Kato Kinshi, Kikuchi Shin-ichi, Konno Shin-ichi, Sekiguchi Miho
Department of Orthopaedic Surgery, Fukushima Medical University School of Medicine, Fukushima City, Japan.
Spine (Phila Pa 1976). 2008 May 20;33(12):1330-6. doi: 10.1097/BRS.0b013e318173298b.
The role of 5-hydroxytryptamine (5-HT) in sciatica in lumbar disc herniation (LDH) in rats was investigated.
We evaluated the effects of exogenous 5-HT applied on the nerve root on pain-related behavior, the release of endogenous 5-HT in plasma, and the expression of 5-HT2A receptors in dorsal root ganglion (DRG) in a rat LDH model.
In previous studies, 5-HT2A receptor antagonists improved sciatica in patients with LDH and attenuated pain-related behavior induced by nucleus pulposus applied to the nerve root in rats.
Adult female Sprague-Dawley rats were divided into four experimental groups [control group; low-dose (10 microg) 5-HT-group; high-dose (30 microg) 5-HT-group; and autologous nucleus pulposus (NP) and saline group] and each drug was applied to the L5 nerve root. Von Frey tests were used for pain-behavior testing. To assess levels of endogenous 5-HT released in capillaries surrounding inflamed nerve roots, we measured 5-hydroxyindole acetic acid (5-HIAA), a metabolite of 5-HT. Expression of 5-HT2A receptors in the left L5 DRG was examined by immunohistochemical and immunoblotting analyses in the control and NP groups.
Mechanical withdrawal thresholds of the high-dose 5-HT and the NP groups were significantly decreased after surgery compared with the control group and recovered after 14 days in the high-dose 5-HT group. 5-HIAA in plasma was increased by nucleus pulposus applied on the nerve root for 7 days after surgery. The expression of 5-HT2A receptors was enhanced in a time-dependent manner by nucleus pulposus.
Exogenous 5-HT to the nerve root induced pain-related behavior with short-lasting effects compared with the nucleus pulposus application. 5-HIAA content in plasma and expression of 5-HT2A receptors in DRG neurons increased early time points after the nucleus pulposus application. These results suggest that 5-HT plays a role in the early phase of the chemical pathogenesis of sciatica in LDH in rats.
研究5-羟色胺(5-HT)在大鼠腰椎间盘突出症(LDH)所致坐骨神经痛中的作用。
在大鼠LDH模型中,我们评估了外源性5-HT作用于神经根对疼痛相关行为、血浆中内源性5-HT释放以及背根神经节(DRG)中5-HT2A受体表达的影响。
在先前的研究中,5-HT2A受体拮抗剂改善了LDH患者的坐骨神经痛,并减轻了将髓核应用于大鼠神经根所诱导的疼痛相关行为。
成年雌性Sprague-Dawley大鼠分为四个实验组[对照组;低剂量(10微克)5-HT组;高剂量(30微克)5-HT组;自体髓核(NP)和生理盐水组],每种药物均作用于L5神经根。采用von Frey试验进行疼痛行为测试。为评估炎症神经根周围毛细血管中释放的内源性5-HT水平,我们检测了5-HT的代谢产物5-羟吲哚乙酸(5-HIAA)。通过免疫组织化学和免疫印迹分析检测对照组和NP组左侧L5 DRG中5-HT2A受体的表达。
与对照组相比,高剂量5-HT组和NP组术后机械性撤针阈值显著降低,高剂量5-HT组术后14天恢复。髓核作用于神经根7天后,血浆中5-HIAA升高。髓核使5-HT2A受体的表达呈时间依赖性增强。
与应用髓核相比,外源性5-HT作用于神经根诱导的疼痛相关行为持续时间较短。髓核应用后早期血浆中5-HIAA含量及DRG神经元中5-HT2A受体表达增加。这些结果表明5-HT在大鼠LDH所致坐骨神经痛化学发病机制的早期阶段起作用。