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Electrographic seizures induced by activation of ET A and ET B receptors following intrahippocampal infusion of endothelin-1 in immature rats occur by different mechanisms

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F20%3A43920486" target="_blank" >RIV/00023752:_____/20:43920486 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985823:_____/20:00524259 RIV/00216208:11310/20:10414744

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0014488620300868?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0014488620300868?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.expneurol.2020.113255" target="_blank" >10.1016/j.expneurol.2020.113255</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electrographic seizures induced by activation of ET A and ET B receptors following intrahippocampal infusion of endothelin-1 in immature rats occur by different mechanisms

  • Original language description

    We have demonstrated previously that activation of either the ETA or ETB receptor can induce acute electrographic seizures following the intrahippocampal infusion of endothelin-1 (ET-1) in immature (P12) rats. We also demonstrated that activation of the ETA receptor is associated with marked focal ischemia, while activation of the ETB receptor is not. Exploring the mechanisms underlying seizures induced by these two ET-1 receptor interactions can potentially provide insight into how focal ischemia in immature animals produces seizures and whether ischemiarelated seizures differ from seizures not associated with ischemia. To explore these seizure mechanisms we used microdialysis to determine biomarkers associated with seizures in P12 rats following the intrahippocampal infusion of two different agents: (1) ET-1, which activates both the ETA and ETB receptors and causes focal ischemia and (2) Ala-ET-1, which selectively activates only the ETB receptor and does not cause ischemia. Our results show that seizures associated with combined ETA and ETB receptor activation (and ischemia) have a different temporal distribution and microdialysis profile from seizures associated with ETB activation alone (and without ischemia). Seizures with combined activation peak within the first hour after infusion and the microdialysis profile is characterized by a significant increase in the ratio of glutamic acid to GABA. By contrast, seizures with activation of only the ETB receptor peak in the second hour after infusion and microdialysis shows a significant increase in the ratio of leukotriene B4 to prostaglandin E2. These findings suggest that ischemia-related seizures in immature animals involve an imbalance of excitation and inhibition, while non-ischemiarelated seizures involve an inflammatory process resulting from an excess of leukotrienes.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30210 - Clinical neurology

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)

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Experimental Neurology

  • ISSN

    0014-4886

  • e-ISSN

  • Volume of the periodical

    328

  • Issue of the periodical within the volume

    June

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    142

  • Pages from-to

    "Article Number: 113255"

  • UT code for WoS article

    000527888300009

  • EID of the result in the Scopus database

    2-s2.0-85080116749