animals showed distinct effects. Although both drugs were able to reduce liver iron content, together with corresponding changes in hepcidin and ferroportin expressions, only DFO showed a protective effect against liver injury despite relatively small liver concentr

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Shock

  • ISSN

    1073-2322

  • e-ISSN

  • Volume of the periodical

    42

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    372-379

  • UT code for WoS article

    000342465100013

  • EID of the result in the Scopus database