Inositol trisphosphate-dependent periodic activation of a Ca(2+)-activated K+ conductance in glucose-stimulated pancreatic beta-cells

Nature. 1991 Oct 31;353(6347):849-52. doi: 10.1038/353849a0.


Glucose-stimulated insulin secretion is associated with the appearance of electrical activity in the pancreatic beta-cell. At intermediate glucose concentrations, beta-cell electrical activity follows a characteristic pattern of slow oscillations in membrane potential on which bursts of action potentials are superimposed. The electrophysiological background of the bursting pattern remains unestablished. Activation of Ca(2+)-activated large-conductance K+ channels (KCa channel) has been implicated in this process but seems unlikely in view of recent evidence demonstrating that the beta-cell electrical activity is unaffected by the specific KCa channel blocker charybdotoxin. Another hypothesis postulates that the bursting arises as a consequence of two components of Ca(2+)-current inactivation. Here we show that activation of a novel Ca(2+)-dependent K+ current in glucose-stimulated beta-cells produces a transient membrane repolarization. This interrupts action potential firing so that action potentials appear in bursts. Spontaneous activity of this current was seen only rarely but could be induced by addition of compounds functionally related to hormones and neurotransmitters present in the intact pancreatic islet. K+ currents of the same type could be evoked by intracellular application of GTP, the effect of which was mediated by mobilization of Ca2+ from inositol 1,4,5-trisphosphate (InsP3)-sensitive intracellular Ca2+ stores. These observations suggest that oscillatory glucose-stimulated electrical activity, which is correlated with pulsatile release of insulin, results from the interaction between the beta-cell and intraislet hormones and neurotransmitters. Our data also provide evidence for a close interplay between ion channels in the plasma membrane and InsP3-induced mobilization of intracellular Ca2+ in an excitable cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bucladesine / pharmacology
  • Calcium / pharmacology*
  • Carbachol / pharmacology
  • Cells, Cultured
  • Charybdotoxin
  • Cobalt / pharmacology
  • Electric Conductivity / drug effects
  • Evoked Potentials / drug effects
  • Glucose / pharmacology*
  • Guanosine 5'-O-(3-Thiotriphosphate) / pharmacology
  • Guanosine Triphosphate / pharmacology
  • Inositol 1,4,5-Trisphosphate / physiology*
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / physiology*
  • Membrane Potentials / drug effects
  • Mice
  • Potassium Channels / drug effects
  • Potassium Channels / physiology*
  • Scorpion Venoms / pharmacology
  • Tetraethylammonium
  • Tetraethylammonium Compounds / pharmacology


  • Potassium Channels
  • Scorpion Venoms
  • Tetraethylammonium Compounds
  • Charybdotoxin
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Cobalt
  • Bucladesine
  • Tetraethylammonium
  • Inositol 1,4,5-Trisphosphate
  • Guanosine Triphosphate
  • Carbachol
  • Glucose
  • Calcium