膜受体对共情疼痛调节的影响

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Guilherme Pegas Teixeira , Leandro Rocha , Robson Xavier Faria
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引用次数: 0

摘要

人类可以估计彼此的痛苦,并提供适当的护理来减轻痛苦。移情技能对参与疼痛管理的护理人员至关重要;因此,教育项目和理论都强调了共情在减轻疼痛强度方面的积极作用。人们还普遍认为,如果护理人员缺乏同理心,他们会低估患者的疼痛强度,而这种缺乏同理心的态度会对疼痛强度的感知产生负面影响。功能性磁共振成像和其他方法显示,对疼痛的同理心被认为激活了疼痛基质的情感动机成分,包括脑岛前部、扣带皮层中部和前部以及杏仁核。这个核心神经网络的活动反映了激活我们对疼痛反应的情感体验,并为我们理解自己和他人的情绪奠定了神经基础。此外,多种因素可以调节对疼痛的共情强度,如催产素和抗利尿激素受体。因此,我们有选择性地回顾了膜受体调节这种疼痛模式的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The impact of membrane receptors on modulating empathic pain

The impact of membrane receptors on modulating empathic pain
Humans can estimate each other's pain and provide adapted care to reduce it. Empathetic skills are crucial for caregivers involved in pain management; consequently, educational programs and theories have emphasized the positive role of empathy in reducing pain intensity. It is also widely assumed that if caregivers lack empathy, they will underestimate pain intensity in their patients, and this unempathetic attitude can negatively influence pain intensity perception. Empathy for pain is thought to activate the affective‒motivational components of the pain matrix, which includes the anterior insula, middle and anterior cingulate cortices and amygdala, as indicated by functional magnetic resonance imaging and other methodologies. Activity in this core neural network reflects the affective experience that activates our responses to pain and lays the neural foundation for our understanding of our own emotions and those of others. Additionally, a variety of factors can regulate the intensity of empathy for pain, such as oxytocin and vasopressin receptors. Therefore, we selectively review the molecular mechanisms by which membrane receptors modulate this pain modality.
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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