A "sample-and-hold" pulse-counting integrator as a mechanism for graded memory underlying sensorimotor adaptation

Neuron. 2006 Feb 16;49(4):577-88. doi: 10.1016/j.neuron.2006.01.027.

Abstract

The mechanisms behind the induction of cellular correlates of memory by sensory input and their contribution to meaningful behavioral changes are largely unknown. We previously reported a graded memory in the form of sensorimotor adaptation in the electromotor output of electric fish. Here we show that the mechanism for this adaptation is a synaptically induced long-lasting shift in intrinsic neuronal excitability. This mechanism rapidly integrates hundreds of spikes in a second, or gradually integrates the same number of spikes delivered over tens of minutes. Thus, this mechanism appears immune to frequency-dependent fluctuations in input and operates as a simple pulse counter over a wide range of time scales, enabling it to transduce graded sensory information into a graded memory and a corresponding change in the behavioral output. This adaptation is based on an NMDA receptor-mediated change in intrinsic excitability of the postsynaptic neurons involving the Ca2+-dependent activation of TRP channels.

Publication types

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

MeSH terms

  • Acclimatization*
  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Action Potentials / radiation effects
  • Amino Acid Sequence
  • Animals
  • Behavior, Animal
  • Biological Clocks / physiology*
  • Calcium / metabolism
  • Calcium Channel Blockers / pharmacology
  • Dose-Response Relationship, Drug
  • Dose-Response Relationship, Radiation
  • Electric Fish
  • Electric Organ / drug effects
  • Electric Organ / physiology*
  • Electric Organ / radiation effects
  • Excitatory Amino Acid Agonists / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Flufenamic Acid / pharmacology
  • In Vitro Techniques
  • Medulla Oblongata / cytology
  • Memory / physiology*
  • Models, Neurological
  • N-Methylaspartate / pharmacology
  • Neurons / drug effects
  • Neurons / physiology*
  • Neurons / radiation effects
  • Physical Stimulation / methods
  • Piperazines / pharmacology
  • TRPM Cation Channels / antagonists & inhibitors
  • TRPM Cation Channels / metabolism
  • omega-Conotoxin GVIA / pharmacology

Substances

  • Calcium Channel Blockers
  • Excitatory Amino Acid Agonists
  • Excitatory Amino Acid Antagonists
  • Piperazines
  • TRPM Cation Channels
  • Flufenamic Acid
  • N-Methylaspartate
  • omega-Conotoxin GVIA
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
  • Calcium