Intrinsic membrane properties underlying spontaneous tonic firing in neostriatal cholinergic interneurons

J Neurosci. 2000 Nov 15;20(22):8493-503. doi: 10.1523/JNEUROSCI.20-22-08493.2000.

Abstract

Neostriatal cholinergic interneurons produce spontaneous tonic firing in the absence of synaptic input. Perforated patch recording and whole-cell recording combined with calcium imaging were used in vitro to identify the intrinsic membrane properties underlying endogenous excitability. Spontaneous firing was driven by the combined action of a sodium current and the hyperpolarization-activated cation current (I(h)), which together ensured that there was no zero current point in the subthreshold voltage range. Blockade of sodium channels or I(h) established a stable subthreshold resting membrane potential. A tetrodotoxin-sensitive region of negative slope conductance was observed between approximately -60 mV and threshold (approximately -50 mV) and the h-current was activated at all subthreshold voltages. Calcium imaging experiments revealed that there was minimal calcium influx at subthreshold membrane potentials but that action potentials produced elevations of calcium in both the soma and dendrites. Spike-triggered calcium entry shaped the falling phase of the action potential waveform and activated calcium-dependent potassium channels. Blockade of big-conductance channels caused spike broadening. Application of apamin, which blocks small-conductance channels, abolished the slow spike afterhyperpolarization (AHP) and caused a transition to burst firing. In the absence of synaptic input, a range of tonic firing patterns are observed, suggesting that the characteristic spike sequences described for tonically active cholinergic neurons (TANs) recorded in vivo are intrinsic in origin. The pivotal role of the AHP in regulating spike patterning indicates that burst firing of TANs in vivo could arise from direct or indirect modulation of the AHP without requiring phasic synaptic input.

Publication types

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

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Animals
  • Apamin / pharmacology
  • Calcium / metabolism
  • Calcium Channel Blockers / pharmacology
  • Cell Membrane / metabolism*
  • Female
  • In Vitro Techniques
  • Interneurons / cytology
  • Interneurons / metabolism*
  • Large-Conductance Calcium-Activated Potassium Channels
  • Male
  • Neostriatum / cytology
  • Neostriatum / metabolism*
  • Patch-Clamp Techniques
  • Potassium Channel Blockers
  • Potassium Channels*
  • Potassium Channels, Calcium-Activated*
  • Rats
  • Rats, Sprague-Dawley
  • Sensory Thresholds / drug effects
  • Sensory Thresholds / physiology
  • Small-Conductance Calcium-Activated Potassium Channels
  • Sodium / metabolism
  • Sodium Channel Blockers
  • Sodium Channels / metabolism
  • Tetrodotoxin / pharmacology

Substances

  • Calcium Channel Blockers
  • Large-Conductance Calcium-Activated Potassium Channels
  • Potassium Channel Blockers
  • Potassium Channels
  • Potassium Channels, Calcium-Activated
  • Small-Conductance Calcium-Activated Potassium Channels
  • Sodium Channel Blockers
  • Sodium Channels
  • Apamin
  • Tetrodotoxin
  • Sodium
  • Calcium