Published July 21, 2023 | Version v1
Journal article Open

Pontine Waves Accompanied by Short Hippocampal Sharp Wave-Ripples During Non-rapid Eye Movement Sleep

  • 1. Department of Integrative Life Sciences, Graduate School of Life Sciences, Tohoku University, Sendai, Japan and Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai 980-, Japan
  • 2. Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai 980-, Japan
  • 3. Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK

Description

Ponto-geniculo-occipital or pontine (P) waves have long been recognized as an electrophysiological signature of rapid eye movement (REM) sleep. However, P-waves can be observed not just during REM sleep, but also during non-REM (NREM) sleep. Recent studies have uncovered that P-waves are functionally coupled with hippocampal sharp wave ripples (SWRs) during NREM sleep. However, it remains unclear to what extent P-waves during NREM sleep share their characteristics with P-waves during REM sleep and how the functional coupling to P-waves modulates SWRs. Here, we address these issues by performing multiple types of electrophysiological recordings and fiber photometry in both sexes of mice. P-waves during NREM sleep share their waveform shapes and local neural ensemble dynamics at a short (~100 milliseconds) timescale with their REM sleep counterparts. However, the dynamics of mesopontine cholinergic neurons are distinct at a longer (~10 seconds) timescale: although P-waves are accompanied by cholinergic transients, the cholinergic tone gradually reduces before P-wave genesis during NREM sleep. While P-waves are coupled to hippocampal theta rhythms during REM sleep, P-waves during NREM sleep are accompanied by a rapid reduction in hippocampal ripple power. SWRs coupled with P-waves are short-lived and hippocampal neural firing is also reduced after P-waves. These results demonstrate that P-waves are part of coordinated sleep-related activity by functionally coupling with hippocampal ensembles in a state-dependent manner.

Notes

This work was supported by Leverhulme Trust (RPG-2015377), Medical Research Council (MRC) (MR/V033964/1) and the European Union's Horizon 2020 (H2020-ICT, DEEPER, 101016787) to SS, and by the Japan Society for the Promotion of Science (JSPS) Postdoctoral Fellow for Research Abroad, a Research Fellowship from the Uehara Memorial Foundation, FOREST (JPMJFR2047) from Japan Science and Technology Agency and JSPS KAKENHI (20H05047) to TT.

Files

zsad193.pdf

Files (2.5 MB)

Name Size Download all
md5:0275b26b0abc9a0625d737d1358ea6ba
1.7 MB Preview Download
md5:72c2549af5cc8e904c6e731b77353093
846.6 kB Preview Download

Additional details

Related works

Is identical to
10.1093/sleep/zsad193 (DOI)

Funding

European Commission
DEEPER – DEEP BRAIN PHOTONIC TOOLS FOR CELL-TYPE SPECIFIC TARGETING OF NEURAL DISEASES 101016787