scholarly journals Taking the time for our bodies: How wearables can be used to assess circadian physiology

2021 ◽  
Vol 1 (4) ◽  
pp. 100067
Author(s):  
Md Mobashir Hasan Shandhi ◽  
Will Ke Wang ◽  
Jessilyn Dunn
Keyword(s):  
SLEEP ◽  
2021 ◽  
Vol 44 (Supplement_2) ◽  
pp. A40-A41
Author(s):  
Isabel Schöllhorn ◽  
Oliver Stefani ◽  
Manuel Spitschan ◽  
Robert Lucas ◽  
Christian Cajochen

Abstract Introduction Light emitted from visual displays can acutely increase alertness, improve cognitive performance and suppress melatonin in the evening. Here we tested the influence of different melanopic irradiance levels emitted by a metameric display setting on alertness, vigilance and salivary melatonin levels. Methods In an ongoing study, 37 healthy, male participants have so far completed a 2-week study protocol. Volunteers were assigned to one of four luminance groups which differed in brightness levels (27 cd/m2 - 280 cd/m2). Illuminance ranged between 7 and 85 lx. Within the four groups each volunteer was exposed to a low melanopic (LM) and a high melanopic condition (HM). The LM and HM differed in melanopic irradiance (ca. 3-fold change), but matched in terms of cone excitation (metamers). Before, during and after the light exposure, volunteers performed a psychomotor vigilance task (PVT). Subjective alertness and melatonin levels were continuously measured in half-hourly intervals throughout scheduled wakefulness in the 17-h in lab study. Results Preliminary analysis yielded an overall alerting response in the HM vs. the LM condition (p<0.05) concomitant with a trend of reduced melatonin levels in HM vs. LM (p=0.08). So far, we could not observe a difference in PVT performance for HM and LM (Reaction time responses between 100 and 500 ms). Since we are still lacking statistical power in the ongoing study, we cannot yet satisfactorily interpret interaction effects between melanopic condition and brightness. Conclusion Our data indicate that rather low brightness levels of high melanopic display light impacts alertness and melatonin levels in the evening. Thus, metameric low melanopic display light may be a promising method to attenuate activating properties of evening light on circadian physiology without affecting visual appearance. Support (if any) This project is funded by the Swiss National Science Foundation (SNSF).


Science ◽  
2016 ◽  
Vol 354 (6315) ◽  
pp. 1008-1015 ◽  
Author(s):  
Satchidananda Panda
Keyword(s):  

2021 ◽  
Vol 15 ◽  
Author(s):  
Atsushige Ashimori ◽  
Yasukazu Nakahata ◽  
Toshiya Sato ◽  
Yuichiro Fukamizu ◽  
Takaaki Matsui ◽  
...  

The circadian clock possesses robust systems to maintain the rhythm approximately 24 h, from cellular to organismal levels, whereas aging is known to be one of the risk factors linked to the alternation of circadian physiology and behavior. The amount of many metabolites in the cells/body is altered with the aging process, and the most prominent metabolite among them is the oxidized form of nicotinamide adenine dinucleotide (NAD+), which is associated with posttranslational modifications of acetylation and poly-ADP-ribosylation status of circadian clock proteins and decreases with aging. However, how low NAD+ condition in cells, which mimics aged or pathophysiological conditions, affects the circadian clock is largely unknown. Here, we show that low NAD+ in cultured cells promotes PER2 to be retained in the cytoplasm through the NAD+/SIRT1 axis, which leads to the attenuated amplitude of Bmal1 promoter-driven luciferase oscillation. We found that, among the core clock proteins, PER2 is mainly affected in its subcellular localization by NAD+ amount, and a higher cytoplasmic PER2 localization was observed under low NAD+ condition. We further found that NAD+-dependent deacetylase SIRT1 is the regulator of PER2 subcellular localization. Thus, we anticipate that the altered PER2 subcellular localization by low NAD+ is one of the complex changes that occurs in the aged circadian clock.


Biology ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 21
Author(s):  
Yool Lee ◽  
Jonathan P. Wisor

The circadian clock is a fundamental biological timing mechanism that generates nearly 24 h rhythms of physiology and behaviors, including sleep/wake cycles, hormone secretion, and metabolism. Evolutionarily, the endogenous clock is thought to confer living organisms, including humans, with survival benefits by adapting internal rhythms to the day and night cycles of the local environment. Mirroring the evolutionary fitness bestowed by the circadian clock, daily mismatches between the internal body clock and environmental cycles, such as irregular work (e.g., night shift work) and life schedules (e.g., jet lag, mistimed eating), have been recognized to increase the risk of cardiac, metabolic, and neurological diseases. Moreover, increasing numbers of studies with cellular and animal models have detected the presence of functional circadian oscillators at multiple levels, ranging from individual neurons and fibroblasts to brain and peripheral organs. These oscillators are tightly coupled to timely modulate cellular and bodily responses to physiological and metabolic cues. In this review, we will discuss the roles of central and peripheral clocks in physiology and diseases, highlighting the dynamic regulatory interactions between circadian timing systems and multiple metabolic factors.


2022 ◽  
pp. 074873042110597
Author(s):  
Nathan J. Klett ◽  
Olga Cravetchi ◽  
Charles N. Allen

Both inhibitory and excitatory GABA transmission exist in the mature suprachiasmatic nucleus (SCN), the master pacemaker of circadian physiology. Whether GABA is inhibitory or excitatory depends on the intracellular chloride concentration ([Cl−]i). Here, using the genetically encoded ratiometric probe Cl-Sensor, we investigated [Cl−]i in AVP and VIP-expressing SCN neurons for several days in culture. The chloride ratio (RCl) demonstrated circadian rhythmicity in AVP + neurons and VIP + neurons, but was not detected in GFAP + astrocytes. RCl peaked between ZT 7 and ZT 8 in both AVP + and VIP + neurons. RCl rhythmicity was not dependent on the activity of several transmembrane chloride carriers, action potential generation, or the L-type voltage-gated calcium channels, but was sensitive to GABA antagonists. We conclude that [Cl−]i is under circadian regulation in both AVP + and VIP + neurons.


2019 ◽  
pp. 31-41
Author(s):  
Sabra M. Abbott ◽  
Phyllis C. Zee
Keyword(s):  

2016 ◽  
Vol 230 (1) ◽  
pp. R1-R11 ◽  
Author(s):  
Anthony H Tsang ◽  
Mariana Astiz ◽  
Maureen Friedrichs ◽  
Henrik Oster

Endogenous circadian clocks regulate 24-h rhythms of behavior and physiology to align with external time. The endocrine system serves as a major clock output to regulate various biological processes. Recent findings suggest that some of the rhythmic hormones can also provide feedback to the circadian system at various levels, thus contributing to maintaining the robustness of endogenous rhythmicity. This delicate balance of clock–hormone interaction is vulnerable to modern lifestyle factors such as shiftwork or high-calorie diets, altering physiological set points. In this review, we summarize the current knowledge on the communication between the circadian timing and endocrine systems, with a focus on adrenal glucocorticoids and metabolic peptide hormones. We explore the potential role of hormones as systemic feedback signals to adjust clock function and their relevance for the maintenance of physiological and metabolic circadian homeostasis.


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