Effect of GABA(B) receptor agonist SKF97541 on cortical and hippocampal epileptic afterdischarges
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24702499
DOI
10.33549/physiolres.932699
PII: 932699
Knihovny.cz E-resources
- MeSH
- GABA-B Receptor Agonists pharmacology MeSH
- Electroencephalography drug effects MeSH
- Epilepsy physiopathology MeSH
- Hippocampus physiopathology MeSH
- Rats MeSH
- Cerebral Cortex physiopathology MeSH
- Organophosphorus Compounds pharmacology MeSH
- Rats, Wistar MeSH
- Pyramidal Cells drug effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 3-aminopropyl(methyl)phosphinic acid MeSH Browser
- GABA-B Receptor Agonists MeSH
- Organophosphorus Compounds MeSH
Activation of GABA(B) receptors leads to longer inhibitory postsynaptic potentials than activation of GABA(A) receptors. Therefore GABA(B) receptors may be a target for anticonvulsant therapy. The present study examined possible effects of GABA(B) receptor agonist SKF97541 on cortical and hippocampal epileptic afterdischarges (ADs). Epileptic ADs elicited by electrical stimulation of sensorimotor cortex or dorsal hippocampus were studied in adult male Wistar rats. Stimulation series were applied 6 times with 10- or 20-min interval. Either interval was efficient for reliable elicitation of cortical ADs but stimulation at 10-min intervals did not reliably elicit hippocampal ADs, many stimulations were without effect. SKF97541 in dose 1 mg/kg significantly prolonged cortical ADs. Duration of hippocampal ADs was not significantly changed by either dose of SKF97541 in spite of a marked myorelaxant effect of the higher dose. Our present data demonstrated that neither cortical nor hippocampal ADs in adult rats were suppressed by GABA(B) receptor agonist SKF97541. Proconvulsant effect on cortical ADs indicates a different role in these two brain structures. In addition, duration of refractory period for electrically-induced ADs in these two structures in adult rats is different.
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