Centre for Neurosciences Studies, 18, Stuart Street, Queen's University, Kingston, Ontario K7L 3N6, Canada.
J Neuroinflammation. 2010 Apr 16;7:27. doi: 10.1186/1742-2094-7-27.
Tumor necrosis factor alpha (TNF-alpha) was discovered more than a century ago, and its known roles have extended from within the immune system to include a neuro-inflammatory domain in the nervous system. Neuropathic pain is a recognized type of pathological pain where nociceptive responses persist beyond the resolution of damage to the nerve or its surrounding tissue. Very often, neuropathic pain is disproportionately enhanced in intensity (hyperalgesia) or altered in modality (hyperpathia or allodynia) in relation to the stimuli. At time of this writing, there is as yet no common consensus about the etiology of neuropathic pain - possible mechanisms can be categorized into peripheral sensitization and central sensitization of the nervous system in response to the nociceptive stimuli. Animal models of neuropathic pain based on various types of nerve injuries (peripheral versus spinal nerve, ligation versus chronic constrictive injury) have persistently implicated a pivotal role for TNF-alpha at both peripheral and central levels of sensitization. Despite a lack of success in clinical trials of anti-TNF-alpha therapy in alleviating the sciatic type of neuropathic pain, the intricate link of TNF-alpha with other neuro-inflammatory signaling systems (e.g., chemokines and p38 MAPK) has indeed inspired a systems approach perspective for future drug development in treating neuropathic pain.
肿瘤坏死因子-α(TNF-α)在一个多世纪前被发现,其已知的作用已经从免疫系统扩展到神经系统中的神经炎症领域。神经病理性疼痛是一种公认的病理性疼痛类型,其中伤害性反应持续存在,超过了神经或其周围组织损伤的解决。通常,与刺激相比,神经病理性疼痛的强度(痛觉过敏)或模式(超敏反应或感觉异常)不成比例地增强。在撰写本文时,对于神经病理性疼痛的病因尚未达成共识-可能的机制可以分为外周敏化和中枢敏化对伤害性刺激的神经系统。基于各种类型的神经损伤(周围神经与脊神经、结扎与慢性缩窄性损伤)的神经病理性疼痛动物模型,一直表明 TNF-α在敏化的外周和中枢水平都具有关键作用。尽管在临床试验中抗 TNF-α治疗减轻坐骨神经型神经病理性疼痛的效果不佳,但 TNF-α与其他神经炎症信号系统(例如趋化因子和 p38 MAPK)的复杂联系确实激发了未来治疗神经病理性疼痛的药物开发的系统方法观点。