M1 muscarinic receptor modulation of Kir2 channels enhances temporal summation of excitatory synaptic potentials in prefrontal cortex pyramidal neurons

David B. Carr, D. James Surmeier*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

The cholinergic innervation of the prefrontal cortex (PFC) plays a pivotal role in regulating executive functions. Muscarinic receptors activated by acetylcholine depolarize pyramidal neurons in the rodent PFC homologue, but the mechanisms mediating this modulation are controversial. To address this question, we studied the responses of layer V rat pre- and infralimbic cortex pyramidal neurons to muscarinic receptor stimulation. Consistent with previous findings, M1 receptor stimulation produced a strong depolarization, leading to tonic firing. Voltage-clamp analysis revealed that M1 activation reduced constitutively active inwardly rectifying (Kir2) K + channel currents. Blocking protein kinase C activation or depleting intracellular Ca2+ stores did not affect the modulation. However, reversal of the modulation was prevented by the phosphoinositide kinase inhibitor, wortmanin, suggesting the modulation was mediated by depletions of membrane phosphatidylinositol-4,5-bisphosphate (PIP2). Reduction of Kir2 channel currents by M1 receptor stimulation significantly increased the temporal summation of excitatory synaptic potentials (EPSPs) evoked by repetitive stimulation of layer I. This action was complimented by M2/4 receptor mediated presynaptic inhibition of the same terminals. As a consequence of this dual modulation, the responses to a single, isolated afferent volley was reduced, but the response to a high-frequency afferent burst was potentiated.

Original languageEnglish (US)
Pages (from-to)3432-3438
Number of pages7
JournalJournal of neurophysiology
Volume97
Issue number5
DOIs
StatePublished - May 2007

ASJC Scopus subject areas

  • Neuroscience(all)
  • Physiology

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