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Maturational Changes in Prefrontal and Amygdala Circuits in Adolescence: Implications for Understanding Fear Inhibition during a Vulnerable Period of Development

机译:青春期前额叶和杏仁核回路的成熟变化:在脆弱的发育时期理解恐惧抑制的含义

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摘要

Anxiety disorders that develop in adolescence represent a significant burden and are particularly challenging to treat, due in no small part to the high occurrence of relapse in this age group following exposure therapy. This pattern of persistent fear is preserved across species; relative to those younger and older, adolescents consistently show poorer extinction, a key process underpinning exposure therapy. This suggests that the neural processes underlying fear extinction are temporarily but profoundly compromised during adolescence. The formation, retrieval, and modification of fear- and extinction-associated memories are regulated by a forebrain network consisting of the prefrontal cortex (PFC), the amygdala, and the hippocampus. These regions undergo robust maturational changes in early life, with unique alterations in structure and function occurring throughout adolescence. In this review, we focus primarily on two of these regions—the PFC and the amygdala—and discuss how changes in plasticity, synaptic transmission, inhibition/excitation, and connectivity (including modulation by hippocampal afferents to the PFC) may contribute to transient deficits in extinction retention. We end with a brief consideration of how exposure to stress during this adolescent window of vulnerability can permanently disrupt neurodevelopment, leading to lasting impairments in pathways of emotional regulation.
机译:在青春期发展的焦虑症代表了沉重的负担,并且在治疗上尤其具有挑战性,这在很大程度上是由于该年龄段的暴露疗法后复发率很高。这种持续恐惧的模式在物种间得以保留。相对于年轻人和老年人,青少年的灭绝状况一直较差,这是暴露疗法的关键过程。这表明,恐惧消退的潜在神经过程在青春期被暂时性但深远地损害了。恐惧和与灭绝相关的记忆的形成,恢复和改变受前额神经网络调节,该网络由前额叶皮层(PFC),杏仁核和海马体组成。这些区域在生命早期经历了强大的成熟变化,整个青春期都发生了结构和功能的独特变化。在这篇综述中,我们主要关注这两个区域-PFC和杏仁核-并讨论可塑性,突触传递,抑制/激发和连接性(包括海马传入PFC的调节)的变化如何可能导致短暂性功能障碍在消光保持。最后,我们简要考虑一下在这个脆弱的青春期窗口中暴露于压力下如何永久性破坏神经发育,从而导致情绪调节途径的持久性损伤。

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