Different effects of nonNMDA and NMDA receptor antagonists (NBQX and dizocilpine) on cortical epileptic afterdischarges in rats
Language English Country Netherlands Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17070784
DOI
10.1016/j.brainres.2006.09.072
PII: S0006-8993(06)02849-6
Knihovny.cz E-resources
- MeSH
- Excitatory Amino Acid Antagonists MeSH
- Quinoxalines administration & dosage MeSH
- Dizocilpine Maleate administration & dosage MeSH
- Electric Stimulation adverse effects MeSH
- Electroencephalography methods MeSH
- Epilepsy etiology pathology physiopathology prevention & control MeSH
- Evoked Potentials drug effects physiology radiation effects MeSH
- Rats MeSH
- Cerebral Cortex drug effects MeSH
- Rats, Wistar MeSH
- Dose-Response Relationship, Radiation MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline MeSH Browser
- Excitatory Amino Acid Antagonists MeSH
- Quinoxalines MeSH
- Dizocilpine Maleate MeSH
Excitatory amino acids play an important role in generation of epileptic seizures. To study the participation of different types of their receptors in cortical epileptic afterdischarges, a noncompetitive NMDA receptor antagonist dizocilpine and a competitive AMPA receptor antagonist NBQX were used. Adult rats with implanted epidural stimulation and registration electrodes were pretreated either with NBQX (30 or 60 mg/kg i.p.) or with dizocilpine (0.1 or 0.5 mg/kg i.p.) and low-frequency stimulation of sensorimotor cortical area was repeatedly applied with stepwise increased current intensities. Lower dose of NBQX unexpectedly decreased thresholds for elicitation of spike-and-wave afterdischarges (ADs), clonic seizures accompanying this type of ADs and for transition into the second, limbic type of ADs. Lower dose of dizocilpine increased these three thresholds. Higher doses of either drug did not significantly change threshold intensities. Duration of ADs was also influenced by the two antagonists in opposite directions: higher dose of NBQX resulted in prolongation of ADs mainly due to an increased duration of the spike-and-wave part of ADs whereas dizocilpine shortened ADs in a dose-dependent manner affecting both types of ADs. In addition, NBQX did not influence interhemispheric responses meanwhile dizocilpine moderately suppressed these evoked potentials. According to our results, NMDA receptors are important for generation of cortical epileptic afterdischarges meanwhile the role of AMPA receptors is not clear and has to be analyzed.
References provided by Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague