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Sleep Sci. 2015 Apr-Jun;8(2):92-9. doi: 10.1016/j.slsci.2015.06.002. Epub 2015 Jul 10.

Pedunculopontine arousal system physiology - Implications for insomnia.

Sleep science (Sao Paulo, Brazil)

Edgar Garcia-Rill, Brennon Luster, Susan Mahaffey, Veronica Bisagno, Francisco J Urbano

Affiliations

  1. Center for Translational Neuroscience, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  2. IFIBYNE-CONICET and ININFA-CONICET, University of Buenos Aires, Argentina.

PMID: 26483950 PMCID: PMC4608886 DOI: 10.1016/j.slsci.2015.06.002

Abstract

We consider insomnia a disorder of waking rather than a disorder of sleep. This review examines the role of the reticular activating system, especially the pedunculopontine nucleus, in the symptoms of insomnia, mainly representing an overactive waking drive. We determined that high frequency activity during waking and REM sleep is controlled by two different intracellular pathways and channel types in PPN cells. We found three different PPN cell types that have one or both channels and may be active during waking only, REM sleep only, or both. These discoveries point to a specific mechanism and novel therapeutic avenues for insomnia.

Keywords: CaMKII, calcium/calmodulin-dependent protein kinase; Calcium channels; EEG, electroencephalogram; Gamma band activity; KA, kainic acid; N-type calcium channel; NCS-1, neuronal calcium sensor protein 1; NMDA, n methyl d aspartic acid; Neuronal calcium sensor protein; P/Q-type calcium channel; PGO, ponto-geniculo-occipital; PPN, pedunculopontine nucleus; RAS, reticular activating system; REM, rapid eye movement; SWS, slow wave sleep; cAMP, cyclic adenosine monophosphate; ω-Aga, ω-agatoxin-IVA; ω-CgTx, ω-conotoxin-GVIA

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