Zimmermann Kelsey S, Richardson Rick, Baker Kathryn D
School of Psychology, University of New South Wales (UNSW), Sydney, NSW 2052, Australia.
Brain Sci. 2019 Mar 18;9(3):65. doi: 10.3390/brainsci9030065.
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.
青少年期出现的焦虑症是一项重大负担,且治疗起来极具挑战性,这在很大程度上是由于该年龄组在暴露疗法后复发率很高。这种持续恐惧的模式在所有物种中都存在;相对于年幼和年长的个体,青少年一贯表现出较差的消退能力,而消退是暴露疗法的一个关键过程。这表明,恐惧消退背后的神经过程在青少年期会暂时但严重受损。恐惧及消退相关记忆的形成、提取和修改由一个前脑网络调节,该网络由前额叶皮质(PFC)、杏仁核和海马体组成。这些区域在生命早期会经历显著的成熟变化,在整个青少年期会出现结构和功能的独特改变。在这篇综述中,我们主要关注其中两个区域——PFC和杏仁核——并讨论可塑性、突触传递、抑制/兴奋及连接性(包括海马体传入纤维对PFC的调节)的变化如何可能导致消退记忆保持的短暂缺陷。我们最后简要考虑了在这个青少年脆弱期暴露于压力如何会永久性地破坏神经发育,导致情绪调节通路的持久损伤。