{"title":"Transcutaneous vagus nerve stimulation modulates fear memory extinction and neural responses in humans.","authors":"Xuejiao Zhang, Yujing Sun, Chenhao Zhao, Feng Yu, Jiaying Li, Zongya Zhao, Sizhi Ai","doi":"10.1093/cercor/bhaf224","DOIUrl":null,"url":null,"abstract":"<p><p>Previous research has shown that transcutaneous auricular vagus nerve stimulation (tVNS) promotes declarative fear extinction, but its neural mechanisms in this process are still unclear. This study aimed to explore tVNS's impacts on physiological (skin conductance response [SCR]) and neural (event-related potentials, ERP) fear-related responses. Forty healthy participants were randomly assigned to the tVNS or Sham group. During a fear-conditioned memory paradigm, electroencephalograph (EEG) and SCR were measured. We analyzed SCR amplitude, ERP components, EEG signal spectral analysis, and the correlation between SCR and EEG metrics. Results showed that compared with the Sham group, the tVNS group had a remarkable decrease in SCR amplitudes for conditioned stimuli (CS+) during retrieval and recall, suggesting reduced sympathetic arousal. ERP analysis revealed a notable decline in late positive potential (LPP) (400-800 ms) amplitudes for CS+ in the tVNS group during these phases, indicating weakened neural reactivity. A significant group-by-phase interaction showed that tVNS effectively suppressed immediate and sustained fear responses, maintaining lower fear-related physiological and neural activity levels. These findings suggest that tVNS modulates neural circuits involved in fear processing, clarifies the mechanisms underlying fear extinction, and highlights its therapeutic potential for fear-related disorders.</p>","PeriodicalId":9715,"journal":{"name":"Cerebral cortex","volume":"35 8","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cerebral cortex","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/cercor/bhaf224","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Previous research has shown that transcutaneous auricular vagus nerve stimulation (tVNS) promotes declarative fear extinction, but its neural mechanisms in this process are still unclear. This study aimed to explore tVNS's impacts on physiological (skin conductance response [SCR]) and neural (event-related potentials, ERP) fear-related responses. Forty healthy participants were randomly assigned to the tVNS or Sham group. During a fear-conditioned memory paradigm, electroencephalograph (EEG) and SCR were measured. We analyzed SCR amplitude, ERP components, EEG signal spectral analysis, and the correlation between SCR and EEG metrics. Results showed that compared with the Sham group, the tVNS group had a remarkable decrease in SCR amplitudes for conditioned stimuli (CS+) during retrieval and recall, suggesting reduced sympathetic arousal. ERP analysis revealed a notable decline in late positive potential (LPP) (400-800 ms) amplitudes for CS+ in the tVNS group during these phases, indicating weakened neural reactivity. A significant group-by-phase interaction showed that tVNS effectively suppressed immediate and sustained fear responses, maintaining lower fear-related physiological and neural activity levels. These findings suggest that tVNS modulates neural circuits involved in fear processing, clarifies the mechanisms underlying fear extinction, and highlights its therapeutic potential for fear-related disorders.
期刊介绍:
Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included.
The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.