Winkelstein Beth A, DeLeo Joyce A
Department of Anesthesiology, Dartmouth, Hitchcock Medical Center, Lebanon, NH 03756, USA.
Brain Res. 2002 Nov 29;956(2):294-301. doi: 10.1016/s0006-8993(02)03560-6.
Nerve root deformation magnitude affects behavioral sensitivity and spinal cytokine expression in a lumbar radiculopathy model. Despite evidence suggesting spinal glia play a role in persistent pain, no study has examined the relationship between injury severity in painful radiculopathy and spinal glial activation. This study quantified local in vivo biomechanics for nerve root injury, describing effects on temporal glial activation. Sham rats had only nerve root exposure; ligation rats received a tight L5 nerve root ligation with silk suture. Using image analysis, the magnitude of nerve root compressive strain was calculated at the time of injury. Mechanical allodynia was assessed from days 1 to 14 following injury and spinal microglial and astrocytic expression were evaluated using immunohistochemistry on days 1, 3, 7, and 14. More severe ligations produced greater microglial activation, indicating injury severity modulates spinal microglial activation. However, astrocytic activation levels did not demonstrate any relationship with the degree of initial injury severity. While allodynia decreased slightly over time following injury, the temporal changes in mechanical allodynia were not significant. Microglial activation levels were maintained temporally, and in some cases increased over time; whereas, changes in astrocytic activation levels were not temporally or injury-related. While initial nerve root injury severity likely modulates spinal OX-42 (CR3/CD11b) expression, OX-42 staining does not directly correlate with nerve root injury-induced mechanical allodynia.
在腰椎神经根病模型中,神经根变形程度影响行为敏感性和脊髓细胞因子表达。尽管有证据表明脊髓胶质细胞在持续性疼痛中起作用,但尚无研究探讨疼痛性神经根病的损伤严重程度与脊髓胶质细胞激活之间的关系。本研究对神经根损伤的局部体内生物力学进行了量化,描述了其对胶质细胞激活时间的影响。假手术组大鼠仅暴露神经根;结扎组大鼠用丝线对L5神经根进行紧密结扎。通过图像分析,计算损伤时神经根压缩应变的大小。在损伤后第1天至第14天评估机械性异常性疼痛,并在第1天、第3天、第7天和第14天使用免疫组织化学评估脊髓小胶质细胞和星形胶质细胞的表达。更严重的结扎导致更大程度的小胶质细胞激活,表明损伤严重程度可调节脊髓小胶质细胞激活。然而,星形胶质细胞激活水平与初始损伤严重程度之间未显示出任何关系。虽然损伤后随着时间的推移异常性疼痛略有减轻,但机械性异常性疼痛的时间变化并不显著。小胶质细胞激活水平在时间上保持稳定,在某些情况下随时间增加;而星形胶质细胞激活水平的变化与时间或损伤无关。虽然初始神经根损伤严重程度可能调节脊髓OX-42(CR3/CD11b)表达,但OX-42染色与神经根损伤诱导的机械性异常性疼痛无直接相关性。