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Articles in PresS, published online ahead of print May 29, 2002
Am J Physiol Cell Physiol, 10.1152/ajpcell.00359.2001
Submitted on July 27, 2001
Accepted on May 20, 2002
1 Physiology, University of Western Ontario, London, Ontario, Canada
2 Physiology, University of Western Ontario, London, Ontario, Canada; Medicine, University of Western Ontario, London, Ontario, Canada; Lawson Health Research Institute, London, Ontario, Canada
3 Medicine, University of Western Ontario, London, Ontario, Canada; Lawson Health Research Institute, London, Ontario, Canada
* To whom correspondence should be addressed. E-mail: stephen.sims{at}fmd.uwo.ca.
Smooth muscle contraction is critical to peristalsis in the human esophagus, yet the nature of the channels mediating excitation remains to be elucidated. The objective of this study was to characterize the inward currents in human esophageal smooth muscle cells (HESMCs). Esophageal tissue was isolated from patients undergoing surgery for cancer, grown in primary culture, and currents were recorded using patch-clamp electrophysiology. Depolarization elicited inward current consisting of transient and sustained components, activating positive to -40 mV and peaking at 0 mV. Conductance was half-activated at -16 mV and half-inactivated at -67 mV. The transient current was abolished by removal of bath Na+ or application of tetrodotoxin (IC50~20 nM), whereas it persisted in the absence of bath Ca2+ or the presence of Cd2+. These data provide evidence that cultured HESMCs express voltage-dependent Na+ channels. RT-PCR revealed mRNA transcripts for Nax, the "atypical" isoform, as well as Nav1.4. These studies provide the first evidence of Nav1.4 in smooth muscle, and contribute to a model of excitation in HESMCs.
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