Chronic exposure to high glucose and impairment of K(+)-channel function in perifused rat pancreatic islets

Diabetes. 1990 Mar;39(3):397-9. doi: 10.2337/diab.39.3.397.

Abstract

Prolonged exposure to high glucose levels impairs the ability of pancreatic islets to secrete insulin as a response to that stimulus. Because glucose, like other insulin secretagogues, elicits insulin secretion by inhibiting the ATP-sensitive K+ channels, in this study, we investigated the effect of prolonged (24-h) exposure of rat pancreatic islets to high (16.7 mM) glucose concentration on 86Rb efflux (used as a tracer for K+). The data obtained indicate that islets exposed to high glucose concentration have impaired function of the glucose-sensitive K+ channel, this phenomenon is temporarily related to a defective response of glucose-induced insulin release, and these alterations are reversible.

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Cell Membrane Permeability / drug effects
  • Cells, Cultured
  • Glucose / pharmacology*
  • Insulin / metabolism
  • Islets of Langerhans / cytology
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / physiology*
  • Male
  • Potassium / metabolism
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism
  • Potassium Channels / physiology*
  • Rats
  • Rats, Inbred Strains
  • Rubidium Radioisotopes

Substances

  • Insulin
  • Potassium Channels
  • Rubidium Radioisotopes
  • Adenosine Triphosphate
  • Glucose
  • Potassium