Kv7 channels a potential therapeutic target in fibromyalgia: A hypothesis

K. Lawson
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引用次数: 8

Abstract

Fibromyalgia is characterized by the primary symptoms of persistent diffuse pain, fatigue, sleep disturbance and cognitive dysfunction. Persistent pain conditions, such as fibromyalgia, are often refractory to current available therapies. An involvement of K+ channels in the pathophysiology of fibromyalgia is emerging and supported by drug treatments for this condition exhibiting action at these molecular processes. K+ channels constitute potential novel target candidates for pain therapy offering peripheral and/or central actions. The Kv7 channel activators, flupirtine and retigabine, have exhibited pharmacological profiles compatible to the requirements needed for use as a therapeutic approach to fibromyalgia. Clinical trials to address the multidimensional challenges of fibromyalgia with flupirtine and retigabine will provide important insight to the role of K+ channels in this condition.
Kv7通道是纤维肌痛的潜在治疗靶点:一种假设
纤维肌痛的主要症状是持续性弥漫性疼痛、疲劳、睡眠障碍和认知功能障碍。持续性疼痛,如纤维肌痛,通常对现有的治疗方法是难治的。K+通道参与纤维肌痛的病理生理正在出现,并得到药物治疗的支持,这些药物治疗在这些分子过程中表现出作用。K+通道是疼痛治疗的潜在新靶点,提供外周和/或中枢作用。Kv7通道激活剂氟吡汀和瑞加滨已显示出符合纤维肌痛治疗要求的药理学特征。使用氟吡汀和瑞加滨治疗纤维肌痛的临床试验将为K+通道在这种情况下的作用提供重要的见解。
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