Mg(2+)-dependent inhibition of KATP by sulphonylureas in CRI-G1 insulin-secreting cells

Br J Pharmacol. 1994 Feb;111(2):632-40. doi: 10.1111/j.1476-5381.1994.tb14783.x.

Abstract

1 Patch-clamp recording techniques were used to examine the effects of tolbutamide, glibenclamide, meglitinide and thiopentone on KATP in CRI-GI insulin-secreting cells in the presence and absence of Mg2+. 2 In the absence of Mg2+ in the intracellular bathing solution, tolbutamide was significantly less effective when applied either to the intracellular or to the extracellular surfaces of cell-free patches. Removal of extracellular Mg2+ did not alter the effectiveness of tolbutamide provided that Mg2+ was present at the intracellular surface of the patch. 3 Tolbutamide was also significantly less effective when applied to the intracellular surface of cell-free patches when Mn2+ was used as a replacement for Mg2+. 4 Both the sulphonylurea, glibenclamide and the non-sulphonylurea derivative, meglitinide also showed Mg2+ dependent inhibitory effects in cell-free patches. In contrast, the barbiturate thiopentone inhibited KATP in a Mg(2+)-independent manner. 5 Whole-cell IK(ATP) were used to quantify the effects of tolbutamide and glibenclamide in the presence and absence of intracellular Mg2+. Concentration-inhibition curves, in the presence of intracellular Mg2+, resulted in IC50 values of 12.1 microM and 2.1 nM for tolbutamide and glibenclamide, respectively. In the absence of intracellular Mg2+, the corresponding IC50 values were 25.3 mM and 3.6 microM, respectively. The values of IC50 for thiopentone in the presence and absence of intracellular Mg2+ were 69.4 microM and 69.2 microM, respectively. 6 With respect to the high affinity binding sites for [3H]-glibenclamide in CRI-G1 membranes, no significant differences were found between the dissociation constants for, or the maximal binding capacities of, [3H]-glibenclamide in the presence or absence of Mg2+. 7. In the CRI-G1 insulin-secreting cell line, it is concluded that intracellular Mg2+ does not influence the affinity of the sulphonylureas for the sulphonylurea receptor but that this ion is critically important for the interaction between the sulphonylurea receptor and KATP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / physiology*
  • Animals
  • Benzamides / pharmacology
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Electrophysiology
  • Glyburide / pharmacokinetics
  • Glyburide / pharmacology
  • Hypoglycemic Agents / pharmacology
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / metabolism*
  • Ligands
  • Magnesium / physiology*
  • Potassium Channels / drug effects*
  • Rats
  • Sulfonylurea Compounds / pharmacology*
  • Thiopental / pharmacology
  • Tolbutamide / pharmacology

Substances

  • Benzamides
  • Hypoglycemic Agents
  • Ligands
  • Potassium Channels
  • Sulfonylurea Compounds
  • Adenosine Triphosphate
  • meglitinide
  • Tolbutamide
  • Magnesium
  • Thiopental
  • Glyburide