Nociceptive neurons of the dorsal root ganglion (DRG) express a combination of rapidly gating TTX-sensitive and slowly gating TTX-resistant Na currents and the channels that produce these currents have been cloned. The Na_v1.7 and Na_v1.8 channels encode for the rapidly inactivating TTX-sensitive and slowly inactivating TTX-resistant Na currents respectively. Although the Na_v1.7 channel expresses well in cultured mammalian cell lines, attempts to express the Na_v1.8 channel using similar approaches has been met with limited success. The inability to heterologously express Na_v1.8 has hampered detailed characterization of the biophysical properties and pharmacology of these channels. In this study we investigated the determinants of Na_v1.8 expression in tsA201 cells, a transformed variant of HEK293 cells, using a combination of biochemistry, immunochemistry and electrophysiology. Our data indicate that the unusually low expression levels of Nav1.8 in tsA201 cells results from a trafficking defect that traps the channel protein in the endoplasmic reticulum. Incubating the cultured cells with the local anesthetic lidocaine dramatically enhanced the cell surface expression of functional Na_v1.8 channels. The biophysical properties of the heterologously expressed Na_v1.8 channel are similar but not identical to those of the TTX-resistant Na current of native DRG neurons, recorded under similar conditions. Our data indicates that the lidocaine acts as a molecular chaperone that promotes efficient trafficking and increased cell surface expression of Na_v1.8 channels.