Ruitong Jiang, Julian Low, Martha H Vitaterna, Karrie Fitzpatrick, Douglas J Weber, Darcy M Griffin
{"title":"Slow wave electroencephalogram spectral properties during adaptation of a new light dark cycle in cynomolgus monkeys.","authors":"Ruitong Jiang, Julian Low, Martha H Vitaterna, Karrie Fitzpatrick, Douglas J Weber, Darcy M Griffin","doi":"10.1093/sleepadvances/zpag020","DOIUrl":null,"url":null,"abstract":"<p><strong>Study objectives: </strong>Shifts in the light-dark cycle (L:D cycle) often trigger phase shifts in physiological data related to the sleep-wake cycle. Slow wave activity (delta) indicates sleep pressure and intensity. This study examines how delta power adapts to shifts in L:D cycle and the temporal dynamics of its coupling with rest-activity rhythms during re-entrainment.</p><p><strong>Methods: </strong>We collected electroencephalogram (EEG) and accelerometer data from three non-human primates during baseline and shifted (8-h delayed light-on) conditions. We derived delta power (0.5 ~ 4 Hz) using Fast Fourier Transform. To quantify changes in delta power dynamics following L:D cycle shifts, we calculated diurnal differences in delta power, per cent variance explained by time-of-day, circadian coupling with physical activity, and delta power activity transitions timing.</p><p><strong>Results: </strong>In both conditions, delta power exhibited a robust 24-h periodicity, and a significant portion of the variance (57.61% ± 6.99%) could be explained by time of day. We found an early transition of delta power in the first 2 days of the shifted condition, followed by realignment to the light-off time within 3 days after the shift. We used coherence analysis to reveal strong coupling between delta power and locomotor activity, with a consistent anti-phase relationship across baseline and phase shifted conditions.</p><p><strong>Conclusions: </strong>Our findings demonstrate that delta power adapts rapidly to environmental phase shifts while maintaining circadian rhythmicity and stable coordination with rest-activity rhythms. Here, we provide new insight into how neural and behavioral states remain aligned during circadian disruptions in a diurnal species.</p>","PeriodicalId":74808,"journal":{"name":"Sleep advances : a journal of the Sleep Research Society","volume":"7 1","pages":"zpag020"},"PeriodicalIF":0.0000,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13025076/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sleep advances : a journal of the Sleep Research Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/sleepadvances/zpag020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Study objectives: Shifts in the light-dark cycle (L:D cycle) often trigger phase shifts in physiological data related to the sleep-wake cycle. Slow wave activity (delta) indicates sleep pressure and intensity. This study examines how delta power adapts to shifts in L:D cycle and the temporal dynamics of its coupling with rest-activity rhythms during re-entrainment.
Methods: We collected electroencephalogram (EEG) and accelerometer data from three non-human primates during baseline and shifted (8-h delayed light-on) conditions. We derived delta power (0.5 ~ 4 Hz) using Fast Fourier Transform. To quantify changes in delta power dynamics following L:D cycle shifts, we calculated diurnal differences in delta power, per cent variance explained by time-of-day, circadian coupling with physical activity, and delta power activity transitions timing.
Results: In both conditions, delta power exhibited a robust 24-h periodicity, and a significant portion of the variance (57.61% ± 6.99%) could be explained by time of day. We found an early transition of delta power in the first 2 days of the shifted condition, followed by realignment to the light-off time within 3 days after the shift. We used coherence analysis to reveal strong coupling between delta power and locomotor activity, with a consistent anti-phase relationship across baseline and phase shifted conditions.
Conclusions: Our findings demonstrate that delta power adapts rapidly to environmental phase shifts while maintaining circadian rhythmicity and stable coordination with rest-activity rhythms. Here, we provide new insight into how neural and behavioral states remain aligned during circadian disruptions in a diurnal species.