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Memory consolidation in both trace and delay fear conditioning is disrupted by intra-amygdala infusion of the protein synthesis inhibitor anisomycin
Author(s) -
Janine L. Kwapis,
Timothy J. Jarome,
Janet C. Schiff,
Fred J. Helmstetter
Publication year - 2011
Publication title -
learning and memory
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.228
H-Index - 136
eISSN - 1549-5485
pISSN - 1072-0502
DOI - 10.1101/lm.023945.111
Subject(s) - anisomycin , fear conditioning , amygdala , memory consolidation , basolateral amygdala , engram , psychology , conditioning , neuroscience , classical conditioning , stimulus (psychology) , protein biosynthesis , chemistry , cognitive psychology , hippocampus , biochemistry , statistics , mathematics
Memory for delay fear conditioning requires the synthesis of new mRNA and protein in the basolateral amygdala. It is currently unknown whether similar molecular processes in the amygdala are required for the formation of trace fear memory, in which a stimulus-free interval is inserted between the conditional stimulus (CS) and unconditional stimulus (UCS). Here, we show that infusion of the protein synthesis inhibitor anisomycin into the basolateral amygdala disrupts consolidation of both trace and delay fear conditioning. This is the first evidence that protein synthesis in the amygdala is necessary for the formation of both trace and delay fear memory.

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