Mode switching characterizes the activity of large conductance potassium channels recorded from rat cortical fused nerve terminals

J Physiol. 1998 Dec 15;513 ( Pt 3)(Pt 3):733-47. doi: 10.1111/j.1469-7793.1998.733ba.x.

Abstract

1. Inside-out recordings from rat cortical fused nerve terminals indicate that the most common channel observed was a large conductance K+ (BK) channel with characteristics dissimilar to conventional cell body calcium-activated BK (BKCa) channels. 2. BK channels exhibit mode switching between low (mode 1) and high (mode 2) activity, an effect not influenced by membrane voltage. Increasing internal Ca2+ concentration increased time spent in mode 2 as did application of protein kinase A, an effect not mimicked by protein kinase C or protein kinase G. 3. Mode 1 activity was voltage independent although depolarization increased mode 2 channel activity. Global average channel activity was voltage and Ca2+ dependent. 4. Alkaline phosphatase treatment induced channel activity to reside permanently in mode 2, where activity was voltage and Ca2+ dependent but unaffected by protein kinases A, G or C. 5. Internal application of tetraethylammonium blocked BK channel activity in a manner identical to that reported for BKCa channels. 6. These results indicate that nerve terminal membranes have large conductance K+ channels with significant differences in gating kinetics and regulation of activity compared with BKCa channels of other neuronal preparations. The BK channel subtype may play a unique physiological role specific to the nerve terminal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / pharmacology
  • Animals
  • Calcium / physiology
  • Cerebral Cortex / cytology
  • Cerebral Cortex / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Electric Stimulation
  • Electrophysiology
  • Ion Channel Gating / drug effects
  • Male
  • Membrane Potentials / physiology
  • Neurons / metabolism
  • Patch-Clamp Techniques
  • Potassium Channels / metabolism*
  • Presynaptic Terminals / metabolism*
  • Protein Kinase C / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Tetraethylammonium Compounds / pharmacology

Substances

  • Potassium Channels
  • Tetraethylammonium Compounds
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Alkaline Phosphatase
  • Calcium