Glibenclamide inhibits mitochondrial K+ and Na+ uniports induced by magnesium depletion

Int J Biochem Cell Biol. 1996 Aug;28(8):863-71. doi: 10.1016/1357-2725(96)00040-4.

Abstract

Magnesium depletion induces K+ and Na+ uniports in rat liver mitochondria. The purpose of the present study was to investigate the effects exerted by the antidiabetic sulfonylurea, glibenclamide, a well known blocker of ATP-sensitive potassium channels, on mitochondrial K+ and Na+ uniports. The K+ and Na+ uniport activities were monitored indirectly, in energized mitochondria, by following K+ and Na+ influxes as measured by light scattering. The membrane potential of the mitochondria was determined using a TPP+ selective electrode. Equilibrium binding measurements of glibenclamide to the inner mitochondrial membrane was performed with [3H]glibenclamide. Mitochondrial K+ and Na+ uniports were found to be inhibited by glibenclamide in a concentration-dependent manner, with IC50 of 20 +/- 7 and 15 +/- 8 microM, respectively. On lowering of the pH value, the potency of glibenclamide to inhibit the uniports activity was increased. Binding studies revealed the presence of a single class of low affinity binding sites for glibenclamide in the inner mitochondrial membrane, with a Kd of 4 +/- 2 microM and a BMAX of 148 +/- 50 pmoles/mg of protein. The present study provides evidence that both mitochondrial K+ and Na+ uniport activities are sensitive to the antidiabetic sulfonylurea, glibenclamide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Glyburide / pharmacology*
  • Hydrogen-Ion Concentration
  • Hypoglycemic Agents / pharmacology*
  • Ion Transport / drug effects
  • Magnesium / metabolism*
  • Male
  • Mitochondria, Liver / metabolism*
  • Potassium / metabolism*
  • Rats
  • Rats, Wistar
  • Sodium / metabolism*

Substances

  • Hypoglycemic Agents
  • Sodium
  • Magnesium
  • Potassium
  • Glyburide