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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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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