Characterization of the long-lasting activator protein-1 complex induced by kainic acid treatment

Brain Res. 1997 Oct 3;770(1-2):53-9. doi: 10.1016/s0006-8993(97)00744-0.

Abstract

Kainic acid is known to induce seizures, neuronal damage and cell loss in the rat hippocampus. Our laboratory has shown that a single kainic acid injection elicits acute increases of activator protein-1 DNA-binding activity and this activity stays at an elevated level for 2 weeks after kainic acid injection. However, some pathological changes such as mossy fiber sprouting do not occur until 2-3 weeks after the kainic acid injection and the specific transcription factors regulating the long-term events after kainic acid treatment are not clear. To determine the involvement of activator protein-1 transcription factors in the long-term events after kainic acid treatment, gel mobility-shift and Western blot analyses were used. The results showed that two activator protein-1 complexes with different mobilities occur during the acute stage. However, only the faster-migrating complex as well as the 35-37-kDa fos-related antigen and Jun-D proteins were seen during the late stage. These results suggest that different activator protein-1 complexes exist at different stages after convulsions and that they regulate ensembles of different genes.

MeSH terms

  • Animals
  • Antibody Specificity
  • Blotting, Western
  • Excitatory Amino Acid Agonists*
  • Hippocampus / chemistry
  • Hippocampus / metabolism
  • Kainic Acid*
  • Male
  • Peptide Fragments / analysis
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Proto-Oncogene Proteins c-fos / analysis
  • Proto-Oncogene Proteins c-fos / metabolism
  • Proto-Oncogene Proteins c-jun / analysis
  • Proto-Oncogene Proteins c-jun / immunology
  • Proto-Oncogene Proteins c-jun / metabolism
  • Rats
  • Rats, Inbred F344
  • Seizures / chemically induced
  • Seizures / metabolism*
  • Time Factors
  • Transcription Factor AP-1 / analysis
  • Transcription Factor AP-1 / chemistry
  • Transcription Factor AP-1 / metabolism*

Substances

  • Excitatory Amino Acid Agonists
  • Peptide Fragments
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Transcription Factor AP-1
  • Kainic Acid