生理和社会疼痛共情的神经机制:fMRI研究的激活似然估计meta分析。

IF 2.9 2区 医学 Q2 NEUROSCIENCES
Peng Zhang, Lin Ding, Mingliang Wang, Shuyi Qiu
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引用次数: 0

摘要

本研究采用系统的元分析来阐明身体和社会痛苦共情的神经表征差异。为了解决这两种共情类型之间的神经功能相似性和差异这一关键问题,我们进行了一项基于激活似然估计坐标的meta分析,定量地综合了35项功能性MRI研究。主要发现如下:(1)身体疼痛共情表现出显著的左偏侧激活模式,涉及镜像神经元系统的核心区域,包括情绪共振(前扣带皮层、前额叶皮层)、情感认知整合(前脑岛)和动作理解(额下回、顶叶下叶);(ii)社会疼痛共情选择性激活心智化网络(背内侧前额叶皮层/内侧前额叶皮层);(iii)差异分析发现顶叶下小叶、前扣带皮层和额上回是核心区分区域,没有发现共享的激活脑区。这些发现提供了支持共情亚型之间神经基质功能分离的大规模证据,为共情的多维模型提供了重要的神经影像学证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neural mechanisms of physical and social pain empathy: an activation likelihood estimation meta-analysis of fMRI studies.

This study employed a systematic meta-analysis to elucidate neural representation differences between empathy for physical and social pain. Addressing the critical unresolved question of neurofunctional similarities and distinctions between these two empathy types, we performed an activation likelihood estimation coordinate-based meta-analysis, quantitatively synthesizing 35 functional MRI studies. Key findings revealed the following: (i) Physical pain empathy demonstrated significant left-lateralized activation patterns involving core regions of the mirror neuron system-including emotional resonance (anterior cingulate cortex, prefrontal cortex), affective-cognitive integration (anterior insula), and action comprehension (inferior frontal gyrus, inferior parietal lobule); (ii) social pain empathy selectively activated the mentalizing network (dorsomedial prefrontal cortex/medial prefrontal cortex); (iii) differential analyses identified the inferior parietal lobule, anterior cingulate cortex, and superior frontal gyrus as core discriminative regions, with no shared activated brain areas detected. These findings provide large-scale evidence supporting functional segregation in neural substrates between empathy subtypes, offering critical neuroimaging evidence for multidimensional models of empathy.

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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
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.
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