Enhanced neuronal excitability in rat CA1 pyramidal neurons following trace eyeblink conditioning acquisition is not due to alterations in I M

Neurobiol Learn Mem. 2008 Feb;89(2):125-33. doi: 10.1016/j.nlm.2007.07.002. Epub 2007 Aug 20.

Abstract

Previous work done by our laboratory has demonstrated a reduction of the post-burst afterhyperpolarization (AHP) and accommodation following trace eyeblink conditioning in rabbit CA1 pyramidal neurons. Our laboratory has also demonstrated a reduction in the AHP in rat CA1 pyramidal neurons following spatial learning. In the current study we have extended our findings in rabbits by showing a reduction in both the AHP and accommodation in F344 X BN rat CA1 pyramidal neurons following acquisition of trace eyeblink conditioning. A component current of the AHP, I(M), was evaluated with a specific blocker of this current, and showed no apparent contribution to the learning-related increase in neuronal excitability. Rather, a reduction in an isoproterenol-sensitive component of the AHP, presumably sI(AHP), was observed to underlie the learning-specific change.

Publication types

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

MeSH terms

  • Action Potentials / drug effects*
  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Arousal / drug effects*
  • Blinking / drug effects*
  • Conditioning, Psychological / drug effects*
  • Electromyography
  • Hippocampus / drug effects
  • Isoproterenol / administration & dosage
  • Isoproterenol / pharmacology*
  • Male
  • Neurons / drug effects*
  • Patch-Clamp Techniques
  • Potassium Channels, Calcium-Activated / metabolism*
  • Pyramidal Cells / drug effects*
  • Rats
  • Rats, Inbred F344

Substances

  • Adrenergic beta-Agonists
  • Potassium Channels, Calcium-Activated
  • Isoproterenol