Takahashi Masahiro, Kawaguchi Masahiko, Shimada Keiji, Konishi Noboru, Furuya Hitoshi, Nakashima Toshikatsu
Department of Anesthesiology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Neurosci Lett. 2004 Jun 17;363(3):203-6. doi: 10.1016/j.neulet.2004.03.040.
Recent evidence suggested that cyclooxygenase-2 (COX-2) expression in the peripheral nerve early after nerve injury might be involved in the development of neuropathic pain. Although previous investigators have demonstrated that COX-2 is expressed in peripheral nerve at a late phase (2-4 weeks) after nerve injury, COX-2 up-regulation at an early phase after nerve injury has not been determined. Using immunohistochemistry, we observed biphasic increases of COX-2 expression after L5 single spinal nerve injury. The first increment of COX-2 positive cells was noted 1 day after nerve injury and these cells co-expressed the Schwann cell marker S-100. A second increment was noted after 7-14 days and these cells co-expressed the macrophage marker ED-1. These results suggested that the cellular sources of COX-2 expression might be different between the early and late phases after nerve injury.
最近的证据表明,神经损伤后早期外周神经中环氧合酶-2(COX-2)的表达可能与神经性疼痛的发生有关。尽管先前的研究人员已经证明COX-2在神经损伤后的晚期(2-4周)在外周神经中表达,但神经损伤后早期COX-2的上调情况尚未确定。我们使用免疫组织化学方法观察了L5单根脊神经损伤后COX-2表达的双相增加。COX-2阳性细胞的第一次增加在神经损伤后1天被注意到,这些细胞同时表达雪旺细胞标志物S-100。第二次增加在7-14天后被注意到,这些细胞同时表达巨噬细胞标志物ED-1。这些结果表明,神经损伤后早期和晚期COX-2表达的细胞来源可能不同。