Channelpedia

PubMed 20146699


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Nav1.7



Title: Familial pain syndromes from mutations of the NaV1.7 sodium channel.

Authors: Tanya Z Fischer, Stephen G Waxman

Journal, date & volume: Ann. N. Y. Acad. Sci., 2010 Jan , 1184, 196-207

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20146699


Abstract
The literature currently suggests that voltage-gated sodium channels play a major role in the pathogenesis of neuropathic pain. Alterations in the expression and targeting of specific sodium channels within injured dorsal root ganglia neurons appear to predispose the neurons to abnormal firing properties, allowing for the development of neuropathic pain. Mutations of one particular sodium channel (Na(v)1.7) have been shown to cause inherited neuropathic pain in humans, specifically in erythromelalgia and paroxysmal extreme pain disorder. Inherited erythromelalgia is the first human pain syndrome to be understood at a molecular level, having been linked to gain-of-function mutations of Na(v)1.7. Conversely, a loss-of-function of the Na(v)1.7 channel can produce channelopathy-associated insensitivity to pain. Therefore, the Na(v)1.7 channel may provide a unique target for the pharmacotherapy of pain in humans. In this review article we summarize current knowledge regarding several different disease manifestations arising from changes within the Na(v)1.7 channel.