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

被引:0
|
作者
Andero, Rauel [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Autonoma Barcelona, Inst Neurociencies, Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Psicobiol & Metodol Ciencies Salut, Barcelona, Spain
[3] Ctr Invest Biomed Red Salud Mental CIBERSAM, Madrid, Spain
[4] Inst Invest & Innovacio Parc Tauli I3PT, Unitat Neurociencia Traslac, Parc Tauli Hosp Univ, Sabadell, Spain
[5] ICREA, Barcelona, Spain
关键词
PITUITARY-ADRENAL AXIS; SEX-DIFFERENCES; ENDOCANNABINOID SYSTEM; ANTIDEPRESSANT DRUGS; EXTINCTION; DISORDER; BDNF; EXPRESSION; RESPONSES; HORMONES;
D O I
10.1038/s41380-025-02910-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2219 / 2227
页数:9
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