Abstract
The hyperpolarization-activated/cyclic nucleotide (HCN)-gated channels make important contributions to neural excitability. In prefrontal cortex, HCN channels are localized on the distal dendrites of layer V pyramidal neurons and decrease neural excitability when they are open. In the present study, using whole-cell voltage clamp recordings, the effect of an arousal peptide, orexin A, on HCN currents in layer V pyramidal neurons from mouse prelimbic cortex (PL), the homolog of the prefrontal cortex was investigated. The results demonstrated that orexin A suppressed HCN currents and shifted their activation curve to a more negative direction. This action of orexin A was blocked by SB334867, an orexin receptor 1 (OXR1) blocker and bisindolylmaleimide, a protein kinase C (PKC) inhibitor, indicating the involvement of OXR1 and PKC. The excitatory effect of orexin A on PL pyramidal neurons was enhanced when HCN currents were diminished, while attenuated when HCN currents were enlarged. In summary, orexin A inhibits HCN currents and enhances excitability of pyramidal neurons in PL, which may contribute to arousal and cognition.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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8-Bromo Cyclic Adenosine Monophosphate / pharmacology
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Animals
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Animals, Newborn
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Benzoxazoles / pharmacology
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Biophysics / methods
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Cerebral Cortex / cytology*
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Cyclic Nucleotide-Gated Cation Channels / antagonists & inhibitors
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Cyclic Nucleotide-Gated Cation Channels / metabolism*
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Dose-Response Relationship, Drug
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Drug Interactions
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Electric Stimulation / methods
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In Vitro Techniques
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Intracellular Signaling Peptides and Proteins / pharmacology*
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Membrane Potentials / drug effects
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Mice
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Mice, Inbred Strains
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Naphthyridines
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Neuropeptides / pharmacology*
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Neurotransmitter Agents / pharmacology*
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Orexin Receptors
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Orexins
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Patch-Clamp Techniques
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Pyramidal Cells / drug effects*
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Pyrimidines / pharmacology
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Receptors, G-Protein-Coupled / metabolism
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Receptors, Neuropeptide / metabolism
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Sodium Channel Blockers / pharmacology
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Tetrodotoxin / pharmacology
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Urea / analogs & derivatives
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Urea / pharmacology
Substances
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1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl urea
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Benzoxazoles
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Cyclic Nucleotide-Gated Cation Channels
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Intracellular Signaling Peptides and Proteins
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Naphthyridines
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Neuropeptides
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Neurotransmitter Agents
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Orexin Receptors
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Orexins
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Pyrimidines
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Receptors, G-Protein-Coupled
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Receptors, Neuropeptide
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Sodium Channel Blockers
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ICI D2788
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8-Bromo Cyclic Adenosine Monophosphate
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Tetrodotoxin
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Urea