4.8 Article

Fear-Conditioning Mechanisms Associated with Trait Vulnerability to Anxiety in Humans

期刊

NEURON
卷 69, 期 3, 页码 563-571

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2010.12.034

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资金

  1. Medical Research Council [G120/919, U1055.02.002.00001.01]
  2. NIMH [RO1MH091848]
  3. Marie Curie Intra European Fellowship
  4. James S McDonnell Foundation
  5. University of Cambridge Behavioural and Clinical Neuroscience Institute
  6. Medical Research Council
  7. Wellcome Trust
  8. GlaxoSmithKline
  9. Lundbeck
  10. Lilly
  11. Medical Research Council [G0001354, G120/919, G1000183, G0001354B] Funding Source: researchfish
  12. MRC [G1000183, G120/919] Funding Source: UKRI

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Investigations of fear conditioning in rodents and humans have illuminated the neural mechanisms underlying cued and contextual fear. A critical question is how personality dimensions such as trait anxiety act through these mechanisms to confer vulnerability to anxiety disorders, and whether humans' ability to overcome acquired fears depends on regulatory skills not characterized in animal models. In a neuroimaging study of fear conditioning in humans, we found evidence for two independent dimensions of neurocognitive function associated with trait vulnerability to anxiety. The first entailed increased amygdala responsivity to phasic fear cues. The second involved impoverished ventral prefrontal cortical (vPFC) recruitment to downregulate both cued and contextual fear prior to omission (extinction) of the aversive unconditioned stimulus. These two dimensions may contribute to symptomatology differences across anxiety disorders; the amygdala mechanism affecting the development of phobic fear and the frontal mechanism influencing the maintenance of both specific fears and generalized anxiety.

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