The hyperpolarization-activated HCN4 channel is important for proper maintenance of oscillatory activity in the thalamocortical system

Zobeiri M., Chaudhary R., Blaich A., Rottmann M., Herrmann S., Meuth P., Bista P., Kanyshkova T., Lüttjohann A., Narayanan V., Hundehege P., Meuth S.G., Romanelli M.N., Urbano F.J., Pape H.C., Budde T., Ludwig A.

Research article (journal) | Peer reviewed

Abstract

Hyperpolarization-activated cation channels are involved, among other functions, in learning and memory, control of synaptic transmission and epileptogenesis. The importance of the HCN1 and HCN2 isoforms for brain function has been demonstrated, while the role of HCN4, the third major neuronal HCN subunit, is not known. Here we show that HCN4 is essential for oscillatory activity in the thalamocortical (TC) network. HCN4 is selectively expressed in various thalamic nuclei, excluding the thalamic reticular nucleus. HCN4-deficient TC neurons revealed a massive reduction of Ih and strongly reduced intrinsic burst firing, whereas the current was normal in cortical pyramidal neurons. In addition, evoked bursting in a thalamic slice preparation was strongly reduced in the mutant mice probes. HCN4-deficiency also significantly slowed down thalamic and cortical oscillations during active wakefulness. Taken together, these results establish that thalamic HCN4 channels are essential for the production of rhythmic intrathalamic oscillations and determine regular TC oscillatory activity during alert states.

Details about the publication

JournalCerebral cortex
Volume29
Issue5
Page range2291-2304
StatusPublished
Release year2019
Language in which the publication is writtenEnglish
DOI10.1093/cercor/bhz047
Link to the full texthttps://api.elsevier.com/content/abstract/scopus_id/85068538150
KeywordsIh; HCN4 knock out mice; HCN4 channels; thalamocortical oscillations; thalamocortical dysrhythmia

Authors from the University of Münster

Budde, Thomas
Institute of Physiology I (Neurophysiology)
Hundehege, Petra
Department for Neurology
Zobeiri, Mehrnoush
Institute of Physiology I (Neurophysiology)