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Enhancing exposure-based therapy from a translational research perspective

期刊

BEHAVIOUR RESEARCH AND THERAPY
卷 45, 期 9, 页码 1987-2001

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.brat.2007.06.006

关键词

exposure therapy; extinction learning; anxiety disorders; phobias; D-cycloserine; NMDA; glycine; glutamate; translational research

资金

  1. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH078308] Funding Source: NIH RePORTER
  2. NIMH NIH HHS [R01 MH078308-01A1, R01 MH078308] Funding Source: Medline

向作者/读者索取更多资源

Combining an effective psychological treatment with conventional anxiolytic medication is typically not more effective than unimodal therapy for treating anxiety disorders. However, recent advances in the neuroscience of fear reduction have led to novel approaches for combining psychological therapy and pharmacological agents. Exposure-based treatments in humans partly rely on extinction to reduce the fear response in anxiety disorders. Animal studies have shown that D-cycloserine (DCS). a partial agonist at the glycine recognition site of the glutamatergic N-methyl-D-aspartate receptor facilitates extinction learning. Similarly, recent human trials have shown that DCS enhances fear reduction during exposure therapy of some anxiety disorders. This article discusses the biological and psychological mechanisms of extinction learning and the therapeutic value of DCS as an augmentation strategy for exposure therapy. Areas of future research will be identified. (c) 2007 Elsevier Ltd. All rights reserved.

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