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The KCNQ4-mediated M-current regulates the circadian rhythm in mesopontine cholinergic neurons
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Abstract
The M-current is a voltage gated potassium current inhibited by muscarinic activation and affected by several other G-protein coupled receptors. Its channels are formed by KCNQ subunits, from which KCNQ4 is restricted to certain brainstem structures. We sought evidence for the function of the M-current in the pedunculopontine nucleus (PPN) and the contribution of KCNQ4 subunits to the M-current and aimed to find its functional significance in the PPN. We found that cholinergic inputs of the PPN can effectively inhibit M-current. This current is capable of synchronizing neighboring neurons and inhibition of the M-current decreases neuronal synchronization. We showed that only a subpopulation of cholinergic neurons has KCNQ4-dependent M-current. The KCNQ4 subunit expression potentially regulates the presence of other KCNQ subunits. Deletion of KCNQ4 leads to alterations in adaptation of activity to light-darkness cycles, thus representing the potential role of KCNQ4 in regulation of sleep-wakefulness cycles. The presence of this protein restricted to certain brainstem nuclei raises the possibility that it might be a potential target for selective therapeutic interventions affecting the reticular activating system.
Title: The KCNQ4-mediated M-current regulates the circadian rhythm in mesopontine cholinergic neurons
Description:
Abstract
The M-current is a voltage gated potassium current inhibited by muscarinic activation and affected by several other G-protein coupled receptors.
Its channels are formed by KCNQ subunits, from which KCNQ4 is restricted to certain brainstem structures.
We sought evidence for the function of the M-current in the pedunculopontine nucleus (PPN) and the contribution of KCNQ4 subunits to the M-current and aimed to find its functional significance in the PPN.
We found that cholinergic inputs of the PPN can effectively inhibit M-current.
This current is capable of synchronizing neighboring neurons and inhibition of the M-current decreases neuronal synchronization.
We showed that only a subpopulation of cholinergic neurons has KCNQ4-dependent M-current.
The KCNQ4 subunit expression potentially regulates the presence of other KCNQ subunits.
Deletion of KCNQ4 leads to alterations in adaptation of activity to light-darkness cycles, thus representing the potential role of KCNQ4 in regulation of sleep-wakefulness cycles.
The presence of this protein restricted to certain brainstem nuclei raises the possibility that it might be a potential target for selective therapeutic interventions affecting the reticular activating system.
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