Year: 2008
Type: article
Abstract: 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.
Author: Jonas Dyhrfjeld-Johnsen
Institution: University of California, Irvine
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,801
OpenAlex ID: W2040940307