Fyn tyrosine kinase is required for normal amygdala kindling

Epilepsy Res. 1995 Oct;22(2):107-14. doi: 10.1016/0920-1211(95)00029-1.

Abstract

To identify specific genes involved with epileptogenesis kindling was examined in mice carrying mutations engineered by gene targeting. Amygdala kindling was tested in mice with a null-mutation in the Fyn tyrosine kinase gene, a mutation that raises the threshold for the induction of long-term potentiation in the hippocampus. The fyn mutants had a normal threshold, duration and stability of epileptiform after-discharge, which is crucial for kindling. Despite the normal after-discharge, fyn mutants showed a striking retardation in the rate of kindling. Once the kindled state was established in fyn mutants it remained stable. This implicates a Fyn-dependent biochemical pathway in the induction but not the maintenance of normal amygdala kindling. fyn is the first gene identified to be required for normal epileptogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amygdala / enzymology*
  • Amygdala / physiopathology
  • Animals
  • Behavior, Animal / physiology
  • Cells, Cultured
  • Epilepsy / enzymology
  • Epilepsy / etiology*
  • Epilepsy / genetics*
  • Female
  • Kindling, Neurologic / physiology*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mice, Mutant Strains
  • Mutation
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / physiology*

Substances

  • Protein-Tyrosine Kinases