Genetic Gating of Human Fear Learning and Extinction: Possible Implications for Gene-Environment Interaction in Anxiety Disorder

被引:189
作者
Lonsdorf, Tina B. [1 ,2 ]
Weike, Almut I. [3 ]
Nikamo, Pernilla [4 ]
Schalling, Martin [4 ]
Hamm, Alfons O. [3 ,5 ]
Ohman, Arne [1 ,2 ,5 ]
机构
[1] Karolinska Inst, Psychol Sect, Dept Clin Neurosci, SE-17177 Stockholm, Sweden
[2] Stockholm Brain Inst, Stockholm, Sweden
[3] Ernst Moritz Arndt Univ Greifswald, Dept Clin & Biol Psychol, D-17487 Greifswald, Germany
[4] Karolinska Inst, Dept Mol Med & Surg, Neurogenet Unit, SE-17177 Stockholm, Sweden
[5] Univ Florida, Ctr Study Emot & Attent, Gainesville, FL 32611 USA
基金
瑞典研究理事会;
关键词
SEROTONIN TRANSPORTER; THEORY PERSPECTIVE; SKIN-CONDUCTANCE; AMYGDALA; POLYMORPHISM; METAANALYSIS; AWARENESS; EMOTION; DISSOCIATION; PREPAREDNESS;
D O I
10.1111/j.1467-9280.2009.02280.x
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Pavlovian fear conditioning is a widely used model of the acquisition and extinction of fear. Neural findings suggest that the amygdala is the core structure for fear acquisition, whereas prefrontal cortical areas are given pivotal roles in fear extinction. Forty-eight volunteers participated in a fear-conditioning experiment, which used fear potentiation of the startle reflex as the primary measure to investigate the effect of two genetic polymorphisms (5-HTTLPR and COMTval158met) on conditioning and extinction of fear. The 5-HTTLPR polymorphism, located in the serotonin transporter gene, is associated with amygdala reactivity and neuroticism, whereas the COMTval158met polymorphism, which is located in the gene coding for catechol-O-methyltransferase (COMT), a dopamine-degrading enzyme, affects prefrontal executive functions. Our results show that only carriers of the 5-HTTLPR s allele exhibited conditioned startle potentiation, whereas carriers of the COMT met/met genotype failed to extinguish conditioned fear. These results may have interesting implications for understanding gene-environment interactions in the development and treatment of anxiety disorders.
引用
收藏
页码:198 / 206
页数:9
相关论文
共 38 条
[1]   The promise of extinction research for the prevention and treatment of anxiety disorders [J].
Anderson, Kathleen C. ;
Insel, Thomas R. .
BIOLOGICAL PSYCHIATRY, 2006, 60 (04) :319-321
[2]  
Barlow D.H., 2014, Clinical handbook of psychological disorders: A step-by-step treatment manual, V5th
[3]   DOUBLE DISSOCIATION OF CONDITIONING AND DECLARATIVE KNOWLEDGE RELATIVE TO THE AMYGDALA AND HIPPOCAMPUS IN HUMANS [J].
BECHARA, A ;
TRANEL, D ;
DAMASIO, H ;
ADOLPHS, R ;
ROCKLAND, C ;
DAMASIO, AR .
SCIENCE, 1995, 269 (5227) :1115-1118
[4]   The catechol-O-methyltransferase polymorphism:: Relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes [J].
Bilder, RM ;
Volavka, J ;
Lachman, HM ;
Grace, AA .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (11) :1943-1961
[5]   A modern learning theory perspective on the etiology of panic disorder [J].
Bouton, ME ;
Mineka, S ;
Barlow, DH .
PSYCHOLOGICAL REVIEW, 2001, 108 (01) :4-32
[6]   Long story short: the serotonin transporter in emotion regulation and social cognition [J].
Canli, Turhan ;
Lesch, Klaus-Peter .
NATURE NEUROSCIENCE, 2007, 10 (09) :1103-1109
[7]   TEMPERAMENT, PERSONALITY, AND THE MOOD AND ANXIETY DISORDERS [J].
CLARK, LA ;
WATSON, D ;
MINEKA, S .
JOURNAL OF ABNORMAL PSYCHOLOGY, 1994, 103 (01) :103-116
[8]   The amygdala: vigilance and emotion [J].
Davis, M ;
Whalen, PJ .
MOLECULAR PSYCHIATRY, 2001, 6 (01) :13-34
[9]   The neuroscience of mammalian associative learning [J].
Fanselow, MS ;
Poulos, AM .
ANNUAL REVIEW OF PSYCHOLOGY, 2005, 56 :207-234
[10]   Human fear conditioning is related to dopaminergic and serotonergic biological markers [J].
Garpenstrand, H ;
Annas, P ;
Ekblom, J ;
Oreland, L ;
Fredrikson, M .
BEHAVIORAL NEUROSCIENCE, 2001, 115 (02) :358-364