Time course of neuronal damage in the hippocampus following lithium-pilocarpine status epilepticus in 12-day-old rats
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20673826
DOI
10.1016/j.brainres.2010.07.072
PII: S0006-8993(10)01662-8
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- chlorid lithný toxicita MeSH
- degenerace nervu chemicky indukované patologie MeSH
- gyrus dentatus účinky léků patologie MeSH
- hipokampus účinky léků patologie MeSH
- krysa rodu Rattus MeSH
- modely nemocí na zvířatech MeSH
- novorozená zvířata MeSH
- pilokarpin farmakologie MeSH
- potkani Wistar MeSH
- pyramidové buňky účinky léků metabolismus patologie MeSH
- status epilepticus chemicky indukované patologie 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
- chlorid lithný MeSH
- pilokarpin MeSH
Status epilepticus (SE) leads to serious damage in hippocampus of the adult brain. Much less is known about immature brain where neuronal degeneration may have different localization and time course. Lithium-pilocarpine SE was induced in 12-day-old male Wistar rats. Six different intervals after SE (from 4 h to 1 week) were studied using Fluoro-Jade B staining. Three to four animals were used for every interval. Severity of damage in individual parts of hippocampal formation was semi-quantified. A consistent neuronal damage occurred in all hippocampal fields (CA 1, CA 3, dentate gyrus) at all survival intervals. Hippocampal fields CA 1 and CA 3 exhibited degeneration of interneurons located mainly in stratum oriens and pyramidale at shorter intervals (4-12h). Massive degeneration of pyramidal cells started at 24h in CA 1 and at 48 h in CA 3. Dentate gyrus exhibited degenerating neurons in granular layer with a peak at short intervals (4-8 h), and molecular layer was spared. The lower blade of dentate gyrus was more affected than the upper blade. Damage of hilar neurons was negligible. Our results demonstrate that SE elicited in immature rats causes acute neurodegeneration in the hippocampus. Time course of this degeneration is different for individual parts of hippocampal formation and for individual cell types.
Citace poskytuje Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague
The outcome of early life status epilepticus-lessons from laboratory animals