人类疼痛体验中大脑皮层对上下文信息和感觉信息的时空整合。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-11-13 eCollection Date: 2024-11-01 DOI:10.1371/journal.pbio.3002910
Suhwan Gim, Seok-Jun Hong, Elizabeth A Reynolds Losin, Choong-Wan Woo
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引用次数: 0

摘要

疼痛并不仅仅是有害输入的反映。相反,它是通过将当前预测与传入的感觉输入进行动态整合而形成的。然而,支撑这种整合的行为和神经过程的时间动态仍然难以捉摸。在目前这项涉及 59 名人类参与者的研究中,我们发现了一系列大脑介导因素,这些介导因素将线索诱导的预期与有毒输入整合到使用半圆形量表设计的持续疼痛预测中,以捕捉评级轨迹。时间中介分析显示,在整合的早期到中期阶段,前顶叶和背侧注意网络区域(如外侧前额叶、运动前叶和顶叶皮层)中介了线索效应。相反,在整合的中后期阶段,躯体运动网络区介导了刺激强度的效应,这表明整合是沿着从联想到感觉运动的大脑皮层系统层次进行的。我们的研究结果加深了人们对大脑如何随着时间的推移将情境和感觉信息整合到疼痛体验中的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatiotemporal integration of contextual and sensory information within the cortical hierarchy in human pain experience.

Pain is not a mere reflection of noxious input. Rather, it is constructed through the dynamic integration of current predictions with incoming sensory input. However, the temporal dynamics of the behavioral and neural processes underpinning this integration remain elusive. In the current study involving 59 human participants, we identified a series of brain mediators that integrated cue-induced expectations with noxious inputs into ongoing pain predictions using a semicircular scale designed to capture rating trajectories. Temporal mediation analysis revealed that during the early-to-mid stages of integration, the frontoparietal and dorsal attention network regions, such as the lateral prefrontal, premotor, and parietal cortex, mediated the cue effects. Conversely, during the mid-to-late stages of integration, the somatomotor network regions mediated the effects of stimulus intensity, suggesting that the integration occurs along the cortical hierarchy from the association to sensorimotor brain systems. Our findings advance the understanding of how the brain integrates contextual and sensory information into pain experience over time.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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