Publication Date:
2002
abstract:
Acquisition and storage of aversive memories is one of the basic
principles of central nervous systems throughout the animal kingdom. In
the absence of reinforcement, the resulting behavioural response will
gradually diminish to be finally extinct. Despite the importance of
extinction, its cellular mechanisms are largely unknown. The cannabinoid
receptor 1 (CB1) and endocannabinoids are present in memory-related brain
areas and modulate memory. Here we show that the endogenous cannabinoid
system has a central function in extinction of aversive memories. CB1-
deficient mice showed strongly impaired short-term and long-term
extinction in auditory fear-conditioning tests, with unaffected memory
acquisition and consolidation. Treatment of wild-type mice with the CB1
antagonist SR141716A mimicked the phenotype of CB1-deficient mice,
revealing that CB1 is required at the moment of memory extinction.
Consistently, tone presentation during extinction trials resulted in
elevated levels of endocannabinoids in the basolateral amygdala complex,
a region known to control extinction of aversive memories. In the
basolateral amygdala, endocannabinoids and CB1 were crucially involved in
long-term depression of GABA (gamma-aminobutyric acid)-mediated
inhibitory currents. We propose that endocannabinoids facilitate
extinction of aversive memories through their selective inhibitory
effects on local inhibitory networks in the amygdala.
Iris type:
01.01 Articolo in rivista
Keywords:
memoria; endocannabinoidi; fobia
List of contributors: