Concentration-dependent effects of tolbutamide, meglitinide, glipizide, glibenclamide and diazoxide on ATP-regulated K+ currents in pancreatic B-cells

Naunyn Schmiedebergs Arch Pharmacol. 1988 Feb;337(2):225-30. doi: 10.1007/BF00169252.


The influence of the hypoglycemic drugs tolbutamide, meglitinide, glipizide and glibenclamide on ATP-dependent K+ currents of mouse pancreatic B-cells was studied using the whole-cell configuration of the patch-clamp technique. In the absence of albumin, tolbutamide blocked the currents half maximally at 4.1 mumol/l. In the presence of 2 mg/ml albumin half maximal inhibition of the currents was observed at 2.1 mumol/l meglitinide, 6.4 nmol/l glipizide and 4.0 nmol/l glibenclamide. The hyperglycemic sulfonamide diazoxide opened ATP-dependent K+ channels. Half maximally effective concentrations of diazoxide were 20 mumol/l with 0.3 mmol/l ATP and 102 mumol/l with 1 mmol/l ATP in the recording pipette. Thus, the action of diazoxide was dependent on the presence of ATP in the recording pipette. The free concentrations of the drugs which influenced ATP-dependent K+ currents were comparable with the free plasma concentrations in humans and the free concentrations which affected insulin secretion in vitro. The results support the view that the target for the actions of sulfonylureas and of diazoxide is the ATP-dependent K+ channel of the pancreatic B-cell or a structure closely related to this channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / physiology*
  • Animals
  • Benzamides / pharmacology
  • Diazoxide / pharmacology*
  • Glipizide / pharmacology
  • Glyburide / pharmacology
  • Hypoglycemic Agents / pharmacology
  • In Vitro Techniques
  • Ion Channels / drug effects*
  • Islets of Langerhans / drug effects*
  • Mice
  • Mice, Inbred Strains
  • Potassium / physiology
  • Sulfonylurea Compounds / pharmacology*
  • Tolbutamide / pharmacology


  • Benzamides
  • Hypoglycemic Agents
  • Ion Channels
  • Sulfonylurea Compounds
  • Adenosine Triphosphate
  • meglitinide
  • Tolbutamide
  • Diazoxide
  • Potassium
  • Glyburide
  • Glipizide