Insulin modulation of intracellular free magnesium in heart: involvement of protein kinase C

Br J Pharmacol. 2000 Jun;130(4):731-8. doi: 10.1038/sj.bjp.0703361.

Abstract

In the present study of rat heart using (31)P-nuclear magnetic resonance, we examined the interaction between beta-adrenergic and insulin receptors in terms of the intracellular free Mg(2+) concentration ([Mg(2+)](i)) regulation. [Mg(2+)](i) was estimated from the separation of the chemical shifts of the alpha- and beta-adenosine triphosphate (ATP) peaks, using the dissociation constant of MgATP 87 microM (established recently). In normal (phosphate-free Krebs-Henseleit) solution, [Mg(2+)](i) was approximately 1.02 mM. Insulin at physiological and pathological concentrations increased [Mg(2+)](i) and contractility in a dose-dependent manner. Insulin (more than 100 micro(u) ml(-1)) suppressed the decrease in [Mg(2+)](i) caused by isoprenaline (100 nM), and these effects of insulin on [Mg(2+)](i) and contractility were blocked by LY333531 (macrocyclic bis (indolyl) maleimide, 100 nM), a protein kinase C (PKC) inhibitor. The isoprenaline-induced decrease in the concentrations of ATP ([ATP]) with insulin application was significantly smaller than that without insulin. Insulin modulates [Mg(2+)](i) and haemodynamics, presumably via activation of PKC, thereby antagonizing the reduction of [Mg(2+)](i) induced by beta-adrenoceptor stimulation.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Calcium Channel Blockers / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Heart / drug effects*
  • Heart / physiology
  • Hemodynamics / drug effects
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Indoles / pharmacology
  • Insulin / pharmacology*
  • Isoproterenol / pharmacology
  • Magnesium / metabolism*
  • Male
  • Maleimides / pharmacology
  • Myocardium / metabolism*
  • Phosphates / metabolism
  • Phosphocreatine / metabolism
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism
  • Rats
  • Rats, Wistar
  • Verapamil / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Calcium Channel Blockers
  • Enzyme Inhibitors
  • Indoles
  • Insulin
  • Maleimides
  • Phosphates
  • Phosphocreatine
  • ruboxistaurin
  • Adenosine Triphosphate
  • Verapamil
  • Protein Kinase C
  • Magnesium
  • Isoproterenol