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本文引用的文献

1
Opposite effects of fear conditioning and extinction on dendritic spine remodelling.恐惧条件反射和消退对树突棘重塑的相反作用。
Nature. 2012 Feb 19;483(7387):87-91. doi: 10.1038/nature10792.
2
Fear extinction as a model for translational neuroscience: ten years of progress.恐惧消除作为转化神经科学的模型:十年的进展。
Annu Rev Psychol. 2012;63:129-51. doi: 10.1146/annurev.psych.121208.131631.
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Development of the GABAergic system from birth to adolescence.从出生到青春期 GABA 能系统的发育。
Neuroscientist. 2012 Dec;18(6):613-30. doi: 10.1177/1073858411422114. Epub 2011 Sep 27.
4
Selective early-acquired fear memories undergo temporary suppression during adolescence.选择性早期获得的恐惧记忆在青春期会经历暂时的抑制。
Proc Natl Acad Sci U S A. 2011 Jan 18;108(3):1182-7. doi: 10.1073/pnas.1012975108. Epub 2011 Jan 10.
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Service utilization for lifetime mental disorders in U.S. adolescents: results of the National Comorbidity Survey-Adolescent Supplement (NCS-A).美国青少年终身精神障碍的服务利用情况:国家共病调查-青少年增补调查(NCS-A)的结果。
J Am Acad Child Adolesc Psychiatry. 2011 Jan;50(1):32-45. doi: 10.1016/j.jaac.2010.10.006. Epub 2010 Dec 3.
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Lifetime prevalence of mental disorders in U.S. adolescents: results from the National Comorbidity Survey Replication--Adolescent Supplement (NCS-A).美国青少年精神障碍终身患病率:全国共病调查再现-青少年增补研究(NCS-A)的结果。
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7
Impaired extinction retention in adolescent rats: effects of D-cycloserine.青少年大鼠的消退保持能力受损:D-环丝氨酸的影响。
Neuropsychopharmacology. 2010 Sep;35(10):2134-42. doi: 10.1038/npp.2010.92. Epub 2010 Jun 30.
8
Immunohistochemical analyses of long-term extinction of conditioned fear in adolescent rats.青少年期条件性恐惧消退的免疫组化分析。
Cereb Cortex. 2011 Mar;21(3):530-8. doi: 10.1093/cercor/bhq116. Epub 2010 Jun 24.
9
Extinction in preweanling rats does not involve NMDA receptors.新生期大鼠的灭绝不涉及 NMDA 受体。
Neurobiol Learn Mem. 2010 Sep;94(2):176-82. doi: 10.1016/j.nlm.2010.05.004. Epub 2010 May 21.
10
A critical role for alpha4betadelta GABAA receptors in shaping learning deficits at puberty in mice.alpha4betadelta GABAA 受体在塑造青春期小鼠学习缺陷方面的关键作用。
Science. 2010 Mar 19;327(5972):1515-8. doi: 10.1126/science.1184245.

在老鼠和人类的发育过程中,恐惧学习发生改变。

Altered fear learning across development in both mouse and human.

机构信息

Department of Psychiatry, Weill Cornell Medical College of Cornell University, New York, NY 10065, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Oct 2;109(40):16318-23. doi: 10.1073/pnas.1206834109. Epub 2012 Sep 17.

DOI:10.1073/pnas.1206834109
PMID:22988092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3479553/
Abstract

The only evidence-based behavioral treatment for anxiety and stress-related disorders involves desensitization techniques that rely on principles of extinction learning. However, 40% of patients do not respond to this treatment. Efforts have focused on individual differences in treatment response, but have not examined when, during development, such treatments may be most effective. We examined fear-extinction learning across development in mice and humans. Parallel behavioral studies revealed attenuated extinction learning during adolescence. Probing neural circuitry in mice revealed altered synaptic plasticity of prefrontal cortical regions implicated in suppression of fear responses across development. The results suggest a lack of synaptic plasticity in the prefrontal regions, during adolescence, is associated with blunted regulation of fear extinction. These findings provide insight into optimizing treatment outcomes for when, during development, exposure therapies may be most effective.

摘要

唯一基于证据的焦虑和压力相关障碍的行为治疗涉及脱敏技术,该技术依赖于消除学习的原则。然而,40%的患者对此治疗没有反应。人们一直致力于研究治疗反应的个体差异,但尚未研究在何时,在发展过程中,这些治疗可能最有效。我们在小鼠和人类中研究了恐惧消除学习的发展情况。平行的行为研究表明,青少年时期的消退学习减弱。对小鼠神经回路的探测揭示了前额皮质区域的突触可塑性发生改变,这些区域在整个发育过程中对抑制恐惧反应具有重要作用。结果表明,青春期前额叶区域缺乏突触可塑性与恐惧消退的调节能力减弱有关。这些发现为优化治疗结果提供了线索,即何时、在发展过程中,暴露疗法可能最有效。