Miao G-S, Liu Z-H, Wei S-X, Luo J-G, Fu Z-J, Sun T
Department of Pain Management, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, PR China.
Department of Anesthesiology, The Sixth People's Hospital of Jinan, Zhangqiu, Shandong, PR China.
Neuroscience. 2015 Aug 6;300:10-8. doi: 10.1016/j.neuroscience.2015.04.060. Epub 2015 May 2.
Inflammatory response induced by protrused nucleus pulposus (NP) has been shown to play a crucial role in the process of radicular pain. Lipoxins represent a unique class of lipid mediators that have anti-inflammatory and pro-resolving action. The present study was undertaken to investigate if intrathecal lipoxin A4 (LXA4) could alleviate mechanical allodynia in the rat models of application of NP to the L5 dorsal root ganglion (DRG). Non-compressive models of application of NP to L5 DRG were established and intrathecal catheterization for drug administration was performed in rats. Daily intrathecal injection of vehicle or LXA4 (10ng or 100ng) was performed for three successive days post-operation. Mechanical thresholds were tested and the ipsilateral lumbar (L4-L6) segment of spinal dorsal horns were removed for the determination of tumor necrosis factor-α (TNF-α), IL-1β, transforming growth factor-β1 (TGF-β1) and IL-10 expression and NF-κB/p65, extracellular signal-regulated kinase (ERK), C-Jun N-terminal kinase (JNK) and P38 expression. Application of NP to DRG in rats induced mechanical allodynia, increased the expression of pro-inflammatory factors (TNF-α and IL-1β), NF-κB/p65, the phosphorylated-ERK (p-ERK), -JNK (p-JNK) and -P38 (p-p38) and decreased the expression of anti-inflammatory cytokines (TGF-β1 and IL-10) in the ipsilateral lumbar (L4-L6) segment of spinal dorsal horns. Intrathecal injection of LXA4 alleviated the development of neuropathic pain, inhibited the upregulation of pro-inflammatory cytokines (TNF-α and IL-1β), upregulated the expression of anti-inflammatory cytokines (TGF-β1 and IL-10) and attenuated the activation of NF-κB/p65, p-ERK, p-JNK, but not p-p38, in a dose-dependent manner. In this study, we have demonstrated that LXA4 potently alleviate radicular pain in a rat model of non-compressive lumbar disc herniation. The anti-inflammatory and pro-resolution properties of LXA4 have shown a great promise for the management of radicular pain caused by intervertebral disc herniation.
突出的髓核(NP)诱导的炎症反应已被证明在神经根性疼痛过程中起关键作用。脂氧素是一类独特的脂质介质,具有抗炎和促消退作用。本研究旨在探讨鞘内注射脂氧素A4(LXA4)是否能减轻将NP应用于L5背根神经节(DRG)的大鼠模型中的机械性异常性疼痛。建立了将NP应用于L5 DRG的非压迫性模型,并对大鼠进行鞘内导管插入术以进行药物给药。术后连续三天每天鞘内注射溶剂或LXA4(10 ng或100 ng)。测试机械阈值,并取出脊髓背角的同侧腰段(L4-L6)用于测定肿瘤坏死因子-α(TNF-α)、IL-1β、转化生长因子-β1(TGF-β1)和IL-10的表达以及NF-κB/p65、细胞外信号调节激酶(ERK)、C-Jun氨基末端激酶(JNK)和P38的表达。将NP应用于大鼠的DRG会诱导机械性异常性疼痛,增加促炎因子(TNF-α和IL-1β)、NF-κB/p65、磷酸化ERK(p-ERK)、-JNK(p-JNK)和-P38(p-p38)的表达,并降低脊髓背角同侧腰段(L4-L6)中抗炎细胞因子(TGF-β1和IL-10)的表达。鞘内注射LXA4减轻了神经性疼痛的发展,抑制了促炎细胞因子(TNF-α和IL-1β)的上调,上调了抗炎细胞因子(TGF-β1和IL-10)的表达,并以剂量依赖性方式减弱了NF-κB/p65、p-ERK、p-JNK的激活,但未减弱p-p38的激活。在本研究中,我们证明了LXA4能有效减轻非压迫性腰椎间盘突出症大鼠模型中的神经根性疼痛。LXA4的抗炎和促消退特性为治疗椎间盘突出症引起的神经根性疼痛显示出巨大的前景。