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Neuropathic Pain After Spinal Cord Injury: Challenges and Research Perspectives

机译:脊髓损伤后的神经性疼痛:挑战和研究前景。

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摘要

Neuropathic pain is a debilitating consequence of spinal cord injury (SCI) that remains difficult to treat because underlying mechanisms are not yet fully understood. In part, this is due to limitations of evaluating neuropathic pain in animal models in general, and SCI rodents in particular. Though pain in patients is primarily spontaneous, with relatively few patients experiencing evoked pains, animal models of SCI pain have primarily relied upon evoked withdrawals. Greater use of operant tasks for evaluation of the affective dimension of pain in rodents is needed, but these tests have their own limitations such that additional studies of the relationship between evoked withdrawals and operant outcomes are recommended. In preclinical SCI models, enhanced reflex withdrawal or pain responses can arise from pathological changes that occur at any point along the sensory neuraxis. Use of quantitative sensory testing for identification of optimal treatment approach may yield improved identification of treatment options and clinical trial design. Additionally, a better understanding of the differences between mechanisms contributing to at- versus below-level neuropathic pain and neuropathic pain versus spasticity may shed insights into novel treatment options. Finally, the role of patient characteristics such as age and sex in pathogenesis of neuropathic SCI pain remains to be addressed.Electronic supplementary materialThe online version of this article (10.1007/s13311-018-0633-4) contains supplementary material, which is available to authorized users.
机译:神经性疼痛是脊髓损伤(SCI)的一种令人衰弱的后果,由于尚未完全了解其潜在机制,因此仍然难以治疗。部分原因是由于通常在动物模型中,尤其是在SCI啮齿动物中评估神经性疼痛的局限性。尽管患者的疼痛主要是自发的,很少有患者出现诱发性疼痛,但SCI疼痛的动物模型主要依赖于诱发性戒断。需要更多地使用操作任务来评估啮齿动物疼痛的情感程度,但是这些测试有其自身的局限性,因此建议对诱发的戒断与操作结果之间的关系进行其他研究。在临床前SCI模型中,增强的反射性退缩或疼痛反应可能是由于沿感觉神经的任何位置发生的病理变化引起的。使用定量感官测试确定最佳治疗方法可能会改善治疗选择和临床试验设计的识别。此外,更好地了解导致水平以下和以下水平的神经性疼痛的机制与神经性疼痛与痉挛的机制之间的差异可能会为新的治疗选择提供见识。最后,患者特征(如年龄和性别)在神经性SCI疼痛的发病机理中的作用仍有待解决。电子补充材料本文的在线版本(10.1007 / s13311-018-0633-4)包含补充材料,可用于授权用户。

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