Activation of BDNF signaling prevents the return of fear in female mice
Author(s) -
Danay BakerAndresen,
Charlotte R. Flavell,
Xiang Li,
Timothy W. Bredy
Publication year - 2013
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.029520.112
Subject(s) - extinction (optical mineralogy) , psychology , fear conditioning , anxiety , prefrontal cortex , hippocampus , neuroscience , endocrinology , medicine , cognition , psychiatry , biology , paleontology
There are significant sex differences in vulnerability to develop fear-related anxiety disorders. Females exhibit twice the rate of post-traumatic stress disorder (PTSD) as males and sex differences have been observed in fear extinction learning in both humans and rodents, with a failure to inhibit fear emerging as a precipitating factor in the development of PTSD. Here we report that female mice are resistant to fear extinction, and exhibit increased DNA methylation of Bdnf exon IV and a concomitant decrease in mRNA expression within the medial prefrontal cortex. Activation of BDNF signaling by the trkB agonist 7,8-dihydroxyflavone blocks the return of fear in female mice after extinction training, and thus represents a novel approach to treating fear-related anxiety disorders that are characterized by a resistance to extinction and increased propensity for renewal.
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