Tachihara Hisayoshi, Sekiguchi Miho, Kikuchi Shin-ichi, Konno Shin-ichi
Department of Orthopaedic Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Spine (Phila Pa 1976). 2008 Apr 1;33(7):743-7. doi: 10.1097/BRS.0b013e3181696132.
Experimental animal study.
To determine whether corticosteroids produce additional benefit to nerve root infiltration (NRI) for experimental lumbar disc herniation.
NRI is used for nonsurgical treatment of radicular symptoms caused by lumbar disc herniation or lumbar spinal canal stenosis. Various studies have shown that NRI using local anesthetic or combinations of local anesthetic and corticosteroid can provide both short- and long-term pain relief. However, whether corticosteroids produce additional benefit to NRI remains controversial.
A total of 174 adult female Sprague-Dawley rats were used in this study. The left L5 nerve root and dorsal root ganglion (DRG) were exposed. For the nontreatment group, autologous nucleus pulposus was harvested from the tail and applied to the DRG. For treatment groups, 1% lidocaine (Lido group), 0.4% dexamethasone (Dexa group), 1% lidocaine + 0.4% dexamethasone (Lido + Dexa group), or saline (Saline group) was injected into the underlayer of epineurium just distal to the nucleus pulposus. At 2, 7, 14, and 21 days after surgery, withdrawal threshold was determined using the von Frey test for mechanical allodynia. Expression of tumor necrosis factor (TNF)-alpha in the DRG was examined by immunohistochemical analyses and immunoblotting.
Withdrawal threshold decreased in the nontreatment group from day 2 to day 14. Conversely, Lido, Dexa, and Lido + Dexa groups showed no decreases in withdrawal thresholds, and no significant differences were observed among these 3 groups. Immunohistochemical analyses showed that TNF-alpha was localized in DRG neurons in all groups. Immunoblotting showed that expression of TNF-alpha in the DRG was lower in Lido, Dexa, and Lido + Dexa groups than in the nontreatment group. No significant differences were observed among these 3 groups.
NRI prevented mechanical allodynia. However, no additional benefit from using corticosteroid was identified, suggesting that corticosteroid may be unnecessary for NRI.
实验性动物研究。
确定皮质类固醇激素对实验性腰椎间盘突出症的神经根浸润(NRI)是否产生额外益处。
NRI用于非手术治疗腰椎间盘突出症或腰椎管狭窄症引起的神经根症状。各种研究表明,使用局部麻醉剂或局部麻醉剂与皮质类固醇激素联合进行NRI可提供短期和长期的疼痛缓解。然而,皮质类固醇激素对NRI是否产生额外益处仍存在争议。
本研究共使用174只成年雌性Sprague-Dawley大鼠。暴露左侧L5神经根和背根神经节(DRG)。对于未治疗组,从尾部采集自体髓核并应用于DRG。对于治疗组,将1%利多卡因(利多卡因组)、0.4%地塞米松(地塞米松组)、1%利多卡因+0.4%地塞米松(利多卡因+地塞米松组)或生理盐水(生理盐水组)注射到髓核远端的神经外膜下层。在术后2、7、14和21天使用von Frey试验测定机械性异常性疼痛的撤针阈值。通过免疫组织化学分析和免疫印迹检查DRG中肿瘤坏死因子(TNF)-α的表达。
未治疗组的撤针阈值从第2天到第14天下降。相反,利多卡因组、地塞米松组和利多卡因+地塞米松组的撤针阈值没有下降,且这3组之间未观察到显著差异。免疫组织化学分析显示,TNF-α在所有组的DRG神经元中均有定位。免疫印迹显示,利多卡因组、地塞米松组和利多卡因+地塞米松组DRG中TNF-α的表达低于未治疗组。这3组之间未观察到显著差异。
NRI可预防机械性异常性疼痛。然而,未发现使用皮质类固醇激素有额外益处,提示皮质类固醇激素可能对NRI不必要。