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Dendritic Ih ensures high-fidelity dendritic spike responses of motion-sensitive neurons in rat superior colliculus

J Neurophysiol. 2008 May;99(5):2066-76. doi: 10.1152/jn.00556.2007. Epub 2008 Jan 23.

Abstract

Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels that generate I(h) currents are widely distributed in the brain and have been shown to contribute to various neuronal functions. In the present study, we investigated the functions of I(h) in the motion-sensitive projection neurons [wide field vertical (WFV) cells] of the superior colliculus, a pivotal visual center for detection of and orientating to salient objects. Combination of whole cell recordings and immunohistochemical investigations suggested that HCN1 channels dominantly contribute to the I(h) in WFV cells among HCN isoforms expressed in the superficial superior colliculus and mainly located on their expansive dendritic trees. We found that blocking I(h) suppressed the initiation of short- and fixed-latency dendritic spike responses and led instead to long- and fluctuating-latency somatic spike responses to optic fiber stimulations. These results suggest that the dendritic I(h) facilitates the dendritic initiation and/or propagation of action potentials and ensures that WFV cells generate spike responses to distal synaptic inputs in a sensitive and robustly time-locked manner, probably by acting as continuous depolarizing drive and fixing dendritic membrane potentials close to the spike threshold. These functions are different from known functions of dendritic I(h) revealed in hippocampal and neocortical pyramidal cells, where they spatiotemporally limit the propagations of synaptic inputs along the apical dendrites by reducing dendritic membrane resistance. Thus we have revealed new functional aspects of I(h), and these dendritic properties are likely critical for visual motion processing in these neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Cardiotonic Agents / pharmacology
  • Cyclic Nucleotide-Gated Cation Channels / drug effects
  • Cyclic Nucleotide-Gated Cation Channels / physiology*
  • Data Interpretation, Statistical
  • Dendrites / drug effects
  • Dendrites / physiology*
  • Electrophysiology
  • Excitatory Postsynaptic Potentials / drug effects
  • Fiber Optic Technology
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Immunohistochemistry
  • In Situ Hybridization
  • Membrane Potentials / physiology
  • Motion Perception / drug effects
  • Motion Perception / physiology*
  • Photic Stimulation
  • Potassium Channels / drug effects
  • Potassium Channels / physiology*
  • Pyrimidines / pharmacology
  • Rats
  • Rats, Long-Evans
  • Rats, Wistar
  • Superior Colliculi / cytology
  • Superior Colliculi / drug effects
  • Superior Colliculi / physiology*
  • Synapses / drug effects
  • Synapses / physiology
  • Synaptic Membranes / drug effects
  • Synaptic Membranes / physiology

Substances

  • Cardiotonic Agents
  • Cyclic Nucleotide-Gated Cation Channels
  • Hcn1 protein, rat
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Potassium Channels
  • Pyrimidines
  • ICI D2788