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NaV1.7: A central role in pain
Stephen G Waxman1, Sulayman D Dib-Hajj1
1Department of Neurology, Yale University, New Haven, CT 06520; Center for Neuroscience & Regeneration Research, Yale University, New Haven, CT 06520; Center for Rehabilitation Research, VA Connecticut Healthcare System, West Haven, CT 06516.
Abstract:
Loss of function of sodium channel NaV1.7 produces pain insensitivity. In this issue, Deng et al.1 show that analgesia after NaV1.7 removal or pharmacological blockade is not driven by enkephalin overexpression. These results underscore the essential role, independent of endogenous opioids, of NaV1.7 for nociceptor firing and pain.
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