Inherited erythermalgia: limb pain from an S4 charge-neutral Na channelopathy
Background: Inherited erythermalgia (also termed “erythromelalgia”), characterized by
episodic burning pain in the distal extremities evoked by warmth, has been causally linked
with mutations of the Nav1. 7 sodium channel, which is preferentially expressed in
nociceptors. Thus far, Nav1. 7 mutations within intracellular linker parts of the channel have
been physiologically characterized. Objective: To investigate a Nav1. 7 erythermalgia
mutation that substitutes one uncharged amino acid for another within an S4 segment …
episodic burning pain in the distal extremities evoked by warmth, has been causally linked
with mutations of the Nav1. 7 sodium channel, which is preferentially expressed in
nociceptors. Thus far, Nav1. 7 mutations within intracellular linker parts of the channel have
been physiologically characterized. Objective: To investigate a Nav1. 7 erythermalgia
mutation that substitutes one uncharged amino acid for another within an S4 segment …
Background: Inherited erythermalgia (also termed “erythromelalgia”), characterized by episodic burning pain in the distal extremities evoked by warmth, has been causally linked with mutations of the Nav1.7 sodium channel, which is preferentially expressed in nociceptors. Thus far, Nav1.7 mutations within intracellular linker parts of the channel have been physiologically characterized.
Objective: To investigate a Nav1.7 erythermalgia mutation that substitutes one uncharged amino acid for another within an S4 segment.
Methods: Whole-cell patch-clamp analysis was used to study biophysical properties of wild-type and mutant (F216S) Nav1.7 channels in mammalian cells.
Results: The F216S mutation hyperpolarizes the voltage dependence of activation by 11 mV, accelerates activation, slows deactivation, and enhances the response to slow, small depolarizations.
Conclusion: These results provide a physiologic basis for the linkage to erythermalgia of an Nav1.7 mutation that substitutes one uncharged residue for another within an S4 segment of the channel. These changes should increase excitability of nociceptive dorsal root ganglion neurons in which the mutant channel is present, thus contributing to pain.
American Academy of Neurology