Abnormal fear response and aggressive behavior in mutant mice deficient for alpha-calcium-calmodulin kinase II

Science. 1994 Oct 14;266(5183):291-4. doi: 10.1126/science.7939668.

Abstract

Mice deficient for the gene encoding alpha-calcium-calmodulin-dependent kinase II (alpha-CaMKII knockout mice) provide a promising tool to link behavioral and cellular abnormalities with a specific molecular lesion. The heterozygous mouse exhibited a well-circumscribed syndrome of behavioral abnormalities, consisting primarily of a decreased fear response and an increase in defensive aggression, in the absence of any measured cognitive deficits. Unlike the heterozygote, the homozygote displayed abnormal behavior in all paradigms tested. At the cellular level, both extracellular and whole-cell patch clamp recordings indicated that serotonin release in putative serotonergic neurons of the dorsal raphe was reduced. Thus, alpha-CaMKII knockout mice, in particular the heterozygote, may provide a model for studying the molecular and cellular basis underlying emotional disorders involving fear and aggression.

Publication types

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

MeSH terms

  • Aggression*
  • Animals
  • Behavior, Animal
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases / deficiency
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / physiology*
  • Fear*
  • Fluoxetine / pharmacology
  • Gene Dosage
  • Heterozygote
  • Homozygote
  • In Vitro Techniques
  • Membrane Potentials
  • Mice
  • Mice, Knockout
  • Mutation
  • Neurons / metabolism
  • Patch-Clamp Techniques
  • Raphe Nuclei / metabolism
  • Serotonin / metabolism
  • Serotonin / pharmacology
  • Synaptic Transmission / drug effects

Substances

  • Fluoxetine
  • Serotonin
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Camk2a protein, mouse