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Multidrug and toxin extrusion proteins (MATE/SLC47); role in pharmacokinetics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F13%3A10145940" target="_blank" >RIV/00216208:11160/13:10145940 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S1357272513002069" target="_blank" >http://www.sciencedirect.com/science/article/pii/S1357272513002069</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.biocel.2013.06.022" target="_blank" >10.1016/j.biocel.2013.06.022</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multidrug and toxin extrusion proteins (MATE/SLC47); role in pharmacokinetics

  • Original language description

    Mammal multidrug and toxin extrusion protein 1 (MATE 1) encoded by SLC47A1 gene was described in 2005 as an efflux transporter that mediates proton-coupled organic cation secretion. In the kidney and liver, MATEs work in concert with organic cation transporters (OCTs), together representing an eliminatory pathway for organic cations. Over 40 clinically used drugs and several endogenous compounds are known substrates or inhibitors of MATEs. These transporters are supposed to modulate pharmacokinetics/toxicokinetics and to play a role in drug resistance and (patho)physiological processes. Drug drug interactions on MATE transporters and polymorphisms in SLC47A genes may affect renal excretion of substrate drugs. Expression and function of MATEs in tissuesother than kidney and liver remain to be elucidated.

  • 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/GAP303%2F12%2F0850" target="_blank" >GAP303/12/0850: Transplacental pharmacokinetics of antiretroviral drugs; interactions with drug-efflux transporters</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    International Journal of Biochemistry and Cell Biology

  • ISSN

    1357-2725

  • e-ISSN

  • Volume of the periodical

    45

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    5

  • Pages from-to

    2007-2011

  • UT code for WoS article

    000324605300006

  • EID of the result in the Scopus database