Breathing‐evoked potentials in humans during wakefulness and sleep
Breathing modulates cortical activities and cognitive functions, but the neurophysiological basis of the brain-breathing relationship is incompletely understood. We aimed to determine whether breathing at rest evokes scalp EEG-detectable potentials (as inspiratory occlusions do in the respiratory-related evoked potential model), whether these signatures persist during sleep and whether they are linked to sleep-organizing processes. We examined recordings from 729 participants in the Cleveland Family Study to identify cortical activity time-locked to inspiration during wakefulness and sleep, with a median of 7871 respiratory cycles analysed per participant. Breathing-related cortical responses were assessed in the time and frequency domains. Quiet breathing evoked a reproducible sequence of cortical potentials during wakefulness, including a pre-inspiratory component ∼300 ms before inspiration and several post-inspiratory peaks ≤3 s after. These responses persisted during non-rapid eye movement stages 2 and 3 (N2 and N3) and rapid eye movement (REM) sleep, in which they showed simplified morphology resembling K-complexes and co-occurred with increased spindle-range activity. The pattern was present irrespective of body mass index and was qualitatively unchanged in the 203 participants free of sleep-disordered breathing, arguing against obesity or sleep apnoea as its origin. Scalp EEG can detect breathing-evoked potentials during quiet breathing in awake humans. These potentials persist during sleep with a morphology that resembles cortical activities previously associated with sleep stabilization. Further studies are needed to determine the physiological and clinical significance of these observations in health and disease. KEY POINTS: Spontaneous breathing at rest evokes reproducible breathing-related cortical potentials detectable with scalp EEG. These potentials persist during sleep. They are associated with time-locked modulation of cortical oscillatory activity.
Authors
- Thomas Similowski (ORCID: https://orcid.org/0000-0003-2868-9279)
- L. Grassion (ORCID: https://orcid.org/0000-0002-1909-9755)
- Marie‐Cécile Nierat (ORCID: https://orcid.org/0000-0001-9370-7301)
- Delphine Oudiette (ORCID: https://orcid.org/0000-0002-6598-4130)
- Jésus Gonzalez‐Bermejo (ORCID: https://orcid.org/0000-0003-2395-4694)
- Maxime Patout (ORCID: https://orcid.org/0000-0002-1366-8726)
- Nicolas Wattiez (ORCID: https://orcid.org/0000-0002-2344-7660)
- Isabelle Arnulf (ORCID: https://orcid.org/0000-0002-2240-2516)
- Thomas Andrillon (ORCID: https://orcid.org/0000-0003-2794-8494)
- Jessica Njlagni Voutsa
Institutions
- Centre National de la Recherche Scientifique (FR)
- Inserm (FR)
- Sorbonne Université (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
- Hôpital Cardiologique du Haut-Lévêque (FR)
- Pitié-Salpêtrière Hospital (FR)
- Institut du Cerveau (FR)
Publication Details
- Journal
- The Journal of Physiology
- Published
- 2026-10-28
- DOI
- https://doi.org/10.1113/jp290737
- Primary Topic
- Neuroscience of respiration and sleep
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Université de Bordeaux
- National Institutes of Health
- European Research Council
- National Heart, Lung, and Blood Institute