Local extracellular K<sup>+</sup> in cortex regulates norepinephrine levels, network state, and behavioral output.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37774097.
- Also identified by DOI 10.1073/pnas.2305071120 and PMC identifier 10556678.
- Licence recorded as CC BY-NC-ND.
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Abstract
Extracellular potassium concentration ([K<sup>+</sup>]<sub>e</sub>) is known to increase as a function of arousal. [K<sup>+</sup>]<sub>e</sub> is also a potent modulator of transmitter release. Yet, it is not known whether [K<sup>+</sup>]<sub>e</sub> is involved in the neuromodulator release associated with behavioral transitions. We here show that manipulating [K<sup>+</sup>]<sub>e</sub> controls the local release of monoaminergic neuromodulators, including norepinephrine (NE), serotonin, and dopamine. Imposing a [K<sup>+</sup>]<sub>e</sub> increase is adequate to boost local NE levels, and conversely, lowering [K<sup>+</sup>]<sub>e</sub> can attenuate local NE. Electroencephalography analysis and behavioral assays revealed that manipulation of cortical [K<sup>+</sup>]<sub>e</sub> was sufficient to alter the sleep-wake cycle and behavior of mice. These observations point to the concept that NE levels in the cortex are not solely determined by subcortical release, but that local [K<sup>+</sup>]<sub>e</sub> dynamics have a strong impact on cortical NE. Thus, cortical [K<sup>+</sup>]<sub>e</sub> is an underappreciated regulator of behavioral transitions.
Medical subject headings
- Norepinephrine
- Arousal