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[Cyclic AMP responsive element- and activator protein 1 DNA-binding activities in epilepsy model mice]
1Department of Pharmacology, College of Pharmacy, Nihon University, Funabashi, Japan.
Summary
Convulsive seizures significantly increase activator protein-1 (AP-1) and cyclic AMP responsive element (CRE) binding activities in the brain's cortex and hippocampus. These changes are specific to seizure type and brain region.
Area of Science:
- Neuroscience
- Molecular Biology
- Epilepsy Research
Context:
- Convulsive seizures are known to activate transcription factors like AP-1 in the brain.
- Previous studies indicated elevated AP-1 binding in absence seizures.
- The specific brain regions and transcription factors involved in convulsive seizures require further characterization.
Purpose:
- To investigate the correlation between convulsive seizures and inducible transcription factors.
- To determine the regional changes in AP-1 and CRE DNA-binding activities following different types of seizures.
- To differentiate the molecular responses to convulsive versus absence seizures.
Summary:
- Convulsive seizures induced by pentylentetrazole, kainic acid, and maximal electric shock (MES) increased AP-1 and CRE DNA-binding activities in the cerebral cortex and hippocampus.
- These increases were not observed in other brain regions.
- The anticonvulsant sodium phenobarbital suppressed both MES-induced seizures and the associated increases in DNA-binding activities, while ethosuximide did not.
- These findings suggest that convulsive seizures specifically enhance AP-1 and CRE binding in the cortex and hippocampus.
Impact:
- The study highlights regional differences in transcription factor activation between convulsive and absence seizures.
- This suggests distinct neural pathways are involved in the generation and spread of different seizure types.
- Provides insights into the molecular mechanisms underlying seizure-induced brain activity.