Ultradian light-dark cycles in rodents are a precious tool to study the direct effects of repeated light exposures on sleep, in order to better understand the underlying mechanisms. This study aims to precisely evaluate the effects of light and dark exposures, according to circadian time, on sleep and waking distribution and quality, and to determine if these effects depend on the duration of light and dark pulses. To do this, mice were exposed to 24 h-long ultradian light-dark cycles with different durations of pulses: T2 cycle (1 h of light/1 h of dark) and T7 cycle (3.5 h of light/3.5 h of dark). Exposure to light not only promotes NREM and REM sleep and inhibits wake, but also drastically alters alertness and modifies sleep depth. These effects are modulated by circadian time, appearing especially during early subjective night, and their kinetics is highly dependent on the duration of pulses, suggesting that in the case of pulses of longer duration, the homeostatic process could overtake light direct influence for shaping sleep and waking distribution.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036312 | PMC |
http://dx.doi.org/10.3390/clockssleep4020019 | DOI Listing |
Curr Mol Med
December 2024
Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysuru 570015, Karnataka, India.
Rhythmicity is a characteristic feature of the inanimate universe. The organization of biological rhythms in time is an adaptation to the cyclical environmental changes brought on by the earth's rotation on its axis and around the sun. Circadian (L.
View Article and Find Full Text PDFEur J Neurosci
December 2024
Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
The suprachiasmatic nucleus (SCN) is the master clock that directly dictates behavioural rhythms to anticipate the earth's light/dark cycles. Although post-transcriptional regulators called microRNAs have been implicated in physiological SCN function, how the absence of the entire mature miRNome impacts SCN output has not yet been explored. To study the behavioural consequences of miRNA depletion in the SCN, we first generated a mouse model in which Dicer is inactivated in the SCN by crossing Syt10 mice with Dicer mice to study behavioural consequences of miRNA depletion in the SCN.
View Article and Find Full Text PDFNature
December 2024
Max Planck Institute for Brain Research, Frankfurt, Germany.
The mechanisms underlying the mammalian ultradian sleep rhythm-the alternation of rapid-eye-movement (REM) and slow-wave (SW) states-are not well understood but probably depend, at least in part, on circuits in the brainstem. Here, we use perturbation experiments to probe this ultradian rhythm in sleeping lizards (Pogona vitticeps) and test the hypothesis that it originates in a central pattern generator-circuits that are typically susceptible to phase-dependent reset and entrainment by external stimuli. Using light pulses, we find that Pogona's ultradian rhythm can be reset in a phase-dependent manner, with a critical transition from phase delay to phase advance in the middle of SW.
View Article and Find Full Text PDFHypertens Res
July 2024
Department of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
Artificial light at night (ALAN) disrupts 24-h variability of blood pressure, but the molecular mechanisms underlying these effects are unknown. Therefore, we analysed the daily variability of pulse pressure, the maximum value of acceleration rate of aortic pressure (dP/dt) measured by telemetry and protein expression in the thoracic aorta of normotensive male rats exposed to ALAN (1-2 lx) for 3 weeks. Daily, 24-h variability of pulse pressure and dP/dt was observed during a regular light/dark regimen with higher values during the dark compared to the light phase of the day.
View Article and Find Full Text PDFMol Metab
June 2024
Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA. Electronic address:
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!