Review Article

From Acupuncture to Interaction between -Opioid Receptors and Na+ Channels: A Potential Pathway to Inhibit Epileptic Hyperexcitability

Table 2

Voltage-gated sodium channels.

Subunit

SubtypesNav1.1–Nav1.9 1– 4

LocationPrevalent in the CNS: Two subunits associated with an α subunit
 Nav1.1, Nav1.2, Nav1.3, and Nav1.6
Abundant in muscle:
 Nav1.4, Nav1.5
Primarily in peripheral nervous system:
 Nav1.7, Nav1.8,  and Nav1.9

Cellular distributionPrimary localized in cell body:Expressed in a complementary fashion (either 1 or 3, and 2 or 4) with subunit
 Nav1.1 and Nav1.3
High expression in unmyelinated or pre myelinated axons and
 dendrites:
 Nav1.2
Nodes of Ranvier and axon initial segments as well as in the
 somata and dendrites of many projection neurons:
 Nav1.6

FunctionForms the ion-conducting pore and activation and inactivation gates Modify the kinetics and voltage dependence of gating
Serve as cell adhesion molecules for integrating the channels into the appropriate subcellular domains