Anticonvulsant and behavioral effects of muscimol in immature rats
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25084038
DOI
10.1016/j.brainres.2014.07.038
PII: S0006-8993(14)00989-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cortical afterdischarges, Motor activities, Muscimol, Ontogeny, Pentetrazol-induced seizures, Rat,
- MeSH
- agonisté receptorů GABA-A farmakologie MeSH
- antikonvulziva farmakologie MeSH
- elektroencefalografie MeSH
- epilepsie farmakoterapie patofyziologie MeSH
- modely nemocí na zvířatech MeSH
- mozek účinky léků růst a vývoj patofyziologie MeSH
- muscimol farmakologie MeSH
- neuropsychologické testy MeSH
- pátrací chování účinky léků fyziologie MeSH
- pentylentetrazol MeSH
- pohybová aktivita účinky léků fyziologie MeSH
- potkani Wistar MeSH
- stupeň závažnosti nemoci MeSH
- věkové faktory MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- záchvaty farmakoterapie patofyziologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- agonisté receptorů GABA-A MeSH
- antikonvulziva MeSH
- muscimol MeSH
- pentylentetrazol MeSH
Potentiation of GABAergic inhibition is a mechanism of action of many antiepileptic drugs. The potential use of an agonist of GABAA receptors, muscimol, as an antiepileptic drug was studied in immature rats by assessing anticonvulsant activity and side effects on motor activities. Anticonvulsant action was tested in two models of seizures (pentetrazol-induced convulsions and cortical epileptic afterdischarges). Off target effect on motor performance was assessed in a battery of tests and in the open field in three age groups (12-, 18- and 25-day-old rats). Muscimol was administered in doses from 0.1 to 1mg/kg i.p. Only the 1 mg/kg dose exhibited marked anticonvulsant effect against pentetrazol-induced convulsions in 12- and 18-day-old rats, proconvulsant effect was observed in the second model in 18- and 25-day-old rats as prolongation of afterdischarges. Even the 0.5 mg/kg dose suppressed spontaneous locomotion and heavily compromised motor performance. The effect on motor activity was marked in the youngest group and decreased with age. Due to the low anticonvulsant potency and serious side effects, systemic administration of a competitive agonist of GABAA receptors in immature animals is not a promising strategy for new anticonvulsants.
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