Activation of BDNF signaling prevents the return of fear in female mice

被引:87
作者
Baker-Andresen, Danay [1 ]
Flavell, Charlotte R. [1 ]
Li, Xiang [1 ]
Bredy, Timothy W. [1 ]
机构
[1] Univ Queensland, Queensland Brain Inst, Psychiat Epigenom Lab, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
SYNAPTIC PLASTICITY; PREFRONTAL CORTEX; SEX-DIFFERENCES; TRKB AGONIST; EXTINCTION; MEMORY; 7,8-DIHYDROXYFLAVONE; RECONSOLIDATION; ATTENUATION; AMYGDALA;
D O I
10.1101/lm.029520.112
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:237 / 240
页数:4
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