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哮喘药物伊布地特在周围和中枢神经性疼痛大鼠模型中的抗伤害作用。

The antinociceptive effect of the asthma drug ibudilast in rat models of peripheral and central neuropathic pain.

机构信息

The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.

出版信息

J Neurotrauma. 2012 Feb 10;29(3):600-10. doi: 10.1089/neu.2011.1863. Epub 2011 Oct 19.

Abstract

Ibudilast, an asthma drug, has demonstrated antinociceptive effects in several rat models of peripheral neuropathic pain, and a proposed mechanism of action is the inhibition of release of the cytokine tumor necrosis factor-α (TNF-α) from activated spinal microglia. Spinal glial activation has also been demonstrated in rat models of central neuropathic pain following spinal cord injury (SCI). The current study evaluated the effect of a short course of treatment with ibudilast on SCI-induced pain, and for comparison, following a chronic constriction injury (CCI; the Bennett model) of the sciatic nerve in rats. The effects of ibudilast treatment on spinal (SCI and CCI rats), and nerve tissue (CCI only) TNF-α content were also evaluated. Following an acute midthoracic SCI with a microvascular clip (20-g force), hindpaw withdrawal thresholds were significantly decreased, indicating below-level cutaneous tactile hypersensitivity. Likewise, unilateral loose ligation of the sciatic nerve led to a robust ipsilateral tactile hypersensitivity. Rats were treated with either ibudilast (10 mg/kg IP) or vehicle (2 mL/kg) during the period of robust and steady hindpaw hypersensitivity for each model--CCI rats were treated 14-16 days post-surgery, and SCI rats were treated 30-32 days post-surgery--and tested daily. Ibudilast ameliorated hindpaw hypersensitivity in both SCI and CCI rats, whereas vehicle treatment had no effect. Interestingly, repeated treatment led to increased baseline thresholds, beyond the duration of the drug half-life, suggesting persistent changes in neuropathic pain processing. In SCI rats, an increase in TNF-α content in spinal tissue rostral to the SCI was observed. Ibudilast treatment did not significantly alter this increase. In rats with a CCI, TNF-α content was markedly increased in the ipsilateral sciatic nerve and was partially reduced following ibudilast, but not vehicle, treatment. Ibudilast could be useful for the treatment of neuropathic pain of central as well as peripheral origin.

摘要

异丁司特,一种哮喘药物,在几种外周神经性疼痛的大鼠模型中表现出镇痛作用,其作用机制之一是抑制激活的脊髓小胶质细胞释放细胞因子肿瘤坏死因子-α(TNF-α)。脊髓神经胶质细胞的激活也在脊髓损伤(SCI)后的大鼠中枢神经性疼痛模型中得到了证实。本研究评估了短期使用异丁司特治疗 SCI 诱导的疼痛的效果,并进行了比较,即在大鼠坐骨神经慢性缩窄性损伤(CCI;Bennett 模型)后进行了比较。还评估了异丁司特治疗对脊髓(SCI 和 CCI 大鼠)和神经组织(仅 CCI)TNF-α含量的影响。通过微血管夹(20 克力)进行急性中胸 SCI 后,后爪撤回阈值显著降低,表明低于水平的皮肤触觉过敏。同样,单侧坐骨神经疏松结扎导致同侧触觉过敏明显增强。CCI 大鼠在手术后 14-16 天,SCI 大鼠在手术后 30-32 天接受治疗,每天接受治疗。CCI 大鼠接受异丁司特(10mg/kg IP)或载体(2ml/kg)治疗,以治疗每种模型中稳健且稳定的后爪过敏期,而 SCI 大鼠则接受治疗。异丁司特改善了 SCI 和 CCI 大鼠的后爪过敏,而载体治疗则没有效果。有趣的是,重复治疗导致基线阈值增加,超过药物半衰期的持续时间,表明神经病理性疼痛处理的持续变化。在 SCI 大鼠中,观察到 SCI 上方脊髓组织中 TNF-α含量增加。异丁司特治疗并没有显著改变这种增加。在 CCI 大鼠中,同侧坐骨神经中 TNF-α含量明显增加,并且在接受异丁司特治疗后部分减少,但接受载体治疗后没有减少。异丁司特可能对中枢和周围起源的神经性疼痛的治疗有用。

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