Involvement of Na+ channels in pain pathways

被引:168
作者
Baker, MD [1 ]
Wood, JN [1 ]
机构
[1] UCL, Dept Biol, London WC1E 6BT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/S0165-6147(00)01585-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Voltage-dependent Na+ channels in sensory nerves contribute to the control of membrane excitability and underlie action potential generation. Na+ channel subtypes exhibit a neurone-specific and developmentally regulated pattern of expression, and changes in both channel expression and function are caused by disease. Recent evidence implicates specific roles for Na+ channel subtypes Na(v)1.3 and Na(v)1.8 in pain states that are associated with nerve injury and inflammation, respectively. Insight into the role of Na(v)1.8 in pain pathways has been gained by the generation of a null mutant. Although drugs discriminate poorly between subtypes, the molecular diversity of channels and subtype-specific modulation might provide opportunities to target pain pathways selectively.
引用
收藏
页码:27 / 31
页数:5
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