Reduction of an Afterhyperpolarization Current Increases Excitability in Striatal Cholinergic Interneurons in Rat Parkinsonism

J Neurosci. 2011 Apr 27;31(17):6553-64. doi: 10.1523/JNEUROSCI.6345-10.2011.

Abstract

Striatal cholinergic interneurons show tonic spiking activity in the intact and sliced brain, which stems from intrinsic mechanisms. Because of it, they are also known as "tonically active neurons" (TANs). Another hallmark of TAN electrophysiology is a pause response to appetitive and aversive events and to environmental cues that have predicted these events during learning. Notably, the pause response is lost after the degeneration of dopaminergic neurons in animal models of Parkinson's disease. Moreover, Parkinson's disease patients are in a hypercholinergic state and find some clinical benefit in anticholinergic drugs. Current theories propose that excitatory thalamic inputs conveying information about salient sensory stimuli trigger an intrinsic hyperpolarizing response in the striatal cholinergic interneurons. Moreover, it has been postulated that the loss of the pause response in Parkinson's disease is related to a diminution of I(sAHP), a slow outward current that mediates an afterhyperpolarization following a train of action potentials. Here we report that I(sAHP) induces a marked spike-frequency adaptation in adult rat striatal cholinergic interneurons, inducing an abrupt end of firing during sustained excitation. Chronic loss of dopaminergic neurons markedly reduces I(sAHP) and spike-frequency adaptation in cholinergic interneurons, allowing them to fire continuously and at higher rates during sustained excitation. These findings provide a plausible explanation for the hypercholinergic state in Parkinson's disease. Moreover, a reduction of I(sAHP) may alter synchronization of cholinergic interneurons with afferent inputs, thus contributing to the loss of the pause response in Parkinson's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism*
  • Action Potentials / physiology*
  • Analysis of Variance
  • Animals
  • Anthracenes / pharmacology
  • Apamin / pharmacology
  • Ascorbic Acid / adverse effects
  • Barium / pharmacology
  • Computer Simulation
  • Corpus Striatum / injuries
  • Corpus Striatum / pathology*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Electric Stimulation / methods
  • In Vitro Techniques
  • Indoles / pharmacology
  • Interneurons / physiology*
  • Male
  • Models, Neurological
  • Neuroprotective Agents / pharmacology
  • Oxidopamine / adverse effects
  • Parkinsonian Disorders / chemically induced
  • Parkinsonian Disorders / pathology*
  • Pyridines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Substantia Nigra / injuries
  • Substantia Nigra / physiology

Substances

  • 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone
  • Anthracenes
  • Indoles
  • Neuroprotective Agents
  • Pyridines
  • Apamin
  • Barium
  • Oxidopamine
  • linopirdine
  • Acetylcholine
  • Ascorbic Acid