Upregulated H-current in hyperexcitable CA1 dendrites after febrile seizures

Somatic recordings from CA1 pyramidal cells indicated a persistent upregulation of the h-current (I(h)) after experimental febrile seizures. Here, we examined febrile seizure-induced long-term changes in I(h) and neuronal excitability in CA1 dendrites. Cell-attached recordings showed that dendritic...

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Bibliographic Details
Published in:Frontiers in cellular neuroscience 2008, Vol.2, p.2-2
Main Authors: Dyhrfjeld-Johnsen, Jonas, Morgan, Robert J, Földy, Csaba, Soltesz, Ivan
Format: Article
Language:English
Subjects:
Action potential
Cell culture
Convulsions & seizures
Dendrite
Dendrites
Depolarization
Epilepsy
Excitability
Fever
Gene expression
h-current
Hyperthermia
Kinases
Membrane potential
Neurons
Neuroscience
Neurosciences
Pyramidal cells
Seizures
Sucrose
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Summary:Somatic recordings from CA1 pyramidal cells indicated a persistent upregulation of the h-current (I(h)) after experimental febrile seizures. Here, we examined febrile seizure-induced long-term changes in I(h) and neuronal excitability in CA1 dendrites. Cell-attached recordings showed that dendritic I(h) was significantly upregulated, with a depolarized half-activation potential and increased maximal current. Although enhanced I(h) is typically thought to be associated with decreased dendritic excitability, whole-cell dendritic recordings revealed a robust increase in action potential firing after febrile seizures. We turned to computational simulations to understand how the experimentally observed changes in I(h) influence dendritic excitability. Unexpectedly, the simulations, performed in three previously published CA1 pyramidal cell models, showed that the experimentally observed increases in I(h) resulted in a general enhancement of dendritic excitability, primarily due to the increased I(h)-induced depolarization of the resting membrane potential overcoming the excitability-depressing effects of decreased dendritic input resistance. Taken together, these experimental and modeling results reveal that, contrary to the exclusively anti-convulsive role often attributed to increased I(h) in epilepsy, the enhanced I(h) can co-exist with, and possibly even contribute to, persistent dendritic hyperexcitability following febrile seizures in the developing hippocampus.
ISSN:1662-5102
1662-5102
DOI:10.3389/neuro.03.002.2008