Na+ channel inactivation: a comparative study between pancreatic islet beta-cells and adrenal chromaffin cells in rat

J Physiol. 2003 Apr 1;548(Pt 1):191-202. doi: 10.1113/jphysiol.2002.034405. Epub 2003 Feb 7.

Abstract

A comparative study was carried out on the inactivation of Na+ channels in two types of endocrine cells in rats, beta-cells and adrenal chromaffin cells (ACCs), using patch-clamp techniques. The beta-cells were very sensitive to hyperpolarization; the Na+ currents increased ninefold when the holding potential was shifted from -70 mV to -120 mV. ACCs were not sensitive to hyperpolarization. The half-inactivation voltages were -90 mV (rat beta-cells) and -62 mV (ACCs). The time constant for recovery from inactivation at -70 mV was 10.5 times slower in beta-cells (60 ms) than in ACCs (5.7 ms). The rate of Na+-channel inactivation at physiological resting potential was more than three times slower in beta-cells than in ACCs. Na+ influx through Na+ channels had no effect on the secretory machinery in rat beta-cells. However, these 'silent Na+ channels' could contribute to the generation of action potentials in some conditions, such as when the cell is hyperpolarized. It is concluded that the fractional availability of Na+ channels in beta-cells at a holding potential of -70 mV is about 15 % of that in ACCs. This value in rat beta-cells is larger than that observed in mouse (0 %), but is smaller than those observed in human or dog (90 %).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Glands / cytology
  • Adrenal Glands / drug effects
  • Adrenal Glands / metabolism*
  • Animals
  • Cells, Cultured
  • Chromaffin Cells / drug effects
  • Chromaffin Cells / metabolism*
  • Electrophysiology
  • Islets of Langerhans / drug effects*
  • Kinetics
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mice
  • Patch-Clamp Techniques
  • Rats
  • Rats, Wistar
  • Sodium Channel Blockers / pharmacology*
  • Tolbutamide / pharmacology

Substances

  • Sodium Channel Blockers
  • Tolbutamide