López-López Beatriz, Crespo Inmaculada
Departamento de Psicobiología, CES Cardenal Cisneros (Centro Adscrito a la Universidad Complutense de Madrid), E-28006 Madrid, España.
Rev Neurol. 2025 Jul 23;80(6):33478. doi: 10.31083/RN33478.
INTRODUCTION: Post-traumatic stress disorder (PTSD) develops in response to a traumatic experience, whether real or threatening, which produces emotions of intense fear and memory problems, significantly damaging the quality of life of those who manifest it. In recent years, anatomical-functional changes in the amygdala-hippocampus-prefrontal cortex circuit have begun to be studied as a key factor in the prevention, vulnerability, and treatment of PTSD, with neuroplasticity being one of the factors of greatest interest. Therefore, this review will address the latest published data regarding PTSD and neuroplasticity. DEVELOPMENT: Data from preclinical and clinical models support that a traumatic experience modifies both synaptic plasticity through electrophysiological and chemical variables, as well as myelin plasticity which enables short and long-distance connections. This remodelling of circuitry is crucial for the development of PTSD. However, it is also closely associated with prevention and positive treatment outcomes. Variables such as social support or the use of psychotherapy following a traumatic experience are linked to a good prognosis. CONCLUSIONS: Therefore, there is an interesting connection between neuroplasticity and PTSD, although many questions remain open today, along with promising lines of prevention and intervention, including psychedelic substances.
引言:创伤后应激障碍(PTSD)是因创伤性经历而产生的,无论这种经历是真实的还是具有威胁性的,都会引发强烈的恐惧情绪和记忆问题,严重损害患者的生活质量。近年来,杏仁核 - 海马体 - 前额叶皮质回路的解剖学 - 功能变化已开始被研究,被视为创伤后应激障碍预防、易感性和治疗的关键因素,其中神经可塑性是最受关注的因素之一。因此,本综述将探讨关于创伤后应激障碍和神经可塑性的最新发表数据。 进展:临床前和临床模型的数据表明,创伤性经历会通过电生理和化学变量改变突触可塑性,以及影响髓鞘可塑性,而髓鞘可塑性有助于实现短距离和长距离连接。这种神经回路的重塑对于创伤后应激障碍的发展至关重要。然而,它也与预防和积极的治疗结果密切相关。诸如社会支持或创伤经历后使用心理治疗等变量与良好的预后相关。 结论:因此,神经可塑性与创伤后应激障碍之间存在着有趣的联系,尽管如今仍有许多问题有待解决,但也有包括迷幻物质在内的有前景的预防和干预途径。
Rev Neurol. 2025-7-23
Psychopharmacol Bull. 2024-7-8
Cochrane Database Syst Rev. 2016-4-4
2025-1
Cochrane Database Syst Rev. 2013-12-13
Cochrane Database Syst Rev. 2016-10-11
Cochrane Database Syst Rev. 2021-12-6
Nat Neurosci. 2023-12
Trauma Violence Abuse. 2024-4
Neuropsychopharmacology. 2023-1