Aprikalim reduces the Na+-Ca2+ exchange outward current enhanced by hyperkalemia in rat ventricular myocytes

Ann Thorac Surg. 2002 Apr;73(4):1253-9; discussion 1259-60. doi: 10.1016/s0003-4975(02)03381-7.

Abstract

Background: [corrected] Aprikalim, an adenosine triphosphate (ATP) sensitive K+ (K(ATP)) channel opener, attenuates the elevation of intracellular Ca2+ concentration ([Ca2+]i) and improves the contractile functions after hyperkalemic and hypothermic cardioplegia. There is evidence that cardioplegia increases the Na+-Ca2+ exchange activity without affecting Ca2+ influx through L-type Ca2+ channels or Ca2+ content in the sarcoplasmic reticulum, the intracellular Ca2+ store.

Methods: We measured the Na+-Ca2+ exchange outward current with the patch-clamp technique in single rat ventricular myocytes exposed to hyperkalemia and hypothermia in the presence of aprikalim. The intracellular calcium concentration ([Ca2+]i) during cardioplegia, and the contractile function and [Ca2+]i transients induced by electrical stimulation or caffeine during rewarming and reperfusion in single ventricular myocytes were also determined. Contraction and [Ca2+]i were determined with video tracking and spectrofluorometry, respectively.

Results: Aprikalim, 100 micromol/L, the effect of which was blocked by glibamclamide, a K(ATP) inhibitor, significantly attenuated the hyperkalemia-elevated Na+-Ca2+ exchange current by 26% and 11% at 22 degrees C and 4 degrees C, respectively. Aprikalim also attenuated significantly the [Ca2+]i elevated during cardioplegia. Furthermore aprikalim significantly attenuated the reduction in amplitude and prolongation in duration of contraction of myocytes after cardioplegia. The effects of aprikalim mimicked those of nickle (Ni2+), a Na+-Ca2+ exchange blocker. The electrically or caffeine-induced [Ca2+]i transients were unaltered by cardioplegia or aprikalim.

Conclusions: Aprikalim attenuates the Na+-Ca2+ exchange outward current elevated by hyperkalemia, which may attenuate the [Ca2+]i elevation during hyperkalemia and improve the contractile function after cardioplegia in the ventricular myocyte. The study provides further support that addition of a K(ATP) channel opener to the cardioplegic solution may produce beneficial effects in open heart surgery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Calcium / metabolism
  • Glyburide / pharmacology
  • Heart Arrest, Induced
  • Heart Ventricles / cytology*
  • Hyperkalemia / metabolism*
  • Hypothermia, Induced
  • In Vitro Techniques
  • Male
  • Myocardial Contraction
  • Myocardial Reperfusion
  • Myocardium / metabolism*
  • Nickel / pharmacology
  • Patch-Clamp Techniques
  • Picolines / pharmacology*
  • Potassium Channel Blockers
  • Potassium Channels / metabolism
  • Pyrans / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Sodium-Calcium Exchanger / antagonists & inhibitors
  • Sodium-Calcium Exchanger / metabolism*

Substances

  • Picolines
  • Potassium Channel Blockers
  • Potassium Channels
  • Pyrans
  • Sodium-Calcium Exchanger
  • aprikalim
  • Nickel
  • Adenosine Triphosphate
  • Glyburide
  • Calcium