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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.