ISSN 1671-3710
CN 11-4766/R
主办:中国科学院心理研究所
出版:科学出版社

心理科学进展 ›› 2026, Vol. 34 ›› Issue (9): 1646-1662.doi: 10.3724/SP.J.1042.2026.1646 cstr: 32111.14.2026.1646

• 研究前沿 • 上一篇    下一篇

安全学习与焦虑障碍: 三阶段神经机制框架

董展鹏, 张婕, 张亚蕊, 雷怡   

  1. 四川师范大学脑与心理科学研究院, 成都 610066
  • 收稿日期:2025-09-01 出版日期:2026-09-15 发布日期:2026-07-20
  • 基金资助:
    国家自然科学基金面上项目(32271142)、教育部哲学社会科学研究重大课题攻关项目(21JZD063)、四川省科技计划(2025NSFSC2019)资助

Safety learning and anxiety disorders: A three-stage neural mechanism framework

DONG Zhanpeng, ZHANG Jie, ZHANG Yarui, LEI Yi   

  1. Institute of Brain and Psychological Sciences, Sichuan Normal University, Chengdu 610066, China
  • Received:2025-09-01 Online:2026-09-15 Published:2026-07-20

摘要: 安全学习是指个体通过识别安全信号(预示无威胁的线索)来抑制恐惧的适应性机制, 其功能受损与焦虑及相关障碍的发生密切相关。基于现有研究, 本研究尝试提出一个由“安全的感知评估、安全的习得以及安全的行为表达”三阶段构成的安全学习神经机制框架, 强调焦虑障碍个体在安全学习三阶段表现出相应的神经机制异常:在感知评估阶段表现为以岛叶-感知皮层为核心的相关回路异常, 影响个体有效识别安全线索; 在习得阶段表现为中脑-纹状体回路的异常, 阻碍个体安全联结的建立与积极情绪体验的获取; 在行为表达阶段表现为以海马为核心的抑制回路功能异常, 使个体难以提取安全记忆以抑制恐惧反应。未来研究应通过更高生态效度的范式和测量手段, 揭示焦虑个体在安全学习中的阶段性异常, 以促进安全学习在临床干预中的转化应用。

关键词: 安全学习, 焦虑, 神经机制

Abstract: Safety learning refers to an adaptive psychological mechanism through which individuals identify safety signals that predict the absence of threat, thereby inhibiting fear responses and facilitating effective adaptation to complex environments. Impairments in this mechanism have been closely linked to a wide range of anxiety and related disorders. However, existing research has predominantly interpreted the pathogenesis of anxiety from the perspectives of fear learning or fear extinction, which has proven insufficient to fully account for core clinical features such as difficulties in safety discrimination, diminished positive emotional experience, and failures in fear inhibition. In light of these limitations, the present article systematically reviews evidence from animal models, human behavioral studies, and neuroimaging research, and proposes a three-stage neural framework of safety learning—comprising safety perception and evaluation, safety acquisition, and safety expression—to more comprehensively characterize the dynamic processes of safety learning and their abnormalities in anxiety disorders.
According to this framework, safety learning can be divided into three stages: (1) Safety perception and evaluation: At this stage, individuals detect external cues and rapidly evaluate their safety value. This process primarily relies on functional networks involving the thalamus, the sensory cortices, the insula, and the amygdala, which jointly support the early analysis of whether a stimulus signals safety. (2) Safety acquisition comprises two interrelated sub-processes: The first is the formation and maintenance of safety associations, whereby stable links between conditioned stimuli and non-threatening outcomes are established through prediction-error-driven learning. The second is the acquisition of positive affect, whereby repeated exposure to safe outcomes confers positive emotional value to safety cues. This stage is supported by midbrain-striatal dopaminergic circuits that facilitate both safety association learning and positive emotional experience, while the long-term consolidation of safety associations depends on coordinated interactions between the hippocampus and the prefrontal cortex, providing a foundation for the subsequent retrieval and utilization of safety memories.(3) Safety expression, which refers to the effective use of learned safety signals to inhibit fear responses. The neural mechanisms underlying this stage involve interactions among limbic regions (such as the hippocampus and amygdala), the prefrontal cortex, and temporal cortical areas. These regions jointly support the context-dependent retrieval of safety memories, thereby enabling the suppression of fear-related behavior.
Building on this framework, the article further delineates stage-specific neural deficits in individuals with anxiety and related disorders. During the perception and evaluation stage, these individuals exhibit exaggerated threat perception and insufficient top-down cognitive regulation. During the acquisition stage, they show reduced efficiency in prediction error coding and attenuated positive emotional experience associated with safety signals. During the expression stage, impairments are evident in the retrieval of safety memories and in the inhibition of fear responses. Each of these behavioral abnormalities is accompanied by corresponding dysfunctions in specific brain regions and neural circuits.
Finally, the article highlights several directions for future research and clinical application. First, future studies should strengthen the use of conditioned inhibition paradigms in investigations of safety learning in anxious populations. To enhance ecological validity and translational relevance, researchers are encouraged to incorporate naturalistic stimuli with semantic or social attributes and to combine multimodal neural measurements with multivariate analytical approaches to systematically examine neural representations of safety learning and recall in anxiety. Second, given the pervasive deficit in positive emotional experience during safety learning among anxious individuals, future interventions should place greater emphasis on enhancing the encoding of safety value and positive emotional experience. Third, at the level of clinical translation, the proposed framework underscores the dynamic, multi-stage nature of safety learning, suggesting that intervention strategies should be informed by underlying neural mechanisms and developmental stages, and implemented in a staged and targeted manner to achieve more precise and effective treatment outcomes.

Key words: safety learning, anxiety, neural mechanisms

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