Robust switches in thalamic network activity require a timescale separation between sodium and T-type calcium channel activations
Author(s) -
Kathleen Jacquerie,
Guillaume Drion
Publication year - 2021
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1008997
Subject(s) - neuroscience , neuromodulation , sodium channel , t type calcium channel , synaptic plasticity , robustness (evolution) , computer science , conductance , calcium , voltage dependent calcium channel , chemistry , physics , stimulation , biology , sodium , receptor , biochemistry , organic chemistry , condensed matter physics , gene
Switches in brain states, synaptic plasticity and neuromodulation are fundamental processes in our brain that take place concomitantly across several spatial and timescales. All these processes target neuron intrinsic properties and connectivity to achieve specific physiological goals, raising the question of how they can operate without interfering with each other. Here, we highlight the central importance of a timescale separation in the activation of sodium and T-type calcium channels to sustain robust switches in brain states in thalamic neurons that are compatible with synaptic plasticity and neuromodulation. We quantify the role of this timescale separation by comparing the robustness of rhythms of six published conductance-based models at the cellular, circuit and network levels. We show that robust rhythm generation requires a T-type calcium channel activation whose kinetics are situated between sodium channel activation and T-type calcium channel inactivation in all models despite their quantitative differences.
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