Department of Life Science, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd, Taipei, 10617, Taiwan.
Interdisciplinary MRI/MRS Lab, Department of Electrical Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd, Taipei, 10617, Taiwan.
Mol Brain. 2018 Oct 1;11(1):55. doi: 10.1186/s13041-018-0398-z.
Neuropathic pain is a major worldwide health problem. Although central sensitization has been reported in well-established neuropathic conditions, information on the acute brain activation patterns in response to peripheral nerve injury is lacking. This study first mapped the brain activity in rats immediately following spared nerve injury (SNI) of the sciatic nerve. Using blood-oxygenation-level-dependent functional magnetic resonance imaging (BOLD-fMRI), we observed sustained activation in the bilateral insular cortices (ICs), primary somatosensory cortex (S1), and cingulate cortex. Second, this study sought to link this sustained activation pattern with brain sensitization. Using manganese-enhanced magnetic resonance imaging (MEMRI), we observed enhanced activity in the ipsilateral anterior IC (AIC) in free-moving SNI rats on Days 1 and 8 post-SNI. Furthermore, enhanced functional connectivity between the ipsilateral AIC, bilateral rostral AIC, and S1 was observed on Day 8 post-SNI. Chronic electrophysiological recording experiments were conducted to confirm the tonic neuronal activation in selected brain regions. Our data provide evidence of tonic activation-dependent brain sensitization during neuropathic pain development and offer evidence that the plasticity changes in the IC and S1 may contribute to neuropathic pain development.
神经病理性疼痛是一个全球性的重大健康问题。尽管在既定的神经病理性疾病中已经报道了中枢敏化,但关于外周神经损伤后大脑激活模式的信息仍然缺乏。本研究首先绘制了坐骨神经 spared nerve injury (SNI) 后大鼠的大脑活动图谱。使用血氧水平依赖功能磁共振成像 (BOLD-fMRI),我们观察到双侧岛叶皮层(IC)、初级体感皮层(S1)和扣带回皮层的持续激活。其次,本研究试图将这种持续的激活模式与大脑敏化联系起来。使用锰增强磁共振成像(MEMRI),我们观察到在 SNI 后第 1 天和第 8 天自由活动的 SNI 大鼠中,同侧前岛叶(AIC)的活性增强。此外,在 SNI 后第 8 天观察到同侧 AIC、双侧前 AIC 和 S1 之间的功能连接增强。进行慢性电生理记录实验以确认选定脑区的紧张性神经元激活。我们的数据提供了神经病理性疼痛发展过程中紧张性激活依赖性大脑敏化的证据,并提供了证据表明 IC 和 S1 中的可塑性变化可能有助于神经病理性疼痛的发展。