Nicotinic control of axon excitability regulates thalamocortical transmission

Nat Neurosci. 2007 Sep;10(9):1168-75. doi: 10.1038/nn1956. Epub 2007 Aug 19.

Abstract

The thalamocortical pathway, a bundle of myelinated axons that arises from thalamic relay neurons, carries sensory information to the neocortex. Because axon excitation is an obligatory step in the relay of information from the thalamus to the cortex, it represents a potential point of control. We now show that, in adult mice, the activation of nicotinic acetylcholine receptors (nAChRs) in the initial portion of the auditory thalamocortical pathway modulates thalamocortical transmission of information by regulating axon excitability. Exogenous nicotine enhanced the probability and synchrony of evoked action potential discharges along thalamocortical axons in vitro, but had little effect on synaptic release mechanisms. In vivo, the blockade of nAChRs in the thalamocortical pathway reduced sound-evoked cortical responses, especially those evoked by sounds near the acoustic threshold. These data indicate that endogenous acetylcholine activates nAChRs in the thalamocortical pathway to lower the threshold for thalamocortical transmission and to increase the magnitude of sensory-evoked cortical responses. Our results show that a neurotransmitter can modulate sensory processing by regulating conduction along myelinated thalamocortical axons.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acoustic Stimulation / methods
  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Action Potentials / radiation effects
  • Analysis of Variance
  • Animals
  • Axons / drug effects
  • Axons / physiology*
  • Cerebral Cortex / cytology
  • Cerebral Cortex / physiology*
  • Dihydro-beta-Erythroidine / pharmacology
  • Dose-Response Relationship, Radiation
  • Electric Stimulation / methods
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / physiology
  • Excitatory Postsynaptic Potentials / radiation effects
  • In Vitro Techniques
  • Mice
  • Neural Pathways / physiology
  • Neurons / cytology*
  • Neurons / drug effects
  • Nicotine / pharmacology
  • Nicotinic Agonists / pharmacology
  • Patch-Clamp Techniques / methods
  • Reaction Time / drug effects
  • Reaction Time / physiology
  • Reaction Time / radiation effects
  • Receptors, Nicotinic / physiology*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*
  • Synaptic Transmission / radiation effects
  • Thalamus / cytology
  • Thalamus / physiology*

Substances

  • Nicotinic Agonists
  • Receptors, Nicotinic
  • Dihydro-beta-Erythroidine
  • Nicotine