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Autoradiographic imaging and quantification of the high-affinity GHB binding sites in rodent brain using H-3-HOCPCA

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F16%3A00469234" target="_blank" >RIV/61388963:_____/16:00469234 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.neuint.2016.09.002" target="_blank" >http://dx.doi.org/10.1016/j.neuint.2016.09.002</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.neuint.2016.09.002" target="_blank" >10.1016/j.neuint.2016.09.002</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Autoradiographic imaging and quantification of the high-affinity GHB binding sites in rodent brain using H-3-HOCPCA

  • Original language description

    GHB (gamma-hydroxybutyric acid) is a compound endogenous to mammalian brain with high structural resemblance to GABA. GHB possesses nanomolar-micromolar affinity for a unique population of binding sites, but the exact nature of these remains elusive. In this study we utilized the highly selective GHB analogue, 3-hydroxycyclopent-1-enecarboxylic acid (HOCPCA) as a tritiated version (H-3-HOCPCA) to radioactively label the specific GHB high-affinity binding site and gain further insight into the density, distribution and developmental profile of this protein. We show that, in low nanomolar concentrations, 3H-HOCPCA displays excellent signal-to-noise ratios using rodent brain autoradiography, which makes it a valuable ligand for anatomical quantification of native GHB binding site levels. Our data confirmed that 3H-HOCPCA labels only the high-affinity specific GHB binding site, found in high density in cortical and hippocampal regions. The experiments revealed markedly stronger binding at pH 6.0 (K-d 73.8 nM) compared to pH 7.4 (Kd 2312 nM), as previously reported for other GHB radioligands but similar B-max values. Using H-3-HOCPCA we analyzed the GHB binding protein profile during mouse brain development. Due to the high sensitivity of this radioligand, we were able to detect low levels of specific binding already at E15 in mouse brain, which increased progressively until adulthood. Collectively, we show that H-3-HOCPCA is a highly sensitive radioligand, offering advantages over the commonly used radioligand H-3-NCS-382, and thus a very suitable in vitro tool for qualitative and quantitative autoradiography of the GHB high-affinity site.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Neurochemistry International

  • ISSN

    0197-0186

  • e-ISSN

  • Volume of the periodical

    100

  • Issue of the periodical within the volume

    Nov

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    138-145

  • UT code for WoS article

    000388780300016

  • EID of the result in the Scopus database

    2-s2.0-84988521805