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Ionic Basis for Membrane Potential Resonance in Neurons of the Inferior Olive
Author(s) -
Yoshiko Matsumoto-Makidono,
Hisako Nakayama,
Miwako Yamasaki,
Taisuke Miyazaki,
Kazuto Kobayashi,
Masahiko Watanabe,
Masanobu Kano,
Kenji Sakimura,
Kouichi Hashimoto
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.06.053
Subject(s) - resonance (particle physics) , membrane potential , biophysics , chemistry , förster resonance energy transfer , neuroscience , ion channel , channel blocker , electrophysiology , biology , physics , biochemistry , receptor , fluorescence , atomic physics , organic chemistry , quantum mechanics , calcium
Some neurons have the ability to enhance output voltage to input current with a preferred frequency, which is called resonance. Resonance is thought to be a basis for membrane potential oscillation. Although ion channels responsible for resonance have been reported, the precise mechanisms by which these channels work remain poorly understood. We have found that resonance is reduced but clearly present in the inferior olivary neurons of Cav3.1 T-type voltage-dependent Ca(2+) channel knockout (KO) mice. The activation of Cav3.1 channels is strongly membrane potential dependent, but less frequency dependent. Residual resonance in Cav3.1 KO mice is abolished by a hyper-polarization-activated cyclic nucleotide-gated (HCN) channel blocker, ZD7288, and is partially suppressed by voltage-dependent K(+) channel blockers. Resonance is inhibited by ZD7288 in wild-type mice and impaired in HCN1 KO mice, suggesting that the HCN1 channel is essential for resonance. The ZD7288-sensitive current is nearly sinusoidal and strongly frequency dependent. These results suggest that Cav3.1 and HCN1 channels act as amplifying and resonating conductances, respectively.

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