Phosphorylation-dependent differences in the activation properties of distal and proximal dendritic Na+ channels in rat CA1 hippocampal neurons

J Physiol. 2002 Jun 15;541(Pt 3):665-72. doi: 10.1113/jphysiol.2002.020503.

Abstract

At distal dendritic locations, the threshold for action potential generation is higher and the amplitude of back-propagating spikes is decreased. To study whether these characteristics depend upon Na+ channels, their voltage-dependent properties at proximal and distal dendritic locations were compared in CA1 hippocampal neurons. Distal Na+ channels activated at more hyperpolarized voltages than proximal (half-activation voltages were -20.4 +/- 2.4 mV vs. -12.0 +/- 1.7 mV for distal and proximal patches, respectively, n = 16, P < 0.01), while inactivation curves were not significantly different. The resting membrane potential of distal regions also appeared to be slightly but consistently more hyperpolarized than their proximal counterpart. Staurosporine, a non-selective protein kinase inhibitor, shifted the activation curves for both proximal and distal Na+ channels to the left so that they overlapped and also caused the resting potentials to be comparable. Staurosporine affected neither the inactivation kinetics of Na+ currents nor the reversal potential for Na+. These results suggest that the difference in the voltage dependence of activation of distal and proximal Na+ channels can be attributed to a different phosphorylation state at the two locations.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Algorithms
  • Animals
  • Axons / physiology
  • Dendrites / physiology*
  • Electrophysiology
  • Enzyme Inhibitors / pharmacology
  • Hippocampus / cytology
  • Hippocampus / physiology*
  • In Vitro Techniques
  • Membrane Potentials / physiology
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Phosphorylation*
  • Protein Kinase Inhibitors
  • Rats
  • Rats, Sprague-Dawley
  • Sodium Channels / physiology*
  • Staurosporine / pharmacology

Substances

  • Enzyme Inhibitors
  • Protein Kinase Inhibitors
  • Sodium Channels
  • Staurosporine