(K141934) Támogató: Hungarian National Research, Development and Innovation Office
(K138763) Támogató: NKFIH
(K120311) Támogató: NKFIH
(TKP2021-EGA-16)
The extinction of conditioned fear is frequently used in laboratories as a model for
human exposure therapy and is crucial for studies of posttraumatic stress disorder
(PTSD). However, the efficacy of specific protocols can vary greatly, and the underlying
brain mechanisms are not sufficiently clarified. To address this issue, variable starting
time (one or twenty-eight days after fear conditioning) and extinction protocols were
used, and the efficacy and durability of fear extinction were also studied. Changes
in the behavior, stress hormone levels and neuronal activation patterns of stressed
rats were analyzed. Conditioned fear was rapidly and efficiently extinguished by all
the protocols investigated. However, when these extinction protocols were initiated
one day after fear training, conditioned fear relapsed spontaneously four weeks later.
In contrast, when extinction trials were started 28 days after conditioning, no relapse
occurred. Hormone measurements taken by the end of extinction trials indicated that
adrenocorticotropin, but not corticosterone responses reflected behavioral extinction
without any sign of relapse. The last extinction training increased the activation
of the medial prefrontal cortex and decreased the activation of the central and medial
amygdala when extinction began one day after fear conditioning. By contrast, the activation
of the basolateral amygdala and the entire hippocampus decreased by the last training
session when extinction started 28 days after fear conditioning. Our findings show
that extinction training can extinguish remote fear memories more effectively than
recent ones, and that the brain mechanisms underlying remote and recent fear memory
extinction differ. Laboratory models should also focus on a later time point to increase
their translational value.