Enhanced extinction of cocaine seeking in brain-derived neurotrophic factor Val66Met knock-in mice. Academic Article uri icon

Overview

abstract

  • The Val66Met polymorphism in the brain-derived neurotropic factor (BDNF) gene results in alterations in fear extinction behavior in both human populations and mouse models. However, it is not clear whether this polymorphism plays a similar role in extinction of appetitive behaviors. Therefore, we examined operant learning and extinction of both food and cocaine self-administration behavior in an inbred genetic knock-in mouse strain expressing the variant Bdnf. These mice provide a unique opportunity to relate alterations in aversive and appetitive extinction learning as well as provide insight into how human genetic variation can lead to differences in behavior. BDNF(Met/Met) mice exhibited a severe deficit in operant learning as demonstrated by an inability to learn the food self-administration task. Therefore, extinction experiments were performed comparing wildtype (BDNF(Val/Val) ) animals to mice heterozygous for the Met allele (BDNF(Val/Met) ), which did not differ in food or cocaine self-administration behavior. In contrast to the deficit in fear extinction previously demonstrated in these mice, we found that BDNF(Val/Met) mice exhibited more rapid extinction of cocaine responding compared to wildtype mice. No differences were found between the genotypes in the extinction of food self-administration behavior or the reinstatement of cocaine seeking, indicating that the effect is specific to extinction of cocaine responding. These results suggest that the molecular mechanisms underlying aversive and appetitive extinction are distinct from one another and BDNF may play opposing roles in the two phenomena.

publication date

  • March 7, 2012

Research

keywords

  • Brain-Derived Neurotrophic Factor
  • Cocaine-Related Disorders
  • Drug-Seeking Behavior
  • Extinction, Psychological

Identity

PubMed Central ID

  • PMC3626276

Scopus Document Identifier

  • 84858862139

Digital Object Identifier (DOI)

  • 10.1111/j.1460-9568.2012.08021.x

PubMed ID

  • 22394056

Additional Document Info

volume

  • 35

issue

  • 6