...
首页> 外文期刊>Journal of neurotrauma >The antinociceptive effect of the asthma drug ibudilast in rat models of peripheral and central neuropathic pain
【24h】

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

机译:哮喘药物异丁司特对周围和中枢神经性疼痛大鼠模型的镇痛作用

获取原文
获取原文并翻译 | 示例

摘要

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.
机译:哮喘药物Ibudilast在几种周围神经性疼痛大鼠模型中均已显示出抗伤害感受的作用,一种拟议的作用机制是抑制活化的脊髓小胶质细胞因子释放的肿瘤坏死因子-α(TNF-α)。在脊髓损伤(SCI)后中枢神经性疼痛的大鼠模型中也已经证明了脊髓神经胶质的激活。当前的研究评估了用异丁司特短疗程对SCI诱发的疼痛的影响,并进行了比较,以比较大鼠坐骨神经的慢性压迫性损伤(CCI; Bennett模型)。还评估了ibudilast治疗对脊髓(SCI和CCI大鼠)和神经组织(仅CCI)TNF-α含量的影响。急性胸中SCI伴有微血管夹(20 g力)后足缩回阈值显着降低,表明皮肤触觉过敏水平低于水平。同样,坐骨神经的单侧松散结扎导致健壮的同侧触觉超敏反应。在健壮和稳定的后爪超敏期间,用异丁司特(10 mg / kg IP)或媒介物(2 mL / kg)治疗大鼠,每只模型CCI大鼠均在手术后14-16天接受治疗,手术后30-32天接受治疗-每天进行测试。 Ibudilast改善了SCI和CCI大鼠的后爪超敏反应,而媒介物治疗无效果。有趣的是,重复治疗导致基线阈值增加,超过了药物半衰期的持续时间,表明神经性疼痛过程持续发生变化。在SCI大鼠中,观察到SCI鼻侧脊柱组织中TNF-α含量的增加。依布地司特治疗并没有明显改变这种增加。在患有CCI的大鼠中,同种坐骨神经中的TNF-α含量显着增加,而在ibudilast而非媒介物治疗后部分降低。伊布地司特可用于治疗中枢性和周围性起源的神经性疼痛。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号