GABAB, not GABAA receptors play a role in cortical postictal refractoriness
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
LH11015
PHS HHS - United States
PubMed
25229720
DOI
10.1016/j.neuropharm.2014.09.007
PII: S0028-3908(14)00314-1
Knihovny.cz E-zdroje
- Klíčová slova
- Bicuculline (PubChem CID 102037), CGP35348 (PubChem CID 107699), Cortical seizures, GABA receptors antagonists, Pentylentetrazol (PubChem CID 5917), Picrotoxin (PubChem CID 31304), Postictal refractoriness, Rat, Ro 19-4603 (PubChem CID 127382),
- MeSH
- antagonisté receptorů GABA-A farmakologie MeSH
- antagonisté receptorů GABA-B farmakologie MeSH
- azepiny farmakologie MeSH
- bikukulin farmakologie MeSH
- elektrická stimulace MeSH
- epilepsie farmakoterapie patofyziologie MeSH
- implantované elektrody MeSH
- mozková kůra účinky léků patofyziologie MeSH
- organofosforové sloučeniny farmakologie MeSH
- pentylentetrazol farmakologie MeSH
- pikrotoxin farmakologie MeSH
- potkani Wistar MeSH
- receptory GABA-A metabolismus MeSH
- receptory GABA-B metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- antagonisté receptorů GABA-A MeSH
- antagonisté receptorů GABA-B MeSH
- azepiny MeSH
- bikukulin MeSH
- CGP 35348 MeSH Prohlížeč
- organofosforové sloučeniny MeSH
- pentylentetrazol MeSH
- pikrotoxin MeSH
- receptory GABA-A MeSH
- receptory GABA-B MeSH
- Ro 19-4603 MeSH Prohlížeč
Postictal refractoriness may be taken as an expression of lasting activity of inhibitory systems arresting seizures. We tested drugs interfering with GABAergic inhibitory system in pairs of cortical epileptic afterdischarges induced with 1-min interval in rats. Under control conditions the second stimulation failed to elicit an afterdischarge. This postictal refractoriness was not affected by antagonists of GABAA receptors acting at three binding sites (bicuculline, picrotoxin, benzodiazepine inverse agonist Ro 19-4603) as well as by a less specific antagonist pentetrazol. In contrast, antagonist of GABAB receptors CGP35348 partially blocked the refractoriness. Cooperation of different inhibitory systems is probably necessary to abolish postictal refractoriness in neocortex. This article is part of the Special Issue entitled 'GABAergic Signaling in Health and Disease'.
Citace poskytuje Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague