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Zeitzer, J. M.

Publications and source records attributed to Zeitzer, J. M..

2 recordsLinked to original sources

Simultaneous stomach-brain electrophysiology reveals dynamic coupling in human sleep

Sleep involves coordinated interactions between the brain and body, yet whether and how peripheral physiology is organized during human sleep is poorly understood. Because gastric rhythms are strongly modulated by arousal states during wakefulness, we hypothesized that gastric electrical rhythms exhibit structured dynamics aligned with cortical oscillations during sleep. Using simultaneous high-density electroencephalography and electrogastrography, we find that gastric activity persists throughout sleep, increases during non-rapid eye movement (NREM), and exhibits infraslow fluctuations that are amplified during NREM. Moreover, gastric activity is synchronized with slow oscillations and sleep spindles, with gastric power tracking spindle occurrence and cortical infraslow cycles. Stomach-brain coupling predicted next-day memory recall beyond cortical measures, whereas gastric infraslow dynamics predicted subjective sleep quality beyond polysomnographic measures. Together, our findings show that even as the brain disconnects from the external world, it maintains structured communication with peripheral organs, reframing sleep as a coordinated, multi-organ physiological state.

neuroscience↗

Duration invariance of the human circadian system response to pulsed light

The melanopsin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs) are characterised by a delayed off-time following light offset. Here, we exploited this unusual physiologic property to characterise the exquisite sensitivity of the human circadian system to flashed light. In a 34-hour in-laboratory between-subjects design, we examined variable-intensity (3-9500 photopic lux; n=28 participants) full-field flashes at fixed duration (2 ms), and variable-duration (10 s-10 s) full-field flashes at fixed intensity (2000 photopic lux; n=31 participants) delivered using eye masks. We measured the circadian phase shift of the dim-light melatonin onset (DLMO) on the subsequent evening, acute melatonin suppression, objective alertness, and subjective sleepiness during the flash sequence. We find a clear dose-response relationship between flash intensity and the induced circadian phase shift, with an approximate increase of 10 minutes of phase delay for each ten-fold increase in photopic illuminance, but no parametric relationship between flash duration and induced circadian phase shift.

neuroscience↗