Learning-induced reduction in post-burst after-hyperpolarization (AHP) is mediated by activation of PKC

Eur J Neurosci. 2002 Sep;16(5):965-9. doi: 10.1046/j.1460-9568.2002.02155.x.


We studied the role of protein kinase C (PKC) and protein kinase A (PKA) in mediating learning-related long lasting reduction of the post-burst after-hyperpolarization (AHP) in cortical pyramidal neurons. We have shown previously that pyramidal neurons in the rat piriform (olfactory) cortex from trained (TR) rats have reduced post-burst AHP for 3 days after odour-discrimination learning, and that this reduction is due to decreased conductance of calcium-dependent potassium current. In the present study, we examined whether this long-lasting reduction in AHP is mediated by second messenger systems. The broad-spectrum kinase inhibitor, H7, increased the AHP in neurons from TR rats, but not in neurons from pseudo-trained (pseudo-TR) and naive rats. Consequently, the difference in AHP amplitude between neurons from TR and control animals was diminished. This effect was also obtained by application of the specific PKC inhibitor, GF-109203x. The PKC activator, 1-Oleoyl-2-acetyl-sn-glycerol (OAG), significantly reduced the AHP in neurons from naive and pseudo-TR rats, but not in neurons from TR rats, so that the difference between the groups was abolished. The PKA-specific inhibitor, H-89, increased the AHP in neurons from all groups to a similar extent, and the difference in AHP amplitude between neurons from TR rats and neurons from controls was maintained. We suggest that while the post-burst AHP in piriform cortex pyramidal neurons is modulated by both PKC and PKA, a PKC-dependent process maintains the learning-related reduction of the AHP in these cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials*
  • Animals
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / physiology*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Electrophysiology
  • Learning / physiology*
  • Male
  • Membrane Potentials
  • Odorants
  • Protein Kinase C / metabolism*
  • Pyramidal Cells / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Second Messenger Systems
  • Smell / physiology


  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C