Rao Srinivas G
Cypress Bioscience, Inc., 4350 Executive Drive, Suite 325, San Diego, CA 92121, USA.
Expert Opin Investig Drugs. 2009 Oct;18(10):1479-93. doi: 10.1517/13543780903203771.
Fibromyalgia (FM) is a chronic musculoskeletal pain disorder often associated with fatigue, dyscognition, and sleep disturbances. Recent research advances highlight a critical role for aberrant central pain processing in FM, and, consistent with these data, the first three drugs approved by the FDA for FM over the past 2 years have a predominantly central mode of action. The first drug, pregabalin, may counteract central pain transmission by inhibiting presynaptic release of excitatory neurotransmitters, including substance P and glutamate. The serotonin-norepinephrine reuptake inhibitors duloxetine and milnacipran have been approved more recently and are believed to reduce pain by increasing serotonin and norepinephrine concentrations in descending inhibitory pain pathways. Agents with multiple other mechanisms of action are in development and promise an assortment of therapeutic options for this complex disorder in the near future.
纤维肌痛(FM)是一种慢性肌肉骨骼疼痛疾病,常伴有疲劳、认知障碍和睡眠障碍。最近的研究进展凸显了FM中异常的中枢性疼痛处理的关键作用,并且,与这些数据一致,过去两年中美国食品药品监督管理局(FDA)批准的用于FM的前三类药物主要具有中枢性作用模式。第一种药物普瑞巴林,可能通过抑制包括P物质和谷氨酸在内的兴奋性神经递质的突触前释放来对抗中枢性疼痛传递。5-羟色胺-去甲肾上腺素再摄取抑制剂度洛西汀和米那普明最近已获批准,据信它们通过增加下行抑制性疼痛通路中的5-羟色胺和去甲肾上腺素浓度来减轻疼痛。具有多种其他作用机制的药物正在研发中,有望在不久的将来为这种复杂疾病提供一系列治疗选择。