神经病理性疼痛
钠通道
痛觉超敏
钠通道阻滞剂
医学
痛觉过敏
神经科学
感觉系统
麻醉
钠
伤害
内科学
心理学
化学
受体
有机化学
作者
Wen-Ting Shou,Shi‐Hong Zhang,Zhong Chen
出处
期刊:PubMed
日期:2011-03-01
卷期号:40 (2): 217-21
标识
DOI:10.3785/j.issn.1008-9292.2011.02.017
摘要
Voltage-gated sodium channels are critical for the generation and conduction of nerve impulses. Recent studies show that in primary sensory neurons, the expression and dynamic regulation of several sodium channel subtypes play important roles in neuropathic pain. A number of SCN9A (encoding Nav1.7) gene point mutations are related with human genetic pain disorders. Transgenic and specific knockout techniques have revealed that Nav1.3, Nav1.8, Nav1.9 are important for the development and maintenance of neuropathic pain condition. Specific blockers of these sodium channels have been demonstrated to be effective in alleviating allodynia and hyperalgesia. Here we reviewed the roles of sodium channels in neuropathic pain, which may be applicable for the development of new drugs with enhanced efficacy for neuropathic pain treatment.
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