Sodium channels confer excitability on neurons in nociceptive
pathways and exhibit neuronal tissue specific and injury regulated
expression. This volume provides recent insights into the control
of expression, functioning and membrane trafficking of nervous
system sodium channels and reviews why sodium channel sub-types are
potentially important drug targets in the treatment of pain. The
roles of sodium channels in dental and visceral pain are also
addressed. The emerging role of sodium channel Nav1.3 in
neuropathic states is another important theme.
Authors from the pharmaceutical industry discuss pharmacological
approaches to the drug targeting of sodium channels, and in
particular Nav1.8, exclusively expressed in nociceptive neurons.
The final chapter highlights the functional diversity of sodium
channels in part provided by post-transcriptional processing and
the insights into sodium channel function that are being provided
by tissue specific and inducible gene knock-out technology.
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