Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Ann Neurol. 2011 Jan;69(1):13-21. doi: 10.1002/ana.22351.
Chronic peripheral neuropathic pain is the result of abnormal activity in sensory nerves. It is well recognized that this sensory nerve dysfunction can be caused by traumatic, toxic, or metabolic insult to the nerve. In addition, there is growing recognition that neuropathic pain is a frequent manifestation of neurodegenerative diseases. In this regard, important clues to the cellular mechanisms of neuropathic pain may be found by close examination of neurodegenerative diseases (including Parkinson's disease) in which neuropathic pain is often an underappreciated but important clinical manifestation. This approach identifies specific mitochondrial and cytoskeletal mechanisms, previously implicated in the pathophysiology of neurodegenerative diseases in the central nervous system, that might contribute to neuropathic dysfunction in peripheral sensory nerve fibers. Investigations in preclinical models of common peripheral neuropathic pain conditions have supported the idea that a subset of these cellular mechanisms of neurodegeneration can produce painful hyperactivity in primary afferent nociceptors. Importantly, this emerging concept of neurodegenerative disease mechanisms in the primary afferent nociceptor identifies novel molecular targets for the treatment neuropathic pain.
慢性周围神经性疼痛是感觉神经异常活动的结果。人们已经充分认识到,这种感觉神经功能障碍可能是由于神经受到创伤、毒性或代谢损伤引起的。此外,人们越来越认识到,神经性疼痛是神经退行性疾病的常见表现。在这方面,通过仔细研究神经性疼痛经常被低估但却是重要临床表现的神经退行性疾病(包括帕金森病),可能会发现神经性疼痛的细胞机制的重要线索。这种方法确定了特定的线粒体和细胞骨架机制,这些机制先前与中枢神经系统神经退行性疾病的病理生理学有关,可能有助于周围感觉神经纤维的神经性功能障碍。对常见周围神经性疼痛疾病的临床前模型的研究支持了这样一种观点,即这些神经退行性疾病的细胞机制的一部分可以在初级传入伤害感受器中产生疼痛性过度活跃。重要的是,这种初级传入伤害感受器中神经退行性疾病机制的新出现概念确定了治疗神经性疼痛的新的分子靶点。