Gu Xiaoping, Yang Liling, Wang Shuxing, Sung Backil, Lim Grewo, Mao Ji, Zeng Qing, Yang Chang, Mao Jianren
Department of Anesthesiology, Drum Tower Hospital, Nanjing, People's Republic of China.
Anesthesiology. 2008 Jan;108(1):113-21. doi: 10.1097/01.anes.0000296073.16972.13.
Radicular pain is a common and debilitating clinical pain condition. To date, the mechanisms of radicular pain remain unclear, partly because of the lack of suitable preclinical models. The authors report a modified rat model of radicular pain that could mimic a subset of clinical radicular pain conditions induced by the soft tissue compression on dorsal root ganglion.
A rat model of radicular pain was produced by infiltrating the L5 intervertebral foramen with 60 microl of a hemostatic matrix (SURGIFLO; Johnson & Johnson, Somerville, NJ) resulting in chronic compression of lumbar dorsal root ganglion. Thermal hyperalgesia and mechanical allodynia were measured with or without epidural treatment with triamcinolone. Western blot was used to assess the expression of the NR1 subunit of the N-methyl-D-aspartate receptor and inhibitory factor kappabeta-alpha, an inflammatory marker, within the affected L5 dorsal root ganglion and spinal cord dorsal horn.
Chronic compression of lumbar dorsal root ganglion resulted in: (1) persistent mechanical allodynia and thermal hyperalgesia up to 4 or 5 postoperative weeks and (2) up-regulation of the N-methyl-D-aspartate receptor and inhibitory factor kappabeta-alpha within the ipsilateral L5 dorsal root ganglion and spinal cord dorsal horn. Epidural administration of triamcinolone (6.25-100 microg) on postoperative day 3 dose-dependently attenuated both thermal hyperalgesia and mechanical allodynia in rats with chronic compression of lumbar dorsal root ganglion.
The data suggest that this modified rat model of chronic compression of lumbar dorsal root ganglion may be a useful tool to explore the mechanisms as well as new therapeutic options of radicular pain.
神经根性疼痛是一种常见且使人衰弱的临床疼痛病症。迄今为止,神经根性疼痛的机制仍不清楚,部分原因是缺乏合适的临床前模型。作者报告了一种改良的神经根性疼痛大鼠模型,该模型可模拟由背根神经节软组织压迫引起的一部分临床神经根性疼痛病症。
通过向L5椎间孔注入60微升止血基质(SURGIFLO;强生公司,新泽西州萨默维尔)建立神经根性疼痛大鼠模型,导致腰背根神经节慢性受压。在有或没有用曲安奈德进行硬膜外治疗的情况下,测量热痛觉过敏和机械性异常性疼痛。采用蛋白质免疫印迹法评估受影响的L5背根神经节和脊髓背角内N-甲基-D-天冬氨酸受体NR1亚基和炎症标志物抑制因子κBα的表达。
腰背根神经节慢性受压导致:(1)术后持续4或5周出现持续性机械性异常性疼痛和热痛觉过敏;(2)同侧L5背根神经节和脊髓背角内N-甲基-D-天冬氨酸受体和抑制因子κBα上调。术后第3天硬膜外注射曲安奈德(6.25 - 100微克)可剂量依赖性减轻腰背根神经节慢性受压大鼠的热痛觉过敏和机械性异常性疼痛。
数据表明,这种改良的腰背根神经节慢性受压大鼠模型可能是探索神经根性疼痛机制以及新治疗方法的有用工具。