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Access of inhibitory neurosteroids to the NMDA receptor

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F12%3A33143002" target="_blank" >RIV/61989592:15310/12:33143002 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985823:_____/12:00379112 RIV/61388963:_____/12:00379112

  • Result on the web

    <a href="http://onlinelibrary.wiley.com/doi/10.1111/j.1476-5381.2011.01816.x/abstract;jsessionid=AC688D0796D6A68D8D0E67DA50B1D2A7.d04t03" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1111/j.1476-5381.2011.01816.x/abstract;jsessionid=AC688D0796D6A68D8D0E67DA50B1D2A7.d04t03</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/j.1476-5381.2011.01816.x" target="_blank" >10.1111/j.1476-5381.2011.01816.x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Access of inhibitory neurosteroids to the NMDA receptor

  • Original language description

    BACKGROUND AND PURPOSE NMDA receptors are glutamatergic ionotropic receptors involved in excitatory neurotransmission, synaptic plasticity and excitotoxic cell death. Many allosteric modulators can influence the activity of these receptors positively ornegatively, with behavioural consequences. 20-Oxo-5 beta-pregnan-3a-yl sulphate (pregnanolone sulphate; PA-6) is an endogenous neurosteroid that inhibits NMDA receptors and is neuroprotective. We tested the hypothesis that the interaction of PA-6 with the plasma membrane is critical for its inhibitory effect at NMDA receptors. EXPERIMENTAL APPROACH Electrophysiological recordings and live microscopy were performed on heterologous HEK293 cells expressing GluN1/GluN2B receptors and cultured rat hippocampal neurons. KEY RESULTS Our experiments showed that the kinetics of the steroid inhibition were slow and not typical of drug-receptor interaction in an aqueous solution. In addition, the recovery from steroid inhibition was accelerated by

  • 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

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    British Journal of Pharmacology

  • ISSN

    0007-1188

  • e-ISSN

  • Volume of the periodical

    166

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    15

  • Pages from-to

    1069-1083

  • UT code for WoS article

    000303923000021

  • EID of the result in the Scopus database