Rebound increase in seizure susceptibility but not isolation-induced calls after single administration of clonazepam and Ro 19-8022 in infant rats
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21130691
DOI
10.1016/j.yebeh.2010.10.021
PII: S1525-5050(10)00668-2
Knihovny.cz E-zdroje
- MeSH
- analýza rozptylu MeSH
- chinoliziny farmakologie MeSH
- GABA modulátory farmakologie MeSH
- klonazepam farmakologie MeSH
- krysa rodu Rattus MeSH
- náchylnost k nemoci chemicky indukované MeSH
- novorozená zvířata MeSH
- pentylentetrazol MeSH
- pohybová aktivita účinky léků MeSH
- potkani Wistar MeSH
- pyrrolidiny farmakologie MeSH
- receptory GABA-A metabolismus MeSH
- vokalizace zvířat účinky léků MeSH
- záchvaty chemicky indukované metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chinoliziny MeSH
- GABA modulátory MeSH
- klonazepam MeSH
- pentylentetrazol MeSH
- pyrrolidiny MeSH
- receptory GABA-A MeSH
- Ro 19-8022 MeSH Prohlížeč
The purpose of our study was to determine whether a single administration of anticonvulsant doses of two ligands of benzodiazepine receptors, clonazepam and Ro 19-8022, leads to development of rebound phenomena in immature 12-day-old rats. Three tests were used: pentylenetetrazole (PTZ)-induced seizures, isolation-induced ultrasonic vocalizations, and motor performance. Susceptibility to the convulsant effects of PTZ decreased 24 hours, but increased 48 hours, after clonazepam administration. Ultrasonic vocalizations were completely suppressed 30 minutes and 3 hours after clonazepam; a moderate inhibitory effect persisted even at 48 hours. Motor abilities were slightly compromised up to 3 hours. Similar effects of Ro 19-8022 on PTZ-induced seizures and ultrasonic vocalizations were observed 24 and 48 hours after administration; motor performance was not affected. Rebound proconvulsant effects followed different time courses after administration of the two benzodiazepine receptor ligands in developing animals. Anxiolytic-like effects of these drugs were still present at the time when animals exhibited rebound proconvulsant effects.
Epilepsy Behav. 2012 Mar;23(3):398 PubMed
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