功能性MRI揭示人类颈脊髓和脑干疼痛处理的情绪调节

A McIverTheresa, K. Jennifer, W StromanPatrick
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引用次数: 3

摘要

背景:先前的研究表明情绪状态可以影响疼痛感知。当有害刺激与负面情绪刺激相结合时,对有害刺激的感知会因负面情绪刺激的厌恶联想而增强。相反,疼痛评分随着积极情绪的影响而降低。本研究的目的是利用功能性MRI表征脊髓和脑干疼痛处理的情绪调节。方法:21名健康的右撇子女性,年龄18-30岁(M年龄= 21.5岁),在完成热痛评分任务的同时对脊髓和脑干进行了功能磁共振成像扫描。参与者在观看不同情绪情境(积极、中性或消极)的图像时,对右手大鱼际上方进行了有害的热刺激,并提供了疼痛强度和不愉快程度的评级。结果:疼痛评分对情绪情境有显著影响,消极情绪情境引起的疼痛强度(M = 48.74, SD = 10.60)和不愉快(M = 36.60, SD = 11.92)评分显著高于积极情绪情境(M = 44.22, SD = 10.75)和不愉快(M = 29.05, SD = 10.09)评分(p < 0.01)。除了复制疼痛感知的情绪调节效应外,脊髓和脑干区域的BOLD反应已知在疼痛处理中起作用,也显示出对疼痛处理的下行情绪调节的影响。这些区域包括同侧T1脊髓节段的背角(与受刺激皮肤节对应的节段的尾侧),以及脑干中靠近尾侧髓质的背网状核和脑桥的臂旁核的区域(p < 0.001)。结论:这些发现对疼痛加工的下行情绪调节的神经关联提供了新的见解。此外,本研究强调了未来研究的重点领域,以检查脊髓和脑干中疼痛神经处理的情绪调节的潜在个体水平差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional MRI Reveals Emotional Modulation of Pain Processing in the Human Cervical Spinal Cord and Brainstem
Background: Prior research has demonstrated that emotional state can influence pain perception. If a noxious stimulus is coupled with a negative emotional stimulus, the perception of the noxious stimulus will be heightened by the aversive associations of the negative emotional stimulus. In contrast, pain ratings decrease with positive emotional influence. The aim of the current study was to characterize the emotional modulation of pain processing in the spinal cord and brainstem using functional MRI. Methods: Twenty-one healthy, right-handed females, aged 18-30 (M age = 21.5) underwent an fMRI scan of the spinal cord and brainstem while completing a heat pain-rating task. Participants received noxious thermal stimulus to the thenar eminence of the right hand while viewing images of varying emotional contexts (Positive, Neutral, or Negative), and provided ratings of pain Intensity and Unpleasantness. Results: Pain ratings reflected a significant effect for emotional context, with the Negative emotional condition eliciting significantly greater pain Intensity (M = 48.74, SD = 10.60) and Unpleasantness (M = 36.60, SD = 11.92) ratings than the Positive Intensity (M = 44.22, SD = 10.75) and Unpleasantness (M = 29.05, SD = 10.09) ratings (p < 0.01). In addition to replicating the well-established effect for emotional modulation of pain perception, BOLD responses in regions of the spinal cord and brainstem that are known to function in pain processing also exhibited an effect for descending emotional modulation of pain processing. These regions included the ipsilateral, dorsal horn of the T1 spinal cord segment (caudal to the segment corresponding to the stimulated dermatome), as well as regions in the brainstem approximating the dorsal reticular nucleus of the caudal medulla and the parabrachial nuclei of the pons (p < 0.001). Conclusion: These findings provide novel insight into the neural correlates of descending emotional modulation of pain processing. Furthermore, this study highlights key areas of focus for future research to examine potential individual-level differences in emotional modulation of pain neural processing in the spinal cord and brainstem.
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