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The Journal of Neuroscience, September 15, 2002, 22(18):7892-7902
Regulation of Synaptic Plasticity Genes during Consolidation of
Fear Conditioning
Kerry J.
Ressler,
Gayla
Paschall,
Xiao-liu
Zhou, and
Michael
Davis
Department of Psychiatry and Behavioral Sciences, Center for
Behavioral Neuroscience, Emory University School of Medicine, Atlanta,
Georgia 30322
In mammals, long-term memory induced by Pavlovian fear conditioning
has been shown to be dependent on the amygdala during a protein and
mRNA synthesis-dependent phase of memory consolidation. We have used
genes identified in a kainic acid model of synaptic plasticity as
in situ hybridization probes during the consolidation period after fear conditioning. We found that these genes were transcriptionally regulated in several brain areas only when stimuli were presented in a manner that supported behavioral learning and not
after unpaired presentations or footshocks alone. Immediate early genes
and neurofilament mRNA peaked ~30 min after conditioning, as
expected. Interestingly, nurr-1, -actinin, and 16c8
increased ~2-4 hr later, whereas neurogranin and gephyrin decreased
during that time. Our results suggest that fear memory consolidation occurs within a broad neural circuit that includes, but is not limited
to, the amygdala. Together, a broad array of transcriptionally regulated genes, encoding transcription factors, cytoskeletal proteins,
adhesion molecules, and receptor stabilization molecules, appear to
mediate the neural plasticity underlying specific forms of long-term
memory in mammals.
Key words:
fear conditioning; learning; consolidation; synaptic
plasticity; startle; amygdala
Copyright © 2002 Society for Neuroscience 0270-6474/02/22187892-11$05.00/0
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