Degenerative neuronal changes in the rat thalamus induced by status epilepticus at different developmental stages
Language English Country Netherlands Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15716027
DOI
10.1016/j.eplepsyres.2004.11.001
PII: S0920-1211(04)00237-2
Knihovny.cz E-resources
- MeSH
- Staining and Labeling MeSH
- Time Factors MeSH
- Behavior, Animal MeSH
- Nerve Degeneration complications pathology MeSH
- Computer-Aided Design MeSH
- Fluoresceins MeSH
- Fluorescent Dyes metabolism MeSH
- Rats MeSH
- Neurons metabolism pathology MeSH
- Animals, Newborn growth & development MeSH
- Organic Chemicals MeSH
- Cell Count methods MeSH
- Rats, Wistar MeSH
- Status Epilepticus etiology pathology MeSH
- Thalamus pathology physiopathology MeSH
- Age Factors MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Fluoresceins MeSH
- Fluorescent Dyes MeSH
- fluoro jade MeSH Browser
- Organic Chemicals MeSH
SE was induced in Wistar rats at post-natal (P) days 12, 15, 18, 21, and 25 to determine distribution and severity of thalamic damage in relation to time after SE. Six different intervals from 4 h up to 1 week were studied using Fluoro-Jade B (FJB) staining. Severity of damage was semi-quantified for every age-and-interval group. Distribution of neuronal damage within various thalamic nuclei was mapped by a computer-aided digitizing system. A consistent neuronal damage occurred in functionally heterogenous thalamic nuclei. Damage was found in all age groups although its extension and time course as well as the number of involved thalamic nuclei varied. Number of injured thalamic nuclei rapidly increased with age on SE-onset. In P12 group, degenerating neurons were consistently seen in the mediodorsal and lateral dorsal thalamic nuclei. Since P15, neurodegeneration was observed additionally in midline, ventral and caudal thalamic nuclei (visual and auditory thalamic nuclei), in the lateral posterior and in the reticular nucleus. In P21 and P25 animals, the majority of thalamic nuclei exhibited marked neuronal damage. Nuclei with a small number (anterior and intralaminar) or no FJB-positive neurons (the ventral nucleus of the lateral geniculate body) were exceptional. The pattern of thalamic damage is age-specific; its extent and severity increases with age.
References provided by Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague