Department of Psychology, Uppsala University, Uppsala, Sweden.
Transl Psychiatry. 2012 Feb 7;2(2):e76. doi: 10.1038/tp.2012.5.
Fear memory persistence, central for the development and maintenance of anxiety disorders, is partially genetically controlled. Recently, consolidation and reconsolidation processes have been reported to affect fear memory stability and integrity. This study explored the impact of reconsolidation processes and genetic make-up on fear reacquisition by manipulating reconsolidation, using extinction performed outside or inside a reconsolidation interval. Reacquisition measured by skin conductance responses was stronger in individuals that extinguished outside (6 h) than inside (10 min) the reconsolidation interval. However, the effect was predominantly present in val/val homozygotes of the functional val158met polymorphism of the catechol O-methyltransferase (COMT) enzyme and in short-allele carriers of the serotonin-transporter length 5-HTTLPR polymorphism. These results demonstrate that reconsolidation of human fear memory is influenced by dopamine and serotonin-related genes.
恐惧记忆的持久性是焦虑障碍发生和维持的关键,部分受遗传控制。最近的研究表明,巩固和再巩固过程会影响恐惧记忆的稳定性和完整性。本研究通过在再巩固间隔内或外进行消退来操纵再巩固,以探索再巩固过程和遗传构成对恐惧再获得的影响。通过皮肤电反应测量的再获得在再巩固间隔外(6 小时)消退的个体中比在再巩固间隔内(10 分钟)消退的个体更强。然而,这种影响主要存在于儿茶酚氧位甲基转移酶(COMT)酶的功能性 val158met 多态性的 val/val 纯合子和 5-羟色胺转运体长度 5-HTTLPR 多态性的短等位基因携带者中。这些结果表明,人类恐惧记忆的再巩固受多巴胺和 5-羟色胺相关基因的影响。