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-subunits: therapeutic implications for
pain?*
Department of Pharmacology, The University of Michigan, Ann Arbor, Michigan 48109-0632
Voltage-gated sodium channel
-subunits have been shown
to be key mediators of the pathophysiology of pain. The present review considers the role of sodium channel auxiliary
-subunits in channel modulation, channel protein expression levels, and interactions with
extracellular matrix and cytoskeletal signaling molecules. Although
-subunits have not yet been directly implicated in pain mechanisms,
their intimate association with and ability to regulate
-subunits
predicts that they may be a viable target for therapeutic intervention
in the future. It is proposed that multifunctional sodium channel
-subunits provide a critical link between extracellular and
intracellular signaling molecules and thus have the ability to fine
tune channel activity and electrical excitability.
cell adhesion molecules; extracellular matrix
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