Status epilepticus in immature rats leads to behavioural and cognitive impairment and epileptogenesis
Jazyk angličtina Země Francie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
15217382
DOI
10.1111/j.0953-816x.2004.03410.x
PII: EJN3410
Knihovny.cz E-zdroje
- MeSH
- bludiště - učení fyziologie MeSH
- chování zvířat fyziologie MeSH
- elektroencefalografie MeSH
- kognitivní poruchy etiologie patofyziologie MeSH
- krysa rodu Rattus MeSH
- mozek patofyziologie MeSH
- pilokarpin toxicita MeSH
- pohybová aktivita fyziologie MeSH
- potkani Wistar MeSH
- status epilepticus chemicky indukované komplikace MeSH
- tělesná hmotnost fyziologie MeSH
- věkové faktory MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- pilokarpin MeSH
It remains under dispute whether status epilepticus (SE) in the perinatal period or early childhood or the underlying neuropathology is the cause of functional impairment later in life. The present study examined whether SE induced by LiCl-pilocarpine in normal immature brain (at the age of 12 or 25 days; P12 or P25) causes cognitive decline and epileptogenesis, and the data were compared to those of rats undergoing SE as adults. Rats in the P12 group had impaired memory (repeated exposure to open-field paradigm) and emotional behaviour (lower proportion of open-arm entries and higher incidence of risk assessment period in elevated plus-maze) when assessed 3 months after SE, although not as severe as in the older age groups. Importantly, video-electroencephalography monitoring 3 months after SE demonstrated that 25% of rats in the P12 and 50% in P25 group developed spontaneous seizures. Only nonconvulsive seizures (ictal activity in hippocampus accompanied by automatisms) were recorded in the P12 group whereas rats in the P25 group exhibited clonic convulsions. The present findings indicate that SE is harmful to the immature brain as early as P12, which might be compared with early infancy in humans.
Citace poskytuje Crossref.org
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