Modulation of transient outward current by extracellular protons and Cd2+ in rat and human ventricular myocytes

J Physiol. 1998 Sep 15;511 ( Pt 3)(Pt 3):827-36. doi: 10.1111/j.1469-7793.1998.827bg.x.

Abstract

1. The effects of extracellular acidosis and Cd2+ on the transient outward current (Ito) have been investigated in rat and human ventricular myocytes, using the whole-cell patch-clamp technique. 2. In rat myocytes, exposure to acidic extracellular solution (pH 6.0) shifted both steady-state activation and inactivation curves to more positive potentials, by 20.5 +/- 2.7 mV (mean +/- S.E.M.; n = 4) and 19.8 +/- 1.2 mV, respectively. Cd2+ also shifted the activation and inactivation curves in a positive direction in a concentration-dependent manner. 3. In human myocytes, the steady-state activation and inactivation curves were located at more positive potentials. The effect of Cd2+ was similar, but acidosis had less effect than in rat myocytes (e.g. pH 6.0 shifted activation by only 7.2 +/- 2.2 mV and inactivation by 13.7 +/- 0.5 mV; n = 4). 4. In both species, the effect of acidosis decreased with increasing concentrations of Cd2+ and vice versa, suggesting competition between H+ and Cd2+ for a common binding site. 5. The data indicate that acidosis and divalent cations influence Ito via a similar mechanism and act competitively in both rat and human myocytes, but that human cells are less sensitive to the effects of acidosis.

Publication types

  • Comparative Study

MeSH terms

  • Acidosis / metabolism
  • Acids / pharmacology
  • Animals
  • Binding, Competitive / physiology
  • Cadmium / pharmacology*
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels / physiology
  • Cations, Divalent / pharmacology
  • Female
  • Heart Ventricles / chemistry
  • Heart Ventricles / cytology
  • Humans
  • Hydrogen-Ion Concentration
  • Kinetics
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Middle Aged
  • Muscle Fibers, Skeletal / chemistry*
  • Muscle Fibers, Skeletal / physiology*
  • Myocardium / chemistry
  • Myocardium / cytology*
  • Nisoldipine / pharmacology
  • Patch-Clamp Techniques
  • Protons*
  • Rats

Substances

  • Acids
  • Calcium Channel Blockers
  • Calcium Channels
  • Cations, Divalent
  • Protons
  • Cadmium
  • Nisoldipine