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疼痛通路与神经系统可塑性:疼痛中的学习与记忆

Pain Pathways and Nervous System Plasticity: Learning and Memory in Pain.

作者信息

McCarberg Bill, Peppin John

机构信息

Chronic Pain Management Program, Kaiser Permanente, San Diego, California; †University of California, San Diego, California; ‡Neighborhood Health, San Diego, California; §College of Osteopathic Medicine, Marian University, Indianapolis, Indiana; ¶John F. Peppin, DO, LLC, Hamden, Connecticut.

出版信息

Pain Med. 2019 Dec 1;20(12):2421-2437. doi: 10.1093/pm/pnz017.

Abstract

Objective This article reviews the structural and functional changes in pain chronification and explores the association between memory and the development of chronic pain. Methods PubMed was searched using the terms "chronic pain," "central sensitization," "learning," "memory," "long-term potentiation," "long-term depression," and "pain memory." Relevant findings were synthesized into a narrative of the processes affecting pain chronification. Results Pain pathways represent a complex sensory system with cognitive, emotional, and behavioral influences. Anatomically, the hippocampus, amygdala, and anterior cortex-central to the encoding and consolidation of memory-are also implicated in experiential aspects of pain. Common neurotransmitters and similar mechanisms of neural plasticity (eg, central sensitization, long-term potentiation) suggest a mechanistic overlap between chronic pain and memory. These anatomic and mechanistic correlates indicate that chronic pain and memory intimately interact on several levels. Longitudinal imaging studies suggest that spatiotemporal reorganization of brain activity accompanies the transition to chronic pain, during which the representation of pain gradually shifts from sensory to emotional and limbic structures. Conclusions The chronification of pain can be conceptualized as activity-induced plasticity of the limbic-cortical circuitry resulting in reorganization of the neocortex. The state of the limbic-cortical network determines whether nociceptive signals are transient or chronic by extinguishing pathways or amplifying signals that intensify the emotional component of nociceptive inputs. Thus, chronic pain can be seen as the persistence of the memory of pain and/or the inability to extinguish painful memories. Ideally, pharmacologic, physical, and/or psychological approaches should reverse the reorganization accompanying chronic pain.

摘要

目的 本文回顾疼痛慢性化过程中的结构和功能变化,并探讨记忆与慢性疼痛发展之间的关联。方法 使用 “慢性疼痛”“中枢敏化”“学习”“记忆”“长时程增强”“长时程抑制” 和 “疼痛记忆” 等术语在PubMed数据库进行检索。将相关研究结果综合成一个关于影响疼痛慢性化过程的叙述。结果 疼痛通路是一个具有认知、情感和行为影响的复杂感觉系统。在解剖学上,对记忆编码和巩固至关重要的海马体、杏仁核和前额叶皮质也与疼痛的体验方面有关。常见的神经递质和相似的神经可塑性机制(如中枢敏化、长时程增强)表明慢性疼痛与记忆之间存在机制上的重叠。这些解剖学和机制上的关联表明慢性疼痛和记忆在多个层面上密切相互作用。纵向影像学研究表明,大脑活动的时空重组伴随着向慢性疼痛的转变,在此过程中,疼痛的表征逐渐从感觉结构转移到情感和边缘系统结构。结论 疼痛的慢性化可被概念化为边缘 - 皮质神经回路的活动诱导可塑性,导致新皮质的重组。边缘 - 皮质网络的状态通过消除通路或放大增强伤害性输入情感成分的信号来决定伤害性信号是短暂的还是慢性的。因此,慢性疼痛可被视为疼痛记忆的持续存在和 / 或无法消除痛苦记忆。理想情况下,药物、物理和 / 或心理方法应逆转伴随慢性疼痛的重组。

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