慢性疼痛
药物基因组学
钠通道
神经科学
医学
上瘾
钠通道阻滞剂
神经病理性疼痛
生物信息学
心理学
药理学
生物
钠
化学
有机化学
作者
Sulayman D. Dib‐Hajj,Stephen G. Waxman
标识
DOI:10.1146/annurev-neuro-070918-050144
摘要
Acute pain is adaptive, but chronic pain is a global challenge. Many chronic pain syndromes are peripheral in origin and reflect hyperactivity of peripheral pain-signaling neurons. Current treatments are ineffective or only partially effective and in some cases can be addictive, underscoring the need for better therapies. Molecular genetic studies have now linked multiple human pain disorders to voltage-gated sodium channels, including disorders characterized by insensitivity or reduced sensitivity to pain and others characterized by exaggerated pain in response to normally innocuous stimuli. Here, we review recent developments that have enhanced our understanding of pathophysiological mechanisms in human pain and advances in targeting sodium channels in peripheral neurons for the treatment of pain using novel and existing sodium channel blockers.
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