Changes of cortical interhemispheric responses after status epilepticus in immature rats
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
15987250
DOI
10.1111/j.1528-1167.2005.01004.x
PII: EPI01004
Knihovny.cz E-resources
- MeSH
- Lithium Chloride pharmacology MeSH
- Corpus Callosum drug effects pathology physiopathology MeSH
- Nerve Degeneration chemically induced pathology physiopathology MeSH
- Electric Stimulation MeSH
- Fluoresceins MeSH
- Fluorescent Dyes MeSH
- Functional Laterality drug effects physiology MeSH
- Interneurons metabolism pathology MeSH
- Rats MeSH
- Cerebral Cortex drug effects pathology physiopathology MeSH
- Organic Chemicals MeSH
- Pilocarpine pharmacology MeSH
- Rats, Wistar MeSH
- Status Epilepticus chemically induced pathology physiopathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Lithium Chloride MeSH
- Fluoresceins MeSH
- Fluorescent Dyes MeSH
- fluoro jade MeSH Browser
- Organic Chemicals MeSH
- Pilocarpine MeSH
PURPOSE: To study cortical excitability after status epilepticus induced in two age groups of immature rats. METHODS: Lithium-pilocarpine status epilepticus was elicited in 12- (SE12) or 25-day-old (SE25) rats. Control siblings received saline instead of pilocarpine. Interhemispheric responses were elicited by stimulation of sensorimotor region of cerebral cortex 3, 6, 9, 13, or 26 days after status. Single biphasic pulses with intensities from 0.2 to 4 mA were used for stimulation; eight responses were always averaged. Amplitude of the first positive and negative waves (i.e., monosynaptic transcallosal responses) was measured and used for construction of input-output (I/O) curves. FluoroJade B was used to visualize degenerating neurons 24 h after status in both age groups. RESULTS: No significant changes were found at short intervals, but only a tendency to lower amplitudes 3 days after status in SE12 group. Marked changes appeared 26 days after status. The younger group exhibited lower amplitudes than did control rats, whereas SE25 animals generated responses with higher amplitude than did controls (i.e., the I/O curve was steeper. FluoroJade B-positive neurons were scarce in SE12 rats, whereas a substantial number of positive neurons was found in SE25 animals. The positive neurons exhibited characteristics of interneurons, and their distribution in cortical layers differed in the two groups. CONCLUSIONS: Status epilepticus resulted in neuronal death in both SE12 and SE25 animals. Changes in transcallosal evoked potentials were opposite in the two age groups. Augmented amplitude of responses in SE25 rats may indicate an increased cortical excitability.
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