Guo Yifei, Wang Yuzheng, Sun Yabin, Wang Jin-Yan
Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of SciencesBeijing, China; School of Humanities, University of Chinese Academy of SciencesBeijing, China.
Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences Beijing, China.
Front Comput Neurosci. 2016 Apr 28;10:41. doi: 10.3389/fncom.2016.00041. eCollection 2016.
The transition from acute pain to chronic pain entails considerable changes of patients at multiple levels of the nervous system and in psychological states. An accurate differentiation between acute and chronic pain is essential in pain management as it may help optimize analgesic treatments according to the pain state of patients. Given that acute and chronic pain could modulate brain states in different ways and that brain states could greatly shape the neural processing of external inputs, we hypothesized that acute and chronic pain would show differential effects on cortical responses to non-nociceptive sensory information. Here by analyzing auditory-evoked potentials (AEPs) to pure tones in rats with acute or chronic pain, we found opposite influences of acute and chronic pain on cortical responses to auditory inputs. In particular, compared to no-pain controls, the N100 wave of rat AEPs was significantly enhanced in rats with acute pain but significantly reduced in rats with chronic pain, indicating that acute pain facilitated cortical processing of auditory information while chronic pain exerted an inhibitory effect. These findings could be justified by the fact that individuals suffering from acute or chronic pain would have different vigilance states, i.e., the vigilance level to external sensory stimuli would be increased with acute pain, but decreased with chronic pain. Therefore, this auditory response holds promise of being a brain signature to differentiate acute and chronic pain. Instead of investigating the pain system per se, the study of pain-induced influences on cortical processing of non-nocicpetive sensory information might represent a potential strategy to monitor the progress of pain chronification in clinical applications.
从急性疼痛到慢性疼痛的转变在神经系统的多个层面以及心理状态方面给患者带来了相当大的变化。在疼痛管理中,准确区分急性疼痛和慢性疼痛至关重要,因为这有助于根据患者的疼痛状态优化镇痛治疗。鉴于急性疼痛和慢性疼痛可能以不同方式调节脑状态,且脑状态会极大地塑造外部输入的神经处理过程,我们推测急性疼痛和慢性疼痛对皮质对非伤害性感觉信息的反应会产生不同影响。在此,通过分析急性或慢性疼痛大鼠对纯音的听觉诱发电位(AEP),我们发现急性疼痛和慢性疼痛对皮质对听觉输入的反应有相反影响。特别是,与无疼痛对照组相比,急性疼痛大鼠的AEP的N100波显著增强,而慢性疼痛大鼠的N100波显著降低,这表明急性疼痛促进了听觉信息的皮质处理,而慢性疼痛则产生了抑制作用。这些发现可以通过以下事实来解释,即患有急性或慢性疼痛的个体具有不同的警觉状态,也就是说,对外部感觉刺激的警觉水平在急性疼痛时会升高,而在慢性疼痛时会降低。因此,这种听觉反应有望成为区分急性疼痛和慢性疼痛的脑特征。对疼痛引起的对非伤害性感觉信息的皮质处理的影响进行研究,而不是本身研究疼痛系统,可能代表了一种在临床应用中监测疼痛慢性化进展的潜在策略。