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应激诱导的恐惧记忆潜在分子过程的变化:对创伤后应激障碍及相关动物模型的影响。

Stress-induced changes in the molecular processes underlying fear memories: implications for PTSD and relevant animal models.

作者信息

Andero Raül

机构信息

Institut de Neurociències, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Barcelona, Spain.

Departament de Psicobiologia i de Metodologia de les Ciències de la Salut, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Barcelona, Spain.

出版信息

Mol Psychiatry. 2025 May;30(5):2219-2227. doi: 10.1038/s41380-025-02910-8. Epub 2025 Jan 31.

DOI:10.1038/s41380-025-02910-8
PMID:39890919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12014489/
Abstract

Most of the fear literature on humans and animals tests healthy individuals. However, fear memories can differ between healthy individuals and those previously exposed to traumatic stress, such as a car accident, sexual abuse, military combat and personal assault. Traumatic stress can lead to post-traumatic stress disorder (PTSD) which presents alterations in fear memories, such as an impairment of fear extinction and extinction recall. PTSD-like animal models are exposed to a single highly stressful experience in the laboratory, such as stress immobilization or single-prolonged stress. Some days later, animals exposed to a PTSD-like model can be tested in fear procedures that help uncover molecular mechanisms of fear memories. In this review, there are discussed the molecular mechanisms in stress-induced fear memories of patients with PTSD and PTSD-like animal models. The focus is on the effects of estradiol and cortisol/corticosterone hormones and of different genes, such as FKBP prolyl isomerase 5 gene (FKBP5) - FK506 binding protein 51 (FKBP51), pituitary adenylate cyclase-activating peptide (PACAP) - pituitary adenylate cyclase-activating polypeptide type I receptor (PAC1R), endocannabinoid (eCB) system and the tropomyosin receptor kinase B (TrkB) - brain-derived neurotrophic factor (BDNF). The conclusion is that greater emphasis should be placed on investigating the molecular mechanisms of fear memories in PTSD, through direct testing of patients with PTSD or the use of relevant PTSD-like models.

摘要

大多数关于人类和动物的恐惧文献都以健康个体为研究对象。然而,健康个体与那些曾经历过创伤性应激(如车祸、性虐待、军事战斗和人身攻击)的个体之间的恐惧记忆可能存在差异。创伤性应激可导致创伤后应激障碍(PTSD),其会使恐惧记忆出现改变,如恐惧消退和消退回忆受损。类PTSD动物模型在实验室中会经历单次高度应激体验,如应激固定或单次长时间应激。几天后,可通过恐惧程序对经历类PTSD模型的动物进行测试,以帮助揭示恐惧记忆的分子机制。在本综述中,将讨论PTSD患者和类PTSD动物模型应激诱导恐惧记忆中的分子机制。重点关注雌二醇和皮质醇/皮质酮激素以及不同基因的作用,如FK506结合蛋白脯氨酰异构酶5基因(FKBP5)-FK506结合蛋白51(FKBP51)、垂体腺苷酸环化酶激活肽(PACAP)-垂体腺苷酸环化酶激活多肽I型受体(PAC1R)、内源性大麻素(eCB)系统以及原肌球蛋白受体激酶B(TrkB)-脑源性神经营养因子(BDNF)。结论是,应更加重视通过直接测试PTSD患者或使用相关类PTSD模型来研究PTSD中恐惧记忆的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea2b/12014489/c518730cf989/41380_2025_2910_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea2b/12014489/38d9c0b86744/41380_2025_2910_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea2b/12014489/c518730cf989/41380_2025_2910_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea2b/12014489/38d9c0b86744/41380_2025_2910_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea2b/12014489/c518730cf989/41380_2025_2910_Fig2_HTML.jpg

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Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder.
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