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Impairment of mitochondrial function of rat hepatocytes by high fat diet and oxidative stress

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F14%3A10271880" target="_blank" >RIV/00216208:11150/14:10271880 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985823:_____/14:00428971

  • Result on the web

    <a href="http://www.biomed.cas.cz/physiolres/pdf/63/63_271.pdf" target="_blank" >http://www.biomed.cas.cz/physiolres/pdf/63/63_271.pdf</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Impairment of mitochondrial function of rat hepatocytes by high fat diet and oxidative stress

  • Original language description

    Fatty liver disease associated with obesity is an important medical problem and the mechanisms for lipid accumulation in hepatocytes are not fully elucidated yet. Recent findings indicate that mitochondria play an important role in this process. Our dataon hepatocytes in which mitochondria are in contact with other cytosolic structures important for their function, extend observations obtained on isolated mitochondria and confirm inhibition of Complex I activity in hepatocytes isolated from rats fed byhigh fat diet (HFD) compared with controls fed by standard diet (STD). Furthermore we have found that HFD hepatocytes are more sensitive to the peroxidative stress because under these conditions also Complex II activity is disturbed. Therefore in HFD animals decrease of Complex I activity cannot be compensated by Complex II substrates as in STD hepatocytes. Our data indicate that combination of HFD and peroxidative stress potentiates HFD damaging effect of mitochondria because both bran

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    ED - Physiology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/LL1204" target="_blank" >LL1204: Genetic analysis of mitochondrial proteome: Integration of mitochondrial-nuclear epistasis with disease phenotypes in the rat</a><br>

  • 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

    Physiological Research

  • ISSN

    0862-8408

  • e-ISSN

  • Volume of the periodical

    63

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    4

  • Pages from-to

    271-274

  • UT code for WoS article

    000336459800016

  • EID of the result in the Scopus database