A Genetic Variant BDNF Polymorphism Alters Extinction Learning in Both Mouse and Human

被引:452
作者
Soliman, Fatima [1 ,2 ]
Glatt, Charles E. [2 ]
Bath, Kevin G. [2 ]
Levita, Liat [1 ,2 ]
Jones, Rebecca M. [1 ,2 ]
Pattwell, Siobhan S. [2 ]
Jing, Deqiang [2 ]
Tottenham, Nim [1 ,2 ]
Amso, Dima [1 ,2 ]
Somerville, Leah H. [1 ,2 ]
Voss, Henning U. [3 ]
Glover, Gary [4 ]
Ballon, Douglas J. [3 ]
Liston, Conor [1 ,2 ]
Teslovich, Theresa [1 ,2 ]
Van Kempen, Tracey [1 ,2 ]
Lee, Francis S. [2 ]
Casey, B. J. [1 ,2 ]
机构
[1] Weill Cornell Med Coll, Sackler Inst Dev Psychobiol, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Psychiat, New York, NY 10065 USA
[3] Weill Cornell Med Coll, Citigrp Biomed Imaging Ctr, Dept Radiol, New York, NY 10065 USA
[4] Stanford Univ, Lucas Ctr Imaging, Dept Radiol, Stanford, CA 94305 USA
关键词
POSTTRAUMATIC-STRESS-DISORDER; VAL66MET POLYMORPHISM; NEUROTROPHIC FACTOR; PREFRONTAL CORTEX; FEAR EXTINCTION; CONDITIONED FEAR; HUMAN-MEMORY; AMYGDALA; ANXIETY; RECALL;
D O I
10.1126/science.1181886
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mouse models are useful for studying genes involved in behavior, but whether they are relevant to human behavior is unclear. Here, we identified parallel phenotypes in mice and humans resulting from a common single-nucleotide polymorphism in the brain-derived neurotrophic factor (BDNF) gene, which is involved in anxiety-related behavior. An inbred genetic knock-in mouse strain expressing the variant BDNF recapitulated the phenotypic effects of the human polymorphism. Both were impaired in extinguishing a conditioned fear response, which was paralleled by atypical frontoamygdala activity in humans. Thus, this variant BDNF allele may play a role in anxiety disorders showing impaired learning of cues that signal safety versus threat and in the efficacy of treatments that rely on extinction mechanisms, such as exposure therapy.
引用
收藏
页码:863 / 866
页数:4
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